The authors thank their funding sources, Howard Hughes Medical Institute Undergraduate Science Education Program to the College of William and Mary; Grant sponsor: NIH (M.S.S); Grant number: R15NS067566. They also acknowledge support from the College of William and Mary, Department of Biology and College of Arts and Sciences for assistance with animal care.

Ethics Statement: The methods were conducted with domesticated zebra finches from the breeding colony at the College of William and Mary. All procedures followed RSPCA guidelines23 and were approved by the College of William and Mary&#8217;s OLAW (Office of Laboratory Animal Welfare) Animal Welfare Assurance (#A3713-01) and had Institutional Animal Care and Use Committee (IACUC) approval (#2013-06-02-8721-dacris).
1. Egg Collection and Incubation
<ol>
	<li>Establish zebra finch pairs on a 14:10 light: dark cycle. Supply food, water, hay, and a nest box ad libitum. Note: Routine care and breeding for zebra finches has been well described23.</li>
	<li>Prepare a standard chick incubator with tilting shelves. Note: Maintain the artificial incubator at 37.5 (+/- 1) &#176;C with 80 - 95% humidity by adding water to the bottom of the incubator on a daily basis. Allow the incubator to equilibrate for two days before using.
	<ol>
		<li>Select small feed cups (5 x 7.6 cm) at least 2.5 cm deep to hold eggs in the incubator. Line the bottom and lower edges of the cup with two layers of paper towel so that the cup is padded, while still allowing the eggs to easily roll. Place these cups on the tilting shelves of the incubator. Note: Too much padding can inhibit rolling, which will prevent successful incubation due to embryonic adhesion to the shell interior.</li>
	</ol>
	</li>
	<li>Collect the eggs at two hours following the onset of the light cycle. Note: This minimizes discrepancies in stage development for a given incubation time due to parental incubation.
	<ol>
		<li>Pick up eggs gently with thumb and forefinger at the tip and base along the length of the egg. Use a dull, soft 4B graphite pencil to label the date laid and time collected from the nest. Note: The softer 4B pencil reduces the risk of the pencil breaking the fragile eggshell.</li>
		<li>1.3.2) Place 1 - 5 labeled eggs in each cup in the incubator so that eggs can freely roll to prevent embryonic adhesion to the interior of the shell. Note: Placing more than 5 eggs in a cup may prevent rolling of the individual eggs and reduce viability of embryos.</li>
	</ol>
	</li>
</ol>
2. Removal of Embryo from Egg
<ol>
	<li>To prepare for dissection, assemble the following materials: a clean scalpel, fine tipped forceps, and two extra fine tipped forceps. Place 10 x 10 cm weigh paper on the base of the dissecting scope to provide a clean, non-absorbent surface for dissection. Note: The weigh paper is crucial because it allows easy manipulation of the yolk and is the best surface for cutting the delicate membranes with a scalpel.</li>
	<li>Prepare an aliquot of phosphate buffer saline (1X PBS) in a 50 ml polypropylene tube, and acquire at least three transfer pipettes and a small waste bucket. If fixing the embryos, prepare an aliquot of 4% paraformaldehyde (PFA).Caution: PFA vapors are toxic, and all steps involving PFA should be done inside a fume hood to minimize exposure. If flash freezing the embryos, obtain liquid nitrogen and keep it near the dissecting scope. Sterility is not an issue for this dissection protocol, but ensure all materials are clean.</li>
	<li>Remove the egg from the incubator at the time point needed for the desired stage as described in the zebra finch staging guide22. Note: Remove eggs after 36 hr of incubation to dissect stage 6 embryos (Figure&#160;4A)22 and remove eggs after 56 hr of incubation to dissect stage 12 embryos (Figure&#160;3A)22.</li>
	<li>Using a fiber optic illuminator lamp, candle the egg by holding it along its vertical axis and shine light through the egg to illuminate the interior. Place the tip of the light behind the egg and locate the yolk and the developing embryo.
