The authors are grateful to Jeremy C. M. Teo and S. Ryan Oliver for their contribution and Jolanta Kilarska for help in image processing. We thank the BIOP core facility at EPFL for the support with two-photon microscopy
This work was supported in part by grants from the European Research Commission (DC-Lymph, 206653-2), the European Framework Project 7 (AngioScaff), the Swiss National Science Foundation (31-135756), and the U.S. National Institutes of Health (NIH)/NIH Heart, Lung, and Blood Institute (NHLBI) (RO1 HL096539). Additionally, funds from the Robert Wenner Award (Swiss Cancer League) allowed the purchase the Leica stereomicroscope used in this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

All procedures performed on animals were in strict accordance with the Swiss Animal Protection Act, the ordinance on animal protection and the ordinance on animal experimentation. We confirm that our Institutional Animal Care and Use Committee (IACUC), named Commission de Surveillance de l'Etat de Vaud (Permit Number: 2687), specifically approved this study.
1. Tumor Inoculation of the Ear
<ol>
	<li>Culture B16-F10-GFP melanoma cells in a 10 cm Petri dish using DMEM + 10% FBS media.</li>
	<li>When the cells are 80-90% confluent, wash them with PBS and detach them by trypsinization. Spin down cells at 1,500 x g for 5 min at 4 &#176;C, resuspend the pellet in 1 ml Ringer's solution and transfer it into a 1.5 ml Eppendorf tube. Spin again and remove all supernatant except a thin layer of medium that stays just above the pellet. Resuspend the cells to end up with a thick cell slurry.</li>
	<li>Anesthetize the mouse with a mixture of ketamine/dorbene [medetomidine] (75mg/kg-1mg/kg) and confirm that the animal is sufficiently anesthetized by performing a gentle toe pinch. Increase the isoflurane concentration in steps of 0.1 % in case movements are observed (e.g. withdrawal of the paw). Keep mouse on a rectal thermistor controlled heating pad (37 &#176;C) during the whole procedure and protect its eyes with an appropriate ophthalmic ointment.</li>
	<li>Prepare a Hamilton syringe (33 G needle, 10 ml syringe volume). Remove the tip cap with the needle and load 20 &#181;l of cell slurry on top of the tip chamber. Pull back the plunger until 5 ml slurry is loaded inside the syringe. Remove the excess slurry from the tip chamber and close the tip cap.</li>
	<li>Using adhesive tape, fix the proximal edge of the ear on the tip of an index finger. In a 45&#176; angle, slowly insert the Hamilton syringe needle between dorsal dermis and the cartilage. Once inside, penetrate the ear proximal to distal for about 2-3 mm. 
	Note: The procedure of cell injection should be done by trained and certified technician. In addition this process must be perform slowly and in sequence: first the needle should be placed horizontally to the ear skin and inserted slowly into the ear dermis. Once and only then the needle end is in the skin, the plunger should be pressed. Pressing of the plunger will initiate cells inoculation in the skin. In the unlikely event of the needle passing the two layers of the ear dermis, the layer of the cartilage and enters the skin of the person performing the experiment, the pain inflicted to the experimentator finger should be considered as an alarming sign and cause immediate retraction of the needle from the experimentator skin. In that case plunger should not be pressed and skin should be sterilized with alcohol. Alternatively, inanimate object instead of a finger can be used to stabilize the ear.</li>
	<li>Inject 3 &#181;l cell slurry and slowly retract the needle from the ear. Let tumor cells form a solid tumor during 7-9 days and follow the tumor growth by using a fluorescence stereomicroscope.</li>
	<li>Alternatively, to follow the early steps of tumor cell interaction with tissue matrix, apply 50 &#956;l of 100,000 tumor cells suspended in Ringer's solution on the exposed and stained ear dermis (after step 3.3).</li>
</ol>
2. Ear Surgery
<ol>
	<li>Three days before the experiment, shave the mouse head, depilate the hairs around the head and ear (10-15 sec) and rinse with water.</li>
	<li>Anesthetize the mouse with a mixture of humidified oxygen and isoflurane (3-4% induction, 1-2% maintenance) and confirm that the animal is sufficiently anesthetized by performing a gentle toe pinch. Increase the isoflurane concentration in steps of 0.1% in case movements are observed (e.g. withdrawal of the paw). Keep mouse on a rectal thermistor controlled heating pad (37 &#176;C) during the whole procedure and protect its eyes with an appropriate ophthalmic ointment.</li>
	<li>Build a platform made out of 8 glued glass histology slides. Turn the mouse on its back and gently place the tumor-bearing ear on the stack of glass slides. Use small stripes of adhesive tape to fixate the anterior and posterior edges of the ear to the stack.</li>
	<li>Cut the ventral skin of the ear along the antihelix of the mouse pinna using a scalpel. With the help of curved tweezers, gently peel off the ventral dermis and the cartilage from the dorsal dermis where the tumor was inoculated. Pull off the ventral skin and cartilage with curved forceps, exposing the dorsal dermis. NOTE: If the major vessels of the ear are cut or the blood circulation does not return to normal flow within 15 min, the ear cannot be used for imaging. Always keep the opened ear skin wet by using Ringer's buffer and protect the humidity by using a coverslip.</li>
	<li>In case there is persistent bleeding form tumor vessels, stop the bleeding by adding 100 &#181;l thrombin (5 U/ml) in Ringer&#39;s buffer (102 mM NaCl, 5 mM KCl, 2 mM CaCl2, 28 mM sodium lactate) on top of the ear for 5 min.</li>
	<li>Wash the ear twice with approximately 5 ml of Ringer's buffer and remove extra liquid with sterile wipes. Immediately proceed to the next step (do not let the open ear dry at any point!).</li>
</ol>
3. Immunofluorescence Staining
Use Ringer&#39;s buffer supplemented with human serum (1:10), mouse polyclonal secondary antibody to human IgG (1:50), and 125 IU/ml (2.5 mg/ml) aprotinin (blocking buffer) for all staining steps. Aprotinin inhibits plasmin promoting coagulation to limit initial bleeding that may occur after surgery.
<ol>
	<li>Fold the part of the ear with the open dermis into the eminentia conchae and dry the outer unopened ear dermis with sterile wipes. Immobilize the ear on the stack of glass slide by applying 0.5 &#956;l of surgical glue to the anterior and posterior dorsal edges. Then, gently flatten the dorsal ear dermis onto the glass.</li>
	<li>Apply primary antibodies targeting extracellular matrix molecules at a concentration of 10 &#181;g/ml in a total volume of 100 &#181;l blocking buffer to the exposed ear. Cover the ear with a cover slip in order to prevent the staining solution to dry on the ear edges. Incubate for 15 min. Wash the ear twice with approximately 5 ml of Ringer's buffer.</li>
	<li>Apply appropriate secondary antibodies or streptavidin conjugates (fluorophores with a high excitation wavelength such as 594 nm or 647 nm are favorable for intravital imaging) at a concentration of 10 &#181;g/ml in a total volume of 100 &#181;l blocking buffer to the exposed ear. Cover the ear with a cover slip and incubate for 15 min. Wash the ear twice with approximately 5 ml of Ringer's buffer.</li>
</ol>
4. Interaction of Blood-borne Activated Splenocytes with Tumor Cells in situ
<ol>
	<li>7 days after inoculation of GFP-B16-F10 melanoma on the back skin of congenic mouse, euthanize the animal and collect spleens. Isolate splenocytes with mechanical disruption of the spleen through a 70 &#956;m cell strainer.</li>
	<li>Label splenocytes for 8 min at 37 &#176;C with Red CMTPX cell cytoplasm stain (1 &#956;M in PBS), wash 4 times in 15 ml at 4 &#176;C and immediately inject with 200 &#956;l serum free medium into the tail vein of mouse whose ears were inoculated with B16-F10- GFP 7 days earlier.</li>
</ol>
5. Intravital Imaging by Using a Stereomicroscope
<ol>
	<li>For short-term imaging (up to 2 hr), add freshly prepared sterile ascorbate-Ringer's buffer containing 140 mM sodium ascorbate, 10 mM HEPES, 4 mM KCl and 5 mM CaCl2, at a pH of 7.5 (ascorbate-Ringer's buffer final osmolarity 320 mOsM) on top of the immobilized ear. Cover the ear with a coverslip and start imaging by using a fluorescence stereomicroscope with 2X lens.</li>
	<li>For long-term imaging (more than 2 hr), place the outlet of a needle (connected to a reservoir containing ascorbate-Ringer's buffer) under the coverslip, about 0.5 cm away from the ear. Use a peristaltic pump at a speed of 1 &#181;l/min to constantly deliver ascorbate-Ringer's buffer to the chamber under the coverslip.</li>
	<li>Change the 1X lens (working distance 6 cm) to 2X lens (working distance 2 cm). Open the acquisition software and configure the settings of the fluorescent stereomicroscope. In camera settings choose 12 bit as the image color depth and adjust the camera range of grey-scale values from 0% (minimum) to 5.1% (maximum) and set gamma correction to 2.
	<ol>
		<li>Set acquisition gain to 1 (minimum), fluorescence intensity to 1,000 (maximum), magnification set to 280X-320X and adjust the exposure time avoiding over- or under- exposure (exposure time should be less than 1 sec). Depending on the number of imaging fields (usually 10 to 20), time interval for acquisition cycle should be set between 1 to 2 min. Shorten times may cause the bleaching and phototoxicity.</li>
	</ol>
	</li>
	<li>Choose several fields that contain tumor cells as well as stained ECM proteins (such as in Figure 3). Using the motorized stage, acquire images of the appropriate fluorescent channels (such as GFP and fluorophore 647 in Figure 3) over time (e.g. every 2 min).</li>
	<li>After the experiment, euthanize the mouse according to institutional animal guidelines. In this case, at the end of the experiment, euthanize the anesthetized mouse by cervical dislocation followed by exsanguination (intracardiac perfusion).</li>
</ol>
6. Intravital Imaging by Using a Multiphoton Microscope
<ol>
	<li>Using silicon grease, build a circular wall of about 2 cm diameter and 2-3 mm height around the ear, starting at the base of the ear. Make sure there are no leaking points. Fill the circle with ascorbate-Ringer's buffer.</li>
	<li>Place mouse on the stage and connect the heating pad (37 &#176;C).</li>
	<li>Open acquisition software and configure the settings of the multiphoton microscope.</li>
	<li>Choose up to four different fields that contain tumor cells and stained ECM proteins (such as in Figure 3). In this example, tune the Ti-Saphire laser to 850 nm for GFP signal a subsequent single photon 647 for fluorophore 647 staining and visualize fibrillar collagens with SHG. Acquire images of the appropriate fluorescent channels (such as GFP and fluorophore 647 in Figure 3) and second harmonic generation over time, e.g. every 2 min, with water immersion HCX APO 20X with 1.00 NA lens and 2 mm working distance.</li>
	<li>After the experiment, euthanize anesthetized mouse with cervical dislocation followed by exsanguination (intracardiac perfusion).</li>
</ol>