	<ol>
		<li>Position the scalpel on the side opposite the yolk and cut along the egg from tip to base with faint pressure.</li>
	</ol>
	</li>
	<li>Remove the contents of the egg by carefully applying pressure on the tip and base of the egg with the thumb and the forefinger, or by gently prying apart the eggshell along the cut with forceps. Open the egg directly above the weigh paper so that the yolk gently rolls out.</li>
	<li>Examine the yolk for the white zone of junction, which is visible as a faint white ring encircling embryonic development and orient the yolk using extra fine tipped forceps so that the embryo is located in the center. 
	Note: If a faint white circle on the surface of the yolk is not observed, take the fine forceps and gently roll the yolk over until the embryo is on top of the yolk. Note: For stages 1 - 922, the embryonic disk is less than 6 mm in diameter and is visible as a faint, slightly opaque disk on the surface of the yolk - see Figure 1 for reference. For stages 10 and older22, blood pools allow improved visibility of the embryo, but take care to avoid puncturing the yolk sac, as this makes locating the embryo difficult.</li>
</ol>
3. Separation of Embryo from Extra-embryonic Tissue
<ol>
	<li>Puncture the edges of the yolk to relieve pressure (Figure 1B), and make single cuts across the length of the yolk diameter alongside the embryonic disk. Repeat making these diagonal lines until the section of the yolk containing the embryo has been successfully separated (Figure 1B). Note: This step allows the yolk mass to remain intact, but the reduced pressure on the surface of the yolk allows for more precision when cutting around the embryo, preventing damage to embryonic structures.</li>
	<li>Remove the edges of the yolk with a transfer pipette. Note: Remove as much yolk as possible, but leave a small amount so that the embryo does not adhere to the dry surface of the weigh paper and tear.</li>
	<li>Wash the embryonic disk by dispensing 1X PBS at a 45&#176; angle towards the bottom of the embryo. Place the tip of the transfer pipette next to&#8212;not above&#8212;the embryonic disk. If additional yolk needs to be removed, separate any yolk with the scalpel on the weigh paper before transferring the embryo to the Petri dish. Note: This method removes the embryo from the surface of the weigh paper.</li>
	<li>Transfer the embryo using a transfer pipette along with a minimal volume of 1X PBS to a small, plastic Petri dish. Wash the embryo by adding more 1X PBS into the Petri dish and dripping 1X PBS near, but not directly onto, the embryo. Swirl the Petri dish to wash and remove residual yolk, tilt the Petri dish, and remove waste 1X PBS with the transfer pipette. 
	NOTE: When the 1X PBS is removed, the embryo typically does not adhere to the bottom of the Petri dish because the plastic surface is slippery with residual 1X PBS. However, more 1X PBS can be added if the embryo sticks to the dish. 
	If fixing the embryo, follow steps 3.5 and 3.6. If flash freezing the embryo, skip to step 3.8 immediately.</li>
	<li>If fixing the embryo for in situ hybridization, immediately add 4% PFA to the Petri dish to submerge the embryo. Drip 4% PFA directly onto the top of the embryo in order to flatten it; this prevents the embryo from curling. Fix the embryo in 4% PFA at 4 &#176;C for 12 hr.
	<ol>
		<li>After fixation, dehydrate embryos in graded methanol (MeOH) solutions and store at -20 &#176;C in 100% MeOH.</li>
	</ol>
	</li>
	<li>If the embryo is between stages 1 -&#160;822,&#160;remove the vitelline membrane adhered to the embryo.&#160;Note: This step can be done during or after fixation. Embryos younger than stage 822 are not easily visualized because they adhere to the vitelline membrane, obscuring key structures as seen in Figure 2A.
	<ol>
		<li>Grip the edge of the membrane that extends beyond the zone of junction with extra fine forceps. Carefully flip the embryo over multiple times to wash away residual yolk granules and to loosen the adherence of the embryonic disk to the vitelline membrane. Note: Do not touch the center of the embryo, as this will damage embryonic structures.</li>
		<li>If a gap does not appear between the zone of junction and the vitelline membrane, gently scratch the zone of junction with the extra fine tipped forceps to loosen it from the vitelline membrane. Grip the vitelline membrane with the extra fine tipped forceps and gently pull it away from the embryo. If necessary, gently pull the embryo away from the vitelline membrane by gripping the peripheral edge of the embryonic disk at the zone of junction.</li>
		<li>Discard the vitelline membrane in biohazard 1 waste (biosafety level 1) after removal.</li>
	</ol>
	</li>
	<li>When conducting an ISH assay on young embryonic stages, follow standard whole mount ISH protocols for chick embryos24, 25, but consider the following suggestions.
	<ol>
		<li>To reduce damage to the embryos during the ISH procedure, use a single 5 ml glass vial with a screw cap for each embryo. Only fill vials with 2 - 3 ml of solution, ensuring that the embryos are fully submerged. Nutate vials vertically by placing 5 ml vials into a styrofoam rack (or any rack that will keep the vials secure) that is secured to a nutator. Note: This precaution prevents the embryo from being torn, which can occur when it comes into contact with the lid of the vial during horizontal nutation.</li>
		<li>For embryos stage 0 - 622, treat with 5 &#956;g/ml proteinase K in 1X PTw for 5 min at room temperature. Treat embryos staged 7 - 1222 with 10 &#956;g/ml proteinase K in 1X PTw for 10 min at 37 &#176;C to reduce background staining.</li>
		<li>To produce a sufficient color reaction to detect low levels of gene expression in stages 1 - 1022, incubate with 10 &#956;g/ml probe concentration for 12 hr. For older stages, incubate with 1 &#956;g/ml probe concentration at 60 &#176;C.</li>
	</ol>
	</li>
	<li>If flash-freezing the embryo, quickly add 2 - 3 ml 1X PBS to the Petri dish following dissection and tilt the Petri dish to separate the embryo from the yolk granules.&#160;Remove liquid and repeat 2 - 3 times to remove all yolk. Using fine tipped forceps, transfer embryo to a pre-labeled microcentrifuge tube and flash freeze in liquid nitrogen before storing at -80 &#176;C.</li>
</ol>
4. EdU Cell Proliferation Assay. Incorporation and Detection of EdU in Zebra Finch Embryos.
<ol>
	<li>Candle the egg using a fiber optic illuminator lamp to locate the embryo or yolk.</li>
	<li>Mark the side of the egg opposite to the location of the embryo or yolk within the egg to ensure that the embryo is not damaged during the microinjection process.</li>
	<li>Line a 60 mm plastic dish with modeling clay and mold it in the shape of a bowl to hold the egg in the desired orientation. The marked spot should be oriented to allow insertion of the microinjection needle using the micromanipulator. Note: The clay will stabilize the egg during microinjection and throughout the incubation in step 4.11.</li>
	<li>Pull two glass capillary microinjection needles. Blunt one needle to poke a hole into the egg at the marked spot. Prepare the second microinjection needle for injection by backloading it with mineral oil and inserting it into the microinjector.</li>
	<li>Set the volume of solution released per injection to 59.8 nl on the microinjector.</li>
	<li>Load the microinjection needle with the 10 mM stock EdU solution.</li>
	<li>Create a hole in the shell on the marked spot with the blunted glass capillary, taking care to not shatter the shell or drop pieces of the shell into the egg cavity. Orient the egg so that the hole is at a 45&#176;&#160;angle, allowing the microinjection needle to be inserted directly through the cavity to the yolk or embryo.</li>
	<li>Using the micromanipulator, insert the loaded needle approximately 1.0 cm into the cavity.</li>
	<li>Inject the desired amount of the EdU solution directly onto the developing embryo or yolk. Note: A maximum of 478 nl of EdU can be injected without resulting in embryonic death.</li>
	<li>Immediately wrap the egg and the clay holder with multiple layers of plastic wrap to cover the egg and the dish to prevent desiccation of the embryo during incubation. Tape the edges of the plastic wrap to the bottom of the dish to prevent the plastic from unwrapping during incubation. Note: The plastic wrap should only be removed immediately before dissection.</li>
	<li>Allow the newly proliferating cells to incorporate the EdU by incubating the egg at 37 &#176;C until the desired stage is reached. After injection, do not return egg to tilting shelves in incubator. Place the plastic-wrapped clay lined dish on stable surface inside the incubator.</li>
	<li>Remove the plastic wrap and dissect the embryo following the aforementioned protocol. Fix the embryo in 4% PFA and incubate 12 hr at 4 &#176;C as described above. After fixation, wash with 100% ethanol (EtOH) for 5 min and store in fresh 100% EtOH at&#160;-20 &#176;C until further analysis.</li>
</ol>
5. EdU &#8220;Click&#8221; Reaction Protocol
The following steps are all performed in glass vials.