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The authors have nothing to disclose.

Significance
Here we present a novel intravital microscopy approach that allows high resolution and dynamic visualization of different tissue microenvironment components, including fibrillar as well as mesh-like matrix proteins. This method has several advantages over current intravital imaging techniques: (i) Intravital fluorescence imaging has been used in microcirculation studies, e.g., to track solute leakage from blood or into lymphatics, but has not been combined with immunostaining. (ii) The use of genetically modified reporter mice allows for specific cell types to be imaged, but requires their availability (or substantial effort to create new ones) and limits the number of interacting cell types that can be studied. (iii) Extracellular matrix can be imaged in vivo using second harmonic generation, but this technique can only detect fibrous collagens, leaving a large number of important extracellular components such as basement membranes, fibronectins, tenascins, growth factors, chemokines and tissue glycosaminoglycans out of reach for current research. Our method overcomes these limitations, and allows standard imaging techniques to be incorporated and further combined with immunostainings for other cell types, tissue structures, deposits of heparin sulfate binding growth factors (e.g. VEGF26) and chemokines (CCL215,18and Fig. 2D), or extracellular matrix proteins while simultaneously tracking blood and/or lymphatic flows.
Limitations
The epifluorescence imaging of intravital IF is limited to the thin skin flaps, deprived of thick hypodermis (adipose tissue). While we found that the dorsal ear dermis is optimal for relatively harmless surgical exposition of the ear skin, epifluorescence with intravital IF technique is not limited to ear dermis and could potentially be applied to e.g. the exposed skin of the toes or the back skin of the newborn mouse. Rapid antibody staining (15 minutes) in immunofluorescence IF is not dependent on passive diffusion but requires functional lymphatic drainage and interstitial fluid flow, hence no staining can be observed if lymphatic vessels are occluded27. In line with that, lymphatic vessels stain stronger then leaky blood vasculature (injured vessels, arterioles)5. The separation of the dorsal and ventral ear skin flaps is a mild surgical procedure but it causes injury to some capillaries and cell death to various tissue cells. This might be a problem when one needs to investigate completely intact tissue, e.g. looking at the mild effect of drugs on cell survival. Also the application of antioxidant that serves to protect the skin from phototoxicity and photobleaching excludes the use of intravital immunofluorescence technique to study e.g. the tissue oxidative stress or nitric oxide biology.
Finally, blinding of tissue resident macrophages with immune complexes can activate these cells and influence e.g. the study of tissue immune response and dendritic cell activation.
Modifications and troubleshooting
In order to study tissue oxidative stress or nitric oxide biology, ascorbate has to be replaced with other tissue compatible media that does not interfere with the experimental output. Similarly, blocking Fc receptors on dermal immune cells should be avoided if the goal of the study is the function and activation of the tissue immune response and dendritic cell activation and migration. This can be done with the use of secondary antibody with Fc fragment cleaved (F(ab)2 antibody fragments) or the use of biotinylated antibody and fluorescent streptavidin as detection reagents.
Future applications
We present a novel and unique intravital IF technique to image non-fibrillar components of extracellular matrix in transplantable skin tumors in combination with SHG-detected fibrillar and matured collagens using two-photon microscopy. One of the advantages of using multi-photon (or confocal) microscopy over epifluorescence imaging is z-stacking possibility and in consequence spatial co-localization of events occurring within extracellular matrix, e.g. tumor intravasation into lymphatic or blood vessel, which in the case of standard epifluorescence microscopy can be only inferred from morphological changes of the invading cell. This technique has far broader potential. For example, we have used the intravital IF to investigate the mechanism of lymphatic occlusion by lymphatic-specific photodynamic therapy27. Additional potential applications of this method include but are not limited to investigation of skin immunity during inflammation, mechanism of transplant rejection or methods of blood and lymphatic vessel growth during tumorigenesis.
Critical steps in the procedure
The most important step that has critical implications for sustaining a physiological tissue environment is a surgical separation of the ventral skin and cartilage from dorsal dermis. Cutting or occluding the major artery or vein will lead to excessive bleeding and local tissue hypoxia, which will affect cellular response to treatments and cell movement8. Immobilizing the ear with surgical glue should be done with care as spilling the glue on expose tissue will cause a permanent injury to the tissue by occlusion of blood vessels. The temperature of the mouse must be controlled and kept at 37 &#176;C. Additionally, humidified oxygen needs to be used for the isoflurane anesthesia, so that the eyes and lungs stay properly humidified during the experiment. Also, sodium ascorbate must be prepared freshly and its pH checked before use.
In summary, this intravital immunofluorescence bridges real-time, local measurements of physiological function with molecular imaging of complex cellular events in the mouse skin. Furthermore, this method has great potential as it can be easily applied to e.g. study post-developmental mechanisms of blood and lymph-angiogenesis or to visualize the early phases of skin infection by various pathogenic agents. With its flexibility and high-throughput potential, this intravital technique can significantly contribute to multiple fields of biology.