<ol>
	<li>Rehydrate embryos with successive 5 min washes of the following:</li>
	<li>EtOH, 75% EtOH and 25% sterile deionized distilled (sdd) water, 50% EtOH and 50% sdd water, 25% EtOH and 75% 1X PTw, 100% 1X Ptw</li>
	<li>Wash three times in 100% 1X PTw for 10 min each.</li>
	<li>Dilute the reaction buffer additive (Kit Component F) by combining 1 part of the 10X stock buffer solution (10 &#956;l) to 9 parts sdd water (90 &#956;l).</li>
	<li>Prepare the reaction mix in a separate tube by mixing the following: 875 &#956;l 1X PBS, 20 &#956;l CuSO4, 5 &#956;l azide, 100 &#956;l diluted reaction buffer additive. Note: Volume of the reaction mix can be scaled down. The reaction will work if the embryo is completely covered in the reaction mixture. Add the diluted reaction buffer additive (step 5.3) immediately before use. All subsequent steps are performed in the dark. Cover the embryos with foil to protect from the light.</li>
	<li>Cover the vials with aluminum foil, and incubate them vertically at room temperature for two hours by placing them in a styrofoam rack attached to a nutator.</li>
	<li>Wash the embryos 3 times in fresh 1X PBS for 10 min each.</li>
	<li>Incubate the embryos in fresh 4% PFA overnight at 4 &#176;C.</li>
	<li>Wash 3 times in 1X PBS for 10 min each and store in fresh 1X PBS at 4 &#176;C. Cover the embryos with foil until further analysis.</li>
</ol>

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B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adverse+effects+of+fipronil+on+avian+reproduction+and+development:+maternal+transfer+of+fipronil+to+eggs+in+zebra+finch+Taeinopygia+guttata+and+in+ovo+exposure+in+chickens+Gallus+domesticus.">Adverse effects of fipronil on avian reproduction and development: maternal transfer of fipronil to eggs in zebra finch Taeinopygia guttata and in ovo exposure in chickens Gallus domesticus.</a> Ecotoxicology. 20, 653-660 (2011).</li><li>Hallinger, K. K., Zabransky, D. J., Kazmer, K. A., Cristol, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Birdsong+differs+between+mercury-polluted+and+reference+sites.">Birdsong differs between mercury-polluted and reference sites.</a> The Auk. 127, 156-161 (2010).</li><li>Chen, C. C., Wada, K., Jarvis, E. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Radioactive+in+situ+Hybridization+for+Detecting+Diverse+Gene+Expression+Patterns+in+Tissue.">Radioactive in situ Hybridization for Detecting Diverse Gene Expression Patterns in Tissue.</a> Journal of Visualized Experiments. , (2012).</li><li>Chen, C. C., Balaban, E., Jarvis, E. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Interspecies+Avian+Brain+Chimeras+Reveal+That+Large+Brain+Size+Differences+Are+Influenced+by+Cell&#8211;Interdependent+Processes.">Interspecies Avian Brain Chimeras Reveal That Large Brain Size Differences Are Influenced by Cell&#8211;Interdependent Processes.</a> PLoS One. 7, (2012).</li><li>Chen, C. C., Winkler, C. M., Pfenning, A. R., Jarvis, E. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+profiling+of+the+developing+avian+telencephalon:+Regional+timing+and+brain+subdivision+continuities.">Molecular profiling of the developing avian telencephalon: Regional timing and brain subdivision continuities.</a> The Journal of Comparative Neurology. 521, 3666-3701 (2013).</li></ol>

The authors have nothing to disclose.