Intravital imaging of inflammatory, metastatic and matrix remodeling processes has been an important area of research and has motivated the creation of numerous transgenic reporter mouse models that express fluorescent proteins1,2. Due to out-of-focus fluorescent signals, which reduce image quality and limits light penetration through the tissue, imaging thick tissue is possible only with confocal or multi-photon scanning microscopy3. Using faster, less expensive and complex epifluorescence microscopy is possible only with nearly two-dimensional tissues such as the chicken chorio-allantoic membrane4 or mouse ear dermis5. Most imaging systems take advantage of transgenic mice expressing various fluorescent proteins in a cell type-specific fashion. Even though these proteins offer weak phototoxicity, they induce immune response6. Furthermore, it is difficult to switch between specific cell subtypes or mark their basal or activated states as such change requires the preparation of a new genetic model. In addition, as fluorescent protein expression is generally restricted to intracellular compartment, it is usually not possible to image extracellular structures like basement membrane proteins or tissue chemokine deposits7. Instead, indirect labeling with antibodies against extracellular antigens offers flexibility for virtually any cell-type or matrix specific component8,9. However, the major disadvantage of this labeling approach is associated with immunotoxicity mediated by antigen-antibody immune complexes that can trigger complement system-dependent cell toxicity and phagocytosis of cells and extracellular structures10.
The extracellular matrix of the tumor microenvironment, but also of normal tissue during inflammation or wound healing, undergoes substantial remodeling. Stromal stiffening of the tumor microenvironment can promote tumor growth and invasion due to stress-induced signaling mechanisms and cause remodeling of blood and lymphatic vessels11. However, live imaging of matrix proteins is limited to fibrillar collagens that can be detected by second harmonic generation using multi-photon microscopy. Recently we have published a novel intravital imaging method that minimizes the risk of photo- and immune-toxic damage to imaged cells and tissue structures5. In comparison with established imaging techniques where the single round of continuous intravital visualization is in a range of 30 minutes to 2 hours12-17, our intravital immunofluorescence (IF) technique allowed 12 hours (long-term 8) imaging. It is important to note that the imaging time is restricted to 12 hours due to limits defined in our animal protocol but there are no technical counter-indications that it cannot be prolonged if critical health parameters of the animal, like blood pressure and heart rate are controlled8. In addition, by using an automated fluorescence stereomicroscope we were able to collect images from multiple fields during a single experiment&#160;and observed rare immunological and remodeling processes that occurred in the physiological context of the skin supported by functional blood and lymphatic vessels. Because the stereomicroscopic lens has a relatively large, 2 cm, working distance and&#160;in contrast to two-photon microscopic optics&#160;does not require vaporizing water immersion, long-term imaging was performed only under fluorescence stereomicroscope. Intravital IF allowed the immune labeling and detection of any extracellular matrix component of the normal skin. The design of this technique is based on the innovative concept of using immunostaining for live cells and tissue matrix elements on surgically &#160;exposed mouse dermis without causing harmful immunotoxic effects5. The surgical procedure itself is safe to the dermis vasculature as it relies only on the separation of two skin layers in the ear that are independently innervated, autonomously fed by blood and drained by separate lymphatic circulations. Our experimental setup allows imaging of a range of important patho-physiological events over at least 12 hours, including leukocyte trafficking between blood and lymphatic vessels and wound healing processes. In the original publication, we compared our technique to state-of-the-art standards in various fields of intravital imaging. Consequently, we observed blood vessel extravasation and lymphatic intravasation events by various types of leukocytes, including the unique visualization of immune cells entering collecting instead of expected initial lymphatic vessels15. Also, complementing the observations done by other groups9,18, we found that in vivo CCL21 is able to form strong, discontinuous deposits on collecting but only infrequently on initial lymphatics.
Here we describe a modified intravital IF technique that can be combined with two-photon microscopy to detect network of fibrillar collagens using second harmonic generation (SHG). We show that this method can also be used for imaging cancer cell invasion in context of the dynamic tumor microenvironment, which includes matrix molecules such as tenascin C ,that are largely unexplored by current imaging techniques19. We found that the fibrillar matrix of the tumor, detected with the second harmonic generation, occupies different locations of the tumor microenvironment than the newly deposited matrix composed of tenascin C. Furthermore, we describe examples of vessel remodeling caused by local matrix contraction, long-term (12 hours) imaging of T-cell interactions with tumor cells and tumor cell migration along collagen IV of the basement membrane. Such events can be imaged while simultaneously recording local physiological parameters such as blood vessel permeability and lymphatic drainage.