Recent development of an embryological staging guide22 and genome annotation make the zebra finch a desirable model organism for developmental studies. However, the small size and fragility of the zebra finch embryos, which range from 3 to 7 mm in stages 1 - 1022, can make dissections difficult11,14. Locating and cleanly removing embryos from the surface of the yolk can be challenging. This protocol provides sufficient detail to perform the procedure with ease. This protocol demonstrates the critical steps that are not typically known, but are necessary to ensure a successful dissection. For example, it is essential to leave a small layer of yolk between the embryo and sheet of weigh paper to preclude sticking.
Both the identification and removal of the embryo can be difficult. To troubleshoot identifying the embryo on the surface of the yolk, shine light directly above the yolk after it has been removed from the egg, and look at the yolk at a 45&#176; angle to find the embryo. Once the embryo is located, cut the yolk on weigh paper taking care to not tear the embryo.
If further applications include imaging for anatomical differences, in situ hybridization, or cell proliferation assays, it is important to remove the vitelline membrane in stage 1 - 822 for better visualization of structures. If experiencing difficulties when removing the yolk or the vitelline membrane in early stages, fix the embryo in 4 % PFA before washing it in 1X PBS to reduce embryonic fragility. By first removing the vitelline membrane during dissection as described, structures are clearly visible and intact in zebra finch embryos after performing an in situ hybridization.
A limitation of EdU is that administration of dosage volumes over 478 nl leads to embryonic fatality. However, the vast dosage range allows varying levels of proliferative cell tagging.
The &#8220;click&#8221; reaction used in this kit is the Copper(I)-Catalyzed-Alkyne-Azide-Cycloaddition (Cu(I)AAC). In this specific reaction, an alkyne-containing thymidine analogue molecule (EdU) is incorporated by actively dividing cells. The alkyne group in the EdU protrudes from the helical structure of the DNA, and is detected by exposure to an azide molecule conjugated to a green, fluorescent molecule which binds to the free alkyne group. The green fluorescence shows the newly proliferating cells in the embryo. The bio-orthogonality of the azide and the alkyne groups prevents non-specific staining because these reactive species are not naturally present in organisms. Also, because the DNA does not need to be denatured in order for the reaction to occur, further DNA-dependent analysis can be easily performed27.
An inherent limitation of this method is the small size and fragility of zebra finch embryos. Removing the vitelline membrane of embryos stages 1 - 1522 can result in damaging embryonic structures if not performed with caution. However, this protocol simplifies the dissection method, allowing investigators to use early embryonic stages to examine structural anomalies and gene expression that have not been previously studied in depth. This protocol opens the way for a plethora of cellular-molecular assays that will allow investigators to determine the developmental origins of adult phenotypes. For example, it will be possible to examine gene expression implicated in vocal learning under various environmental conditions or following pharmacological treatments at the earliest stages of development28,29,30,31. Although not demonstrated in this paper, this method potentially allows for other procedures such as radioactive in situ hybridization on zebra finch tissue sections and electroporation/in ovosurgery32,33,34. Given that the zebra finch has been established as an important model organism within a vast body of literature, such studies provide untapped opportunities to link developmental mechanisms with adult physiology and behavior, in particular the development of language7,9.