<table border="0" cellpadding="0" cellspacing="0" width="966">
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			<td height="21" style="height:21px;width:515px;">Mice Strain</td>
			<td style="width:159px;"></td>
			<td style="width:119px;"></td>
			<td style="width:173px;"></td>
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			<td height="21" style="height:21px;width:515px;">BALB/C mice (8-12 weeks )</td>
			<td style="width:159px;">Charles River&#160;</td>
			<td style="width:119px;"></td>
			<td>Orleans,France</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;">C57/Bl6 Mice (8-12 weeks )</td>
			<td style="width:159px;">Harlan&#160;</td>
			<td style="width:119px;"></td>
			<td>Carshalton UK</td>
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			<td height="21" style="height:21px;width:515px;">Cell Line&#160;</td>
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			<td></td>
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			<td height="21" style="height:21px;width:515px;">B16 F10 Melanoma expressing OVA-GFP&#160;</td>
			<td style="width:159px;"></td>
			<td style="width:119px;"></td>
			<td></td>
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			<td height="21" style="height:21px;width:515px;">Anesthesia Maintenance&#160;</td>
			<td style="width:159px;"></td>
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			<td height="21" style="height:21px;width:515px;">Isofluorane&#160;</td>
			<td style="width:159px;">Minrad Inc.&#160;</td>
			<td align="right" style="width:119px;">2222</td>
			<td>Minrad Inc., Buffalo, NY</td>
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		<tr height="21">
			<td height="21" style="height:21px;">Humidified delivery system&#160;</td>
			<td style="width:159px;">Rothhacher GmBH&#160;</td>
			<td style="width:119px;"></td>
			<td>Berne, Switzerland&#160;</td>
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			<td height="21" style="height:21px;width:515px;">DC Temperature Control System&#160;</td>
			<td style="width:159px;">FHC Inc&#160;</td>
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			<td>Bowdoin, MA</td>
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			<td style="width:159px;"></td>
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			<td height="21" style="height:21px;width:515px;">Stereomicroscope&#160;</td>
			<td style="width:159px;"></td>
			<td style="width:119px;"></td>
			<td></td>
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		<tr height="63">
			<td height="63" style="height:63px;">Fluorescence stereomicroscope with a motorized stage .</td>
			<td style="width:159px;">M250 FA, Leica Microsystems CMS GmbH</td>
			<td style="width:119px;"></td>
			<td>Wetzlar, Germany</td>
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		<tr height="42">
			<td height="42" style="height:42px;width:515px;">&#160;1&#215; lens (linear system magnification from 7.5&#215; to 160&#215;)&#160;</td>
			<td style="width:159px;">Leica Microsystems CMS GmbH</td>
			<td style="width:119px;"></td>
			<td>Wetzlar, Germany</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:515px;">2&#215; lens (linear system magnification from 15.6&#215; to 320&#215;)</td>
			<td style="width:159px;">Leica Microsystems CMS GmbH</td>
			<td style="width:119px;"></td>
			<td>Wetzlar, Germany</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:515px;">DFC 350 FX camera controlled by LAS AF software&#160;</td>
			<td style="width:159px;">Leica Microsystems CMS GmbH</td>
			<td style="width:119px;"></td>
			<td>Wetzlar, Germany</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;"></td>
			<td style="width:159px;"></td>
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			<td height="21" style="height:21px;width:515px;">Multiphoton Microscopy&#160;</td>
			<td style="width:159px;"></td>
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			<td height="42" style="height:42px;">LEICA SP5, two-photon multiplier, motorized stage&#160;</td>
			<td style="width:159px;">Leica Microsystems CMS GmbH</td>
			<td style="width:119px;"></td>
			<td>Wetzlar, Germany</td>
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			<td height="21" style="height:21px;">HCX APO 20x/1.2 oil immersion&#160;</td>
			<td style="width:159px;"></td>
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			<td height="21" style="height:21px;">Chameleon Ultra Laser&#160;</td>
			<td style="width:159px;"></td>
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			<td height="21" style="height:21px;width:515px;">Reagents&#160;</td>
			<td style="width:159px;"></td>
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		<tr height="42">
			<td height="42" style="height:42px;width:515px;">Ringer&#39;s buffer (102 mM NaCl, 5 mM KCl, 2 mM CaCl2, 28 mM sodium lactate)</td>
			<td>B. Braun Medical AG</td>
			<td align="right">445968</td>
			<td>Sempach, Germany</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:515px;">Aprotinin&#160;</td>
			<td>Elastin</td>
			<td>AP92</td>
			<td>Owensville, MO</td>
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			<td height="21" style="height:21px;width:515px;">Thrombin&#160;</td>
			<td style="width:159px;">Sigma-Aldrich</td>
			<td>T7326-1KU&#160;</td>
			<td>Taufkirchen, Germany&#160;</td>
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			<td height="21" style="height:21px;">Sodium ascorbate</td>
			<td style="width:159px;">Sigma-Aldrich&#160;&#160;</td>
			<td>11140-50G&#160;</td>
			<td>Taufkirchen, Germany&#160;</td>
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			<td height="21" style="height:21px;width:515px;">Mouse Serum raised against human IgG&#160;</td>
			<td style="width:159px;">Abcam&#160;</td>
			<td>ab34834&#160;</td>
			<td>Cambridge, UK</td>
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			<td height="21" style="height:21px;width:515px;">Collagen IV&#160;</td>
			<td>Abcam</td>
			<td>AB6581</td>
			<td>Cambridge, UK</td>
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			<td height="21" style="height:21px;width:515px;">Perlacan&#160;</td>
			<td style="width:159px;">RnD&#160;</td>
			<td>ab79465&#160;</td>
			<td>Minneapolis, MN</td>
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			<td height="21" style="height:21px;width:515px;">Tenascin C&#160;</td>
			<td style="width:159px;">RnD&#160;</td>
			<td>AF3358</td>
			<td>Minneapolis, MN</td>
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			<td height="21" style="height:21px;width:515px;">Podoplanin</td>
			<td style="width:159px;">RnD&#160;</td>
			<td style="width:119px;">AF3244</td>
			<td>Minneapolis, MN</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;">LYVE-1&#160;</td>
			<td style="width:159px;">Reliatech&#160;</td>
			<td>103-PA50&#160;</td>
			<td>Wolfenb&#252;ttel, Germany</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;">CCL21</td>
			<td style="width:159px;">RnD</td>
			<td style="width:119px;">AF457</td>
			<td>Minneapolis, MN</td>
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			<td height="21" style="height:21px;width:515px;">Streptavidin Pacific Blue&#160;</td>
			<td style="width:159px;">Invitrogen&#160;</td>
			<td>S11222</td>
			<td>Grand Island, NY</td>
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			<td height="21" style="height:21px;width:515px;">Streptavidin Alexa 647&#160;</td>
			<td style="width:159px;">Invitrogen&#160;</td>
			<td>S21374</td>
			<td>Grand Island, NY</td>
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			<td height="21" style="height:21px;width:515px;">Streptavidin Alexa 488&#160;</td>
			<td style="width:159px;">Invitrogen&#160;</td>
			<td style="width:119px;">S11223</td>
			<td>Grand Island, NY</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;">Donkey Anti Goat 594&#160;</td>
			<td style="width:159px;">Invitrogen&#160;</td>
			<td>A21113</td>
			<td>Grand Island, NY</td>
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			<td height="21" style="height:21px;width:515px;">Donkey Anti Rabbit 594&#160;</td>
			<td style="width:159px;">Invitrogen&#160;</td>
			<td>A21207</td>
			<td>Grand Island, NY</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:515px;">CMTPX CellTracker</td>
			<td style="width:159px;">Lifetechnologies</td>
			<td style="width:119px;">C34552</td>
			<td>Carlsbad, California</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:515px;">Histocryl (surgical glue)</td>
			<td style="width:159px;">Braun Aesculap</td>
			<td style="width:119px;">1050060</td>
			<td>Tuttlingen, Germany</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:515px;"></td>
			<td style="width:159px;"></td>
			<td style="width:119px;"></td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:515px;">Cell Culture Reagents&#160;</td>
			<td style="width:159px;"></td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dulbecco&#8217;s modified Eagle&#8217;s medium (DMEM</td>
			<td>Gibco Invitrogen</td>
			<td>E15-843&#160;</td>
			<td>Grand Island, NY</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Fetal bovine serum (FBS</td>
			<td>Gibco Invitrogen</td>
			<td style="width:119px;"></td>
			<td>Grand Island, NY</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trypsin</td>
			<td>Gibco Invitrogen</td>
			<td>25300062</td>
			<td>Grand Island, NY</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:515px;">PBS&#160;</td>
			<td>Gibco Invitrogen</td>
			<td style="width:119px;"></td>
			<td>Grand Island, NY</td>
		</tr>
	</tbody>
</table>

long-term intravital immunofluorescence imaging of tissue matrix components with epifluorescence and two-photon microscopy

Besides being a physical scaffold to maintain tissue morphology, the extracellular matrix (ECM) is actively involved in regulating cell and tissue function during development and organ homeostasis. It does so by acting via biochemical, biomechanical, and biophysical signaling pathways, such as through the release of bioactive ECM protein fragments, regulating tissue tension, and providing pathways for cell migration. The extracellular matrix of the tumor microenvironment undergoes substantial remodeling, characterized by the degradation, deposition and organization of fibrillar and non-fibrillar matrix proteins. Stromal stiffening of the tumor microenvironment can promote tumor growth and invasion, and cause remodeling of blood and lymphatic vessels. Live imaging of matrix proteins, however, to this point is limited to fibrillar collagens that can be detected by second harmonic generation using multi-photon microscopy, leaving the majority of matrix components largely invisible. Here we describe procedures for tumor inoculation in the thin dorsal ear skin, immunolabeling of extracellular matrix proteins and intravital imaging of the exposed tissue in live mice using epifluorescence and two-photon microscopy. Our intravital imaging method allows for the direct detection of both fibrillar and non-fibrillar matrix proteins in the context of a growing dermal tumor. We show examples of vessel remodeling caused by local matrix contraction. We also found that fibrillar matrix of the tumor detected with the second harmonic generation is spatially distinct from newly deposited matrix components such as tenascin C. We also showed long-term (12 hours) imaging of T-cell interaction with tumor cells and tumor cells migration along the collagen IV of basement membrane. Taken together, this method uniquely allows for the simultaneous detection of tumor cells, their physical microenvironment and the endogenous tissue immune response over time, which may provide important insights into the mechanisms underlying tumor progression and ultimate success or resistance to therapy.

To date, immunostaining in live tissue is not typically used due to formation of immune complexes leading to high staining background and immunotoxicity20. This was overcome by pre-blocking Fc&#947; receptors on tissue macrophages, thus "blinding" these cells to subsequent indirect strong immunostaining. As the labeling was extracellular, phototoxicity and fluorophore bleaching could be controlled by immersion of the tissue in natural antioxidant buffered, isosmotic ascorbic acid (Fig. 1A). Since our initial description of this method5, we improved our anti-bleaching and anti-phototoxic technique so that photobleaching can now not only be inhibited but completely prevented (Fig. 1B). This is done by embedding the ear in a large volume of antioxidant (100 &#956;l) within the chamber where the ear is immobilized. Note that 300 seconds constant imaging time corresponds to 10 hours of imaging when pictures are collected for 500 msec every one minute (the average imaging settings).
<img alt="Figure 1" fo:content-width="5in" fo:src="/files/ftp_upload/51388/51388fig1highres.jpg" src="/files/ftp_upload/51388/51388fig1.jpg" /> 
Figure 1. Photobleaching and phototoxicity was stopped by replacing chloride with ascorbate in Ringer's buffer and embedding the exposed ear in 100 &#956;l volume of that solution. (A) Tissue was stained first with a biotinylated antibody against collagen IV, the component of the basement membrane. The staining was later detected with streptavidin-647 (red), and then constantly imaged for 300 seconds in either normal Ringer's buffer (upper panel) or ascorbate-Ringer's (lower panel). Note that 300 seconds constant imaging time corresponds to 10 hours of imaging when pictures are collected for 500 msec every one minute (the usual imaging settings). The brightest 25% of pixel intensity values are green colored. (B) Quantification of immunofluorescence decay (50% in Ringer's vs. 0% in ascorbate-Ringer's). Values were normalized to the initial fluorescence. Images collected with immunofluorescence stereomicroscope. Scale bar in A, 100 &#181;m. <a href="https://www.jove.com/files/ftp_upload/51388/51388fig1highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Investigating the interaction between tumor metastatic cells and tumor stroma is crucial to understand the process of tumor cell migration and tumor immunity. This is because the tumor-associated stroma composes up to 90% of the tumor mass and actively regulates tumor growth and metastatic spread21. However, mechanistic insight into how the matrix drives tumor cell migration towards either lymphatic or blood vessels is lacking 22. This is partially due to the fact that intravital imaging of matrix proteins is limited to the visualization of matured fibers of fibrillar collagens using second harmonic generation in two-photon microscopy23. Therefore, we adapted our method for the visualization of the tissue microenvironment including blood and lymphatic vessels, pericytes, nerves, muscle and adipocytes to include the direct visualization of extracellular matrix components. Many structures can be distinguished based on their morphology after immunostaining for basement membrane components such as collagen IV or perlecan (Fig. 2A), however, direct staining for specific cell surface markers, e.g. Lyve1 (Fig. 2B and C) and podoplanin (Fig. 2C), further allows distinguishing initial, capillary lymphatics (Lyve1+) from lymphatic collectors (Lyve1-). Staining for matrix-bound CCL21 in the skin revealed deposits of this chemokine on the basement membrane of lymphatic collectors identified with the staining for perlecan, the heparan sulphate proteoglycan (Fig. 2D).
<img alt="Figure 2" fo:content-width="5in" fo:src="/files/ftp_upload/51388/51388fig2highres.jpg" src="/files/ftp_upload/51388/51388fig2.jpg" /> 
Figure 2. Examples of live staining in a normal mouse ears. (A) Staining for perlecan, a basement membrane component, depicts all blood and lymphatic vessels, nerves, muscle fibers and adipocytes. (B) Lyve1 staining marks the initial lymphatic capillary network. (C) Co-staining for Lyve1 and podoplanin, a pan-lymphatic marker, depicts networks of initial and collecting lymphatics. The dorsal ear dermis can be imaged using classic epifluorescence microscopy (without optical sectioning) as the ear dermis has low number of adipocytes that would otherwise cover the imaging field. (D) CCL21 staining (green) on lymphatic basement membrane stained for perlecan (red). Images collected with immunofluorescence stereomicroscope. Scale bars in A and B, 1 mm; in C, 100 &#956;m and 50 &#956;m in D. <a href="https://www.jove.com/files/ftp_upload/51388/51388fig2highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Most importantly, structural proteins that normally cannot be detected by SHG, the classic matrix detection method23, can be visualized. For example, we found that tenascin C (Fig. 3A), a matrix protein that is expressed during tumorigenesis, wound healing and inflammation19 is deposited in different locations of tumor stroma than fibrillar collagens (Fig. 3B). This matrix heterogeneity might affect tumor cell distribution and metastasis (Fig. 3C).
<img alt="Figure 3" fo:content-width="5in" fo:src="/files/ftp_upload/51388/51388fig3highres.jpg" src="/files/ftp_upload/51388/51388fig3.jpg" /> 
Figure 3. The dorsal ear dermis can be live imaged using multi-photon microscopy. A single field of tumor B16-F10. Tumor stroma was labeled with tenascin C antibody and the staining was detected with anti-goat-594 donkey antibody. Immunofluorescence of tenascin C (red) network is shown in A and fibrillar collagens detected with second harmonic generation (SGH) in B. These two networks are superimposed with tumor cells (cyan) in C (merged). New tumor matrix marked by tenascin C is not overlapping with fibrillar collagens detected with SHG (green). The image with 44, four times averaged z-sections with z-step 1.0 &#956;m was acquired in 16 bit color depth mode. Images collected with two-photon microscope. Scale bar, 100 &#956;m. <a href="https://www.jove.com/files/ftp_upload/51388/51388fig3highres.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Following the immunolabeling of different tumor matrix components (e.g. tenascin C and collagen IV) of tumor matrix we could identified restricted and sudden events of tumor matrix directional remodeling (Video 1). Forces that develop within tumor microenvironment may lead to expansion or contraction of the tumor matrix and in consequence remodeling and elongation of the tumor vasculature to a similar extent as we showed previously in the case of healing wounds11,24.
Video 1. Expansion of tumor matrix labeled with collagen IV (red) and tenascin C (cyan) elongate blood vessels (arrow) and passively translocate three tumor cells (green). Localized contraction of teascin C-rich tumor matrix translocate blood vessel (red horizontally oriented structure) by approximately 100 &#956;m during 12 hours of imaging. Images collected with immunofluorescence stereomicroscope. <a href="https://www.jove.com/files/ftp_upload/51388/Video1_New.avi" target="_blank">Click here to view video.</a>
Using multi-photon microscopy with fluorophore labeling is problematic as photon flux used in these experiments will quickly bleach fluorescent dyes that are not protected from oxidation25. Here we show that we can perform two-photon time-lapse microscopy while simultaneously imaging immunolabeled tenascin C matrix with minimal photobleaching of fluorophores even in high photon density two-photon microscopy (Video 2).
Video 2. Low level photobleaching of tenascin C immunofluorescence (red) during two-photon microscopy. B16-F10-GFP tumor cells (cyan) were imaged in the open dorsal ear 9 days after inoculation. The fluorescent signal was protected by application of ascorbate-Ringer's buffer onto the imaged tissue. Second harmonic generation (green) is not overlapping with new matrix represented by tenascin C. 16 bit color depth image with 11, four times averaged z-sections with z-step 1.9 &#956;m was acquired for 15 min. Images were collected every 1 minute 5 seconds in 6 z-planes collected. <a href="https://www.jove.com/files/ftp_upload/51388/Video2.avi" target="_blank">Click here to view video.</a>
We also imaged immune-cell interactions with metastatic tumor cells. CMTPX-labeled splenocytes from a tumor-bearing mouse extravasated from tumor-associated blood vessels 8 hours after i.v. transfusion, invaded the tumor matrix and actively interacted with tumor cells by forming long-lasting cell contacts (Video 2). Fluorophore-647-labeled collagen IV structures were resistant to photobleaching during the 12 hours of imaging.
Video 3. Interaction of CMTPX-labeled splenocytes from tumor (B16-F10)-bearing mouse with individual tumor cells (GFP- B16-F10). Splenocytes were i.v. transfused after tissue staining for collagen IV. Collagen IV-green (647), splenocytes-red (CMTPX), B16-F10 cyan (GFP). Images collected with immunofluorescence stereomicroscope. Video duration 12 hours. <a href="https://www.jove.com/files/ftp_upload/51388/Video3-corrected.mov" target="_blank">Click here to view video.</a>
Freshly isolated tumor cells were overlaid on the exposed ear dermis pre-stained for collagen IV. We could observed that after adhering to the tissue some groups of cells started collective migration along basement membrane of blood vessels and adipocytes.
Video 4. Tumor cells migrate along basement membranes. Normal ear skin stained for collagen IV (647, red) was overlaid with freshly passaged B16-F10-GFP cells and imaged for 5 hours. Some tumor cells that adhered to tissue started collective migration along basement membrane of blood vessels and adipocytes. Images collected with immunofluorescence stereomicroscope. Video duration: 5 hours. <a href="https://www.jove.com/files/ftp_upload/51388/Video4.avi" target="_blank">Click here to view video.</a>
Also, because the ear dermis is virtually two-dimensional, we could readily collect large volumes of data using fast fluorescence stereomicroscopy, instead of slower and more expensive confocal or multiphoton microscopy. However, it is also possible to use any of the mentioned scanning microscopy methods with our intravital IF preparations (Fig. 3, Video 1).