The overall goal of this technique is to obtain zebra finch (Taeniopygiaguttata) embryos from the earliest stages of embryogenesis for use in a wide range of developmental studies. Zebra finch have become the predominant songbird model organism and have been used extensively in a variety of fields, including toxicology1,2, behavior3, memory and learning4,5,6, comparative neuroanatomy7,8, and language development9,10. As the only songbird with a sequenced genome, the zebra finch allows molecular and genetic study of the Passeriformes order, which represents over 50% of known bird species11,12,13.
Despite the use of adult and juvenile zebra finch in a diverse array of fields, few studies have been performed on zebra finch embryos, particularly during early stages of development. This can be attributed to the small size of their eggs and embryos, and their newer status as a model organism14,15,16 for studies in which the chicken (Gallus gallusdomesticus) was previously used as a predominant model system17,18,19,20,21. However, as non-vocal learners, chickens are not an appropriate model system for studying the genetic basis of vocal learning, development of vocal learning, heritability, behavior, and the cortical-basal ganglia circuitry involved in motor learning10.
It is important to note that zebra finch embryos are much more delicate and more easily damaged than chick embryos during dissection and molecular procedures. In particular, greater care is required when performing permeabilization steps on zebra finch embryos. Strong detergents and enzymes that would not harm a chick embryo can damage zebra finch embryos. In terms of general care, it is necessary to put zebra finch eggs in small cups before placement in an incubator to prevent them from breaking when rolling during incubation.
Zebra finch are amenable to behavioral studies, easily and prolifically breed year-round in captivity, and are vocal learners. These characteristics allow the use of zebra finch to address the need for a model organism that integrates development, genetics, and behavioral aspects of language. The dissections methods detailed below, combined with a recently developed staging guide specific to zebra finch22,&#160;make the zebra finch an increasingly useful standardized developmental model organism. However, obtaining embryos at early stages can be daunting. This protocol allows investigators to easily obtain early stage embryos. Studies investigating the early development and the molecular developmental basis of complex behaviors in zebra finch, or the toxicological effects on development in other small, passerine birds will find this dissection methodology useful.

<table border="0" cellpadding="0" cellspacing="0" width="573">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Chicken egg incubator</td>
			<td style="width:71px;"></td>
			<td style="width:119px;"></td>
			<td style="width:167px;">We use a Picture Window Hova-Bator Incubator, Circulated Air Model&#160;&#160;&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Click-iT EdU Alexa Fluor 488 Imaging kit</td>
			<td>Invitrogen</td>
			<td>C10337</td>
			<td>Detection of cell proliferation.&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dissection microscope&#160;</td>
			<td></td>
			<td></td>
			<td>We use Olympus SZ61</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">7&#39;&#39; Drummond capillary for Nanoject II injector</td>
			<td>Drummond</td>
			<td>3-00-203-G/X</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Drummond Nanoject II microinjector</td>
			<td colspan="2">Drummond</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dumont Tweezers #55</td>
			<td>World Precision Instruments</td>
			<td align="right">14099</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Ethanol (EtOH)</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">50mL Falcon tube (polypropylene)</td>
			<td>Fisher Scientific</td>
			<td>06-443-18&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">FastPrep Lysis Matrix H tubes</td>
			<td>MP biomedicals</td>
			<td>6917-100</td>
			<td>Used for RNA extraction, used to homogenize embryos</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Fiber optic illuminator lamps (High Intensity Illuminator)</td>
			<td>Dolan-Jenner Industries&#160;</td>
			<td colspan="2">Fiber-Lite MI-150&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Glass vials with screw cap (DEPC treated)</td>
			<td>Fisher Scientific</td>
			<td>03-338A</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Microcentrifuge eppe tube (1.5 mL)</td>
			<td>Fisher Scientific</td>
			<td>05-408-129</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Mineral oil</td>
			<td>Sigma-Aldrich</td>
			<td>M-8410</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Modeling Clay</td>
			<td></td>
			<td></td>
			<td>Any brand</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Narshige PB-7 needle puller</td>
			<td>Narshige</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Omni Bead Ruptor Homogenizer</td>
			<td style="width:71px;">OMNI International</td>
			<td>19-010</td>
			<td>Used for RNA extraction</td>
		</tr>
		<tr height="25">
			<td colspan="3" height="25" style="height:25px;">4% Paraformaldehyde (4% PFA): 20 mL 8% PFA (32g paraformaldehyde, 350mL sdd H2O, adjust pH to 7.6, 400mL sdd H2O), 20mL 2xPBS</td>
			<td>Fixation of embryos. Caution, is harmful and do not inhale.&#160;</td>
		</tr>
		<tr height="25">
			<td colspan="4" height="25" style="height:25px;">Phosphate buffered saline (1xPBS): 200mL 10X PBS, 1800 mL Barnstead H2O, adjust pH to 7.4</td>
		</tr>
		<tr height="25">
			<td colspan="4" height="25" style="height:25px;">Phosphate buffered saline (10xPBS): 800mL Barnstead, 2.013g KCL, 80.063g NaCl, 2.722g KH2PO4 monobasic, 14.196g Na2HPO4 dibasic, 200mL Barnstead H2O, adjust pH to 6.5</td>
		</tr>
		<tr height="25">
			<td colspan="4" height="25" style="height:25px;">Phosphate buffered saline with 0.1% Tween-20 (1xPTw): 1800mL Barnstead H2O, 200mL 10X PBS, adjust pH to 7.4, 2mL Tween-20</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">35mL Plastic petri dish&#160;</td>
			<td>Fisher Scientific</td>
			<td>08-757-100A</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">plastic wrap</td>
			<td></td>
			<td></td>
			<td>Any brand</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Prepease RNA Spin Kit</td>
			<td>PrepEase, Affymetrix</td>
			<td>78766 1 KT</td>
			<td>Used for RNA extraction, used to homogenize embryos</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">Reaction Mix: 875&#956;L 1xPBS, 100mM 20&#956;L CuSO4 (Kit Component E), 5&#956;L Alexa Fluor 488 azide (Kit Component B), 100&#956;L diluted reaction buffer additive (Kit Component F)</td>
			<td>Invitrogen</td>
			<td>C10337</td>
			<td>Detection of cell proliferation.&#160;</td>
		</tr>
		<tr height="25">
			<td height="25" style="height:25px;">sdd H2O</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Seed cup&#160;</td>
			<td></td>
			<td></td>
			<td>We use it as a container when incubating eggs</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Stainless steel scalpel&#160;</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Standard nest box</td>
			<td></td>
			<td></td>
			<td>We use Abba Plastic Finch Nestboxes</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:216px;">4mL, Teflon Lined Cap, Glass Vials</td>
			<td>Fisher Scientific</td>
			<td>02-912-352</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Transfer pipettes (polyethylene)</td>
			<td>Fisher Scientific</td>
			<td>13-711-7M&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">4x4 weigh paper</td>
			<td>Fisher Scientific</td>
			<td>09-898-12B</td>
			<td></td>
		</tr>
	</tbody>
</table>

dissection and downstream analysis of zebra finch embryos at early stages of development

The zebra finch (Taeniopygiaguttata) has become an increasingly important model organism in many areas of research including toxicology1,2, behavior3, and memory and learning4,5,6. As the only songbird with a sequenced genome, the zebra finch has great potential for use in developmental studies; however, the early stages of zebra finch development have not been well studied. Lack of research in zebra finch development can be attributed to the difficulty of dissecting the small egg and embryo. The following dissection method minimizes embryonic tissue damage, which allows for investigation of morphology and gene expression at all stages of embryonic development. This permits both bright field and fluorescence quality imaging of embryos, use in molecular procedures such as in situ hybridization (ISH), cell proliferation assays, and RNA extraction for quantitative assays such as quantitative real-time PCR (qtRT-PCR).&#160;This technique allows investigators to study early stages of development that were previously difficult to access.