Watch this Scientific Journal Video about Long-term Intravital Immunofluorescence Imaging of Tissue Matrix Components with Epifluorescence and Two-photon Microscopy at JoVE.com

Long-term Intravital Immunofluorescence Imaging of Tissue Matrix Components with Epifluorescence and Two-photon Microscopy

The extracellular matrix undergoes substantial remodeling during wound healing, inflammation and tumorigenesis. We present a novel intravital immunofluorescence microscopy approach to visualize the dynamics of fibrillar as well as mesh-like matrix components with high spatial and temporal resolution using epifluorescence or two-photon microscopy.

Besides being a physical scaffold to maintain tissue morphology, the extracellular matrix (ECM) is actively involved in regulating cell and tissue ...

long-term-intravital-immunofluorescence-imaging-tissue-matrix

Research

JoVE Journal

Bioengineering

19.0K vues.  École Polytechnique Fédérale de Lausanne.  La matrice extracellulaire subit un remodelage important lors de la cicatrisation des plaies, l'inflammation et la tumorigenèse. Nous présentons une nouvelle approche de microscopie par immunofluorescence intravitale de visualiser la dynamique des fibrillaire ainsi que maille-comme composants de la matrice avec une résolution spatiale et temporelle en utilisant épifluorescence ou la microscopie à deux photons. 

Vidéo: Long-term Intravital Immunofluorescence Imaging of Tissue Matrix Components with Epifluorescence and Two-photon Microscopy

Non-contact, Label-free Monitoring of Cells and Extracellular Matrix using Raman Spectroscopy

Non-destructive, non-contact and label-free technologies to monitor cell and tissue cultures are needed in the field of biomedical research.1-5 However, currently available routine methods require processing steps and alter sample integrity. Raman spectroscopy is a fast method that enables the measurement of biological samples without the need for further processing steps. This laser-based technology detects the inelastic scattering of monochromatic light.6 As every chemical vibration is assigned to a specific Raman band (wavenumber in cm-1), each biological sample features a typical spectral pattern due to their inherent biochemical composition.7-9 Within Raman spectra, the peak intensities correlate with the amount of the present molecular bonds.1 Similarities and differences of the spectral data sets can be detected by employing a multivariate analysis (e.g. principal component analysis (PCA)).10
Here, we perform Raman spectroscopy of living cells and native tissues. Cells are either seeded on glass bottom dishes or kept in suspension under normal cell culture conditions (37 &deg;C, 5% CO2) before measurement. Native tissues are dissected and stored in phosphate buffered saline (PBS) at 4 &deg;C prior measurements. Depending on our experimental set up, we then either focused on the cell nucleus or extracellular matrix (ECM) proteins such as elastin and collagen. For all studies, a minimum of 30 cells or 30 random points of interest within the ECM are measured. Data processing steps included background subtraction and normalization.

Raman spectroscopy is a suitable technique for the non-contact, label-free analysis of living cells, tissue-engineered constructs and native tissues. Source-specific spectral fingerprints can be generated and analyzed using multivariate analysis.

Non-destructive, non-contact and label-free technologies to monitor cell and tissue cultures are needed in the field of biomedical research.1-5 However, ...

The Multi-organ Chip - A Microfluidic Platform for Long-term Multi-tissue Coculture

The ever growing amount of new substances released onto the market and the limited predictability of current in vitro test systems has led to a high need for new solutions for substance testing. Many drugs that have been removed from the market due to drug-induced liver injury released their toxic potential only after several doses of chronic testing in humans. However, a controlled microenvironment is pivotal for long-term multiple dosing experiments,&#160;as even minor alterations in extracellular conditions may greatly influence the cell physiology. We focused within our research program on the generation of a microengineered bioreactor, which can be dynamically perfused by an on-chip pump and combines at least two culture spaces for multi-organ applications. This circulatory system mimics the in vivo conditions of primary cell cultures better and assures a steadier,&#160;more quantifiable extracellular relay of signals to the cells. 
For demonstration purposes, human liver equivalents, generated by aggregating differentiated HepaRG cells with human hepatic stellate cells in hanging drop plates, were cocultured with human skin punch biopsies for up to 28 days inside the microbioreactor. The use of cell culture inserts enables the skin to be cultured at an air-liquid interface, allowing topical substance exposure. The microbioreactor system is capable of supporting these cocultures at near physiologic fluid flow and volume-to-liquid ratios, ensuring stable and organotypic culture conditions. The possibility of long-term cultures enables the repeated exposure to substances. Furthermore, a vascularization of the microfluidic channel circuit using human dermal microvascular endothelial cells yields a physiologically more relevant vascular model.

Here, we present a protocol to coculture primary cells, tissue models and punch biopsies in a microfluidic multi-organ chip for up to 28 days. Human dermal microvascular endothelial cells, liver aggregates and skin biopsies were successfully combined in a common media circulation.

The ever growing amount of new substances released onto the market and the limited predictability of current in vitro test systems has led to a high need ...

Long-term Live Imaging Device for Improved Experimental Manipulation of Zebrafish Larvae

The zebrafish larva is an important model organism for both developmental biology and wound healing. Further, the zebrafish larva is a valuable system for live high-resolution microscopic imaging of dynamic biological phenomena in space and time with cellular resolution. However, the traditional method of agarose encapsulation for live imaging can impede larval development and tissue regrowth. Therefore, this manuscript describes the zWEDGI (zebrafish Wounding and Entrapment Device for Growth and Imaging), which was designed and fabricated as a functionally compartmentalized device to orient larvae for high-resolution microscopy while permitting caudal fin transection within the device and subsequent unrestrained tail development and re-growth. This device allows for wounding and long-term imaging while maintaining viability. Given that the zWEDGI mold is 3D printed, the customizability of its geometries make it easily modified for diverse zebrafish imaging applications. Furthermore, the zWEDGI offers numerous benefits, such as access to the larva during experimentation for wounding or for the application of reagents, paralleled orientation of multiple larvae for streamlined imaging, and reusability of the device.

This manuscript describes the zWEDGI (zebrafish Wounding and Entrapment Device for Growth and Imaging), which is a compartmentalized device designed to orient and restrain zebrafish larvae. The design permits tail transection and long-term collection of high-resolution fluorescent microscopy images of wound healing and regeneration.

The zebrafish larva is an important model organism for both developmental biology and wound healing. Further, the zebrafish larva is a valuable system for ...

A Novel Tenorrhaphy Suture Technique with Tissue Engineered Collagen Graft to Repair Large Tendon Defects

Surgical management of large tendon defects with tendon grafts is challenging, as there are a finite number of sites where donors can be readily identified and used. Currently, this gap is filled with tendon auto-, allo-, xeno-, or artificial grafts, but clinical methods to secure them are not necessarily translatable to animals because of the scale. In order to evaluate new biomaterials or study a tendon graft made up of collagen type 1, we have developed a modified suture technique to help maintain the engineered tendon in alignment with the tendon ends. Mechanical properties of these grafts are inferior to the native tendon. To incorporate engineered tendon into clinically relevant models of loaded repair, a strategy was adopted to offload the tissue engineered tendon graft and allow for the maturation and integration of the engineered tendon in vivo until a mechanically sound neo-tendon was formed. We describe this technique using incorporation of the collagen type 1 tissue engineered tendon construct.

In this paper, we present an in vitro and in situ protocol to repair a tendon gap of up to 1.5 cm by filling it with engineered collagen graft. This was performed by developing a modified suture technique to take the mechanical load until the graft matures into the host tissue.

Surgical management of large tendon defects with tendon grafts is challenging, as there are a finite number of sites where donors can be readily ...

Visualizing Adhesion Formation in Cells by Means of Advanced Spinning Disk-Total Internal Reflection Fluorescence Microscopy

In living cells, processes such as adhesion formation involve extensive structural changes in the plasma membrane and the cell interior. In order to visualize these highly dynamic events, two complementary light microscopy techniques that allow fast imaging of live samples were combined: spinning disk microscopy (SD) for fast and high-resolution volume recording and total internal reflection fluorescence (TIRF) microscopy for precise localization and visualization of the plasma membrane. A comprehensive and complete imaging protocol will be shown for guiding through sample preparation, microscope calibration, image formation and acquisition, resulting in multi-color SD-TIRF live imaging series with high spatio-temporal resolution. All necessary image post-processing steps to generate multi-dimensional live imaging datasets, i.e. registration and combination of the individual channels, are provided in a self-written macro for the open source software ImageJ. The imaging of fluorescent proteins during initiation and maturation of adhesion complexes, as well as the formation of the actin cytoskeletal network, was used as a proof of principle for this novel approach. The combination of high resolution 3D microscopy and TIRF provided a detailed description of these complex processes within the cellular environment and, at the same time, precise localization of the membrane-associated molecules detected with a high signal-to-background ratio.

An advanced microscope that permit fast and high-resolution imaging of both, the isolated plasma membrane and the surrounding intracellular volume, will be presented. The integration of spinning disk and total internal reflection fluorescence microscopy in one setup allows live imaging experiments at high acquisition rates up to 3.5 s per image stack.

In living cells, processes such as adhesion formation involve extensive structural changes in the plasma membrane and the cell interior. In order to ...

Pancreatic Tissue-Derived Extracellular Matrix Bioink for Printing 3D Cell-Laden Pancreatic Tissue Constructs

The transplantation of pancreatic islets is a promising treatment for patients who suffer from type 1 diabetes accompanied by hypoglycemia and secondary complications. However, islet transplantation still has several limitations such as the low viability of transplanted islets due to poor islet engraftment and hostile environments. In addition, the insulin-producing cells differentiated from human pluripotent stem cells have limited ability to secrete sufficient hormones that can regulate the blood glucose level; therefore, improving the maturation by culturing cells with proper microenvironmental cues is strongly required. In this article, we elucidate protocols for preparing a pancreatic tissue-derived decellularized extracellular matrix (pdECM) bioink to provide a beneficial microenvironment that can increase glucose sensitivity of pancreatic islets, followed by describing the processes for generating 3D pancreatic tissue constructs using a microextrusion-based bioprinting technique.

Decellularized extracellular matrix (dECM) can provide suitable microenvironmental cues to recapitulate the inherent functions of target tissues in an engineered construct. This article elucidates the protocols for the decellularization of pancreatic tissue, evaluation of pancreatic tissue-derived dECM bioink, and generation of 3D pancreatic tissue constructs using a bioprinting technique.

The transplantation of pancreatic islets is a promising treatment for patients who suffer from type 1 diabetes accompanied by hypoglycemia and secondary ...

Targeting the Rat's Small Bowel: Long-Term Infusion into the Superior Mesenteric Artery

The superior mesenteric artery can be cannulated in humans through minimally invasive radiological catheterization of the femoral or axillary artery. SMA cannulation is more difficult in rats due to small anatomical dimensions. The aim of the study is to describe a surgical technique for cannulation of the SMA in rats to perform long-term infusion of drugs into the SMA vascular bed in unrestricted animals, which will result in a high rate of catheter patency after the post surgical recovery for 24 hours. 
To avoid the risk of SMA thrombosis or bleeding from direct access, a proximal branch of the SMA is isolated, ligated distally and cannulated with a 0.25 mm polyurethane capillary tube whose tip is advanced close to the origin of the SMA from the aorta. The cannula is then tunnelled subcutaneously to the back of the animal's neck and through the skin via an artificial valve. The external portion of the cannula is inserted in a semi-rigid support system and connected to the continuous infusion pump outside the cage where the rat is free to move. 
Correct positioning of the cannula was demonstrated by post-surgical angiography and autopsy findings. Catheter patency after 24 hours of saline infusion into the SMA region was assured in most rats by the total discharge of the pump and recognition of a functional cannula for blood sampling or saline infusion.

Targeting the Rat&#039;s Small Bowel: Long-Term Infusion into the Superior Mesenteric Artery

Access for long-term infusion in the superior mesenteric artery (SMA) of rats is a surgical procedure that consists of cannulation of a proximal branch of the SMA. The cannula exits from the abdominal wound and is tunneled through the subcutaneous space back to the interscapular fold.

The superior mesenteric artery can be cannulated in humans through minimally invasive radiological catheterization of the femoral or axillary artery. SMA ...

A Simple Microfluidic Chip for Long-Term Growth and Imaging of Caenorhabditis elegans

Caenorhabditis elegans (C. elegans) have proved to be a valuable model system for studying developmental and cell biological processes. Understanding these biological processes often requires long-term and repeated imaging of the same animal. Long recovery times associated with conventional immobilization methods done on agar pads have detrimental effects on animal health making it inappropriate to repeatedly image the same animal over long periods of time. This paper describes a microfluidic chip design, fabrication method, on-chip C. elegans culturing protocol, and three examples of long-term imaging to study developmental processes in individual animals. The chip, fabricated with polydimethylsiloxane and bonded on a cover glass, immobilizes animals on a glass substrate using an elastomeric membrane that is deflected using nitrogen gas. Complete immobilization of C. elegans enables robust time-lapse imaging of cellular and sub-cellular events in an anesthetic-free manner. A channel geometry with a large cross-section allows the animal to move freely within two partially sealed isolation membranes permitting growth in the channel with a continuous food supply. Using this simple chip, imaging of developmental phenomena such as neuronal process growth, vulval development, and dendritic arborization in the PVD sensory neurons, as the animal grows inside the channel, can be performed. The long-term growth and imaging chip operates with a single pressure line, no external valves, inexpensive fluidic consumables, and utilizes standard worm handling protocols that can easily be adapted by other laboratories using C. elegans.

A Simple Microfluidic Chip for Long-Term Growth and Imaging of Caenorhabditis elegans

The protocol describes a simple microfluidic chip design and microfabrication methodology used to grow C. elegans in presence of a continuous food supply for up to 36 h. The growth and imaging device also enables intermittent long-term high-resolution imaging of cellular and sub-cellular processes during development for several days.

Caenorhabditis elegans (C. elegans) have proved to be a valuable model system for studying developmental and cell biological processes. Understanding ...

In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy

Stimulated Raman scattering (SRS) microscopy enables label-free imaging of the biological tissues in its natural microenvironment based on intrinsic molecular vibration, thus providing a perfect tool for in vivo study of biological processes at subcellular resolution. By integrating two-photon excited fluorescence (TPEF) imaging into the SRS microscope, the dual-modal in vivo imaging of tissues can acquire critical biochemical and biophysical information from multiple perspectives which helps understand the dynamic processes involved in cellular metabolism, immune response and tissue remodeling, etc. In this video protocol, the setup of a TPEF-SRS microscope system as well as the in vivo imaging method of the animal spinal cord is introduced. The spinal cord, as part of the central nervous system, plays a critical role in the communication between the brain and peripheral nervous system. Myelin sheath, abundant in phospholipids, surrounds and insulates the axon to permit saltatory conduction of action potentials. In vivo imaging of myelin sheaths in the spinal cord is important to study the progression of neurodegenerative diseases and spinal cord injury. The protocol also describes animal preparation and in vivo TPEF-SRS imaging methods to acquire high-resolution biological images.

In vivo Imaging of Biological Tissues with Combined Two-Photon Fluorescence and Stimulated Raman Scattering Microscopy

Stimulated Raman scattering (SRS) microscopy allows label-free imaging of biomolecules based on their intrinsic vibration of specific chemical bonds. In this protocol, the instrumental setup of an integrated SRS and two-photon fluorescence microscope is described to visualize cellular structures in the spinal cord of live mice.

Stimulated Raman scattering (SRS) microscopy enables label-free imaging of the biological tissues in its natural microenvironment based on intrinsic ...

Highly-Multiplexed Tissue Imaging with Raman Dyes

Visualizing a vast scope of specific biomarkers in tissues plays a vital role in exploring the intricate organizations of complex biological systems. Hence, highly multiplexed imaging technologies have been increasingly appreciated. Here, we describe an emerging platform of highly-multiplexed vibrational imaging of specific proteins with comparable sensitivity to standard immunofluorescence via electronic pre-resonance stimulated Raman scattering (epr-SRS) imaging of rainbow-like Raman dyes. This method circumvents the limit of spectrally-resolvable channels in conventional immunofluorescence and provides a one-shot optical approach to interrogate multiple markers in tissues with subcellular resolution. It is generally compatible with standard tissue preparations, including paraformaldehyde-fixed tissues, frozen tissues, and formalin-fixed paraffin-embedded (FFPE) human tissues. We envisage this platform will provide a more comprehensive picture of protein interactions of biological specimens, particularly for thick intact tissues. This protocol provides the workflow from antibody preparation to tissue sample staining, to SRS microscope assembly, to epr-SRS tissue imaging.

Electronic pre-resonance stimulated Raman scattering (epr-SRS) imaging of rainbow-like Raman dyes is a new platform for highly multiplexed epitope-based protein imaging. Here, we present a practical guide including antibody preparation, tissue sample staining, SRS microscope assembly, and epr-SRS tissue imaging.

Visualizing a vast scope of specific biomarkers in tissues plays a vital role in exploring the intricate organizations of complex biological systems. ...