The steps diagrammed in Figure 1 indicate the appearance of the embryo while attached to the vitelline membrane (A) and demonstrate the proper method to separate the embryo from the yolk (B). The embryo can be identified by the zone of junction, which is much lighter than the vitelline membrane. The embryo itself is often difficult to distinguish until the yolk is cut away. Once the embryo is dissected from the egg, it can be fixed or flash frozen for future use. If an in situ hybridization is planned for the dissected embryo, it is necessary to remove the vitelline membrane that is adhered to the embryo via the zone of junction. Figure 2 illustrates the improved visibility of the embryo once this membrane is removed (C), and the proper way to peel the vitelline membrane (A, B). After dissection and fixation, whole mount in situ hybridization was performed as seen in Figure 3 (A, A&#8217;, B, B&#8217;) and Figure 4 (A, A&#39;, B, B&#8217;) and Figure 5 (A, B, C) to detect differences in orthodenticlehomeobox 2 (Otx2) expression in embryos developmentally exposed to low doses of methylmercury. Figure 5 shows sense probe results, demonstrating lack of background. In Figure 4, despite being dissected from the egg at the same time point, the embryo developmentally exposed to methylmercury (MeHg) progressed to stage 522 (B, B&#8217;), while the control embryo developed to stage 622 (A, A&#8217;). The group of embryos dissected and shown in Figure 4 were collected from the nest and taken from the incubator at the same times. Although some natural variation is present in development, based on previous dissection data, it is unlikely that temperature fluctuations in the incubator would cause only the 2.4 ppm methylmercury embryos to be developmentally delayed. The differences in stages indicate changes in cell proliferation in embryos developmentally exposed to methylmercury.
Before dissection, EdU was injected into a day 2 egg and allowed to incubate overnight. After dissection and fixation of the stage 1622 embryo, EdU was visualized using &#8220;click&#8221; chemistry, allowing detection of proliferating cells as seen in Figure 6 (A, B, C). It is important to carefully monitor time points when placing eggs in the incubator and during dissections, as exposure to methylmercury or performing the EdU assay may disrupt developmental progression. The earliest injection was performed on day 0, which was the day of collection as specified in step 1.3. This embryo was dissected approximately 38 hours later (stage 722). The survival rate was found to be approximately 90% (same rate as control embryos) as long as the injection amount was under 478 nl.
This dissection methodology also allows for high quality RNA extraction. After dissecting stage 1622 embryos, an RNA extraction was performed according to manufacturer&#8217;s protocol with no optimization required, as seen in Figure 7. The removal of the vitelline membrane was unnecessary for RNA extraction and later qRT-PCR applications.
Note: All embryo figures are oriented so that the anterior and posterior regions are at the top and bottom of the images, respectively. 
<img alt="Figure 1" src="/files/ftp_upload/51596/51596fig1highres.jpg" /> 
Figure 1.&#160;Procedure for locating and dissecting zebra finch embryos, stages 1-1022. Locate embryo by gently rolling the yolk until the faint white disk is apparent (A). Once the embryo is located at the center of the yolk, the yolk is dissected in a stepwise fashion (B) where the first cut relieves pressure of the vitelline membrane (1) and subsequent cuts (2) border the zone of junction (zj) which is adhered to the vitelline membrane. Scale bars represent 1 mm.
<img alt="Figure 2" src="/files/ftp_upload/51596/51596fig2highres.jpg" /> 
Figure 2. Removal of vitelline membrane and visibility of embryonic structures. Following removal of the embryo from the yolk, place embryo in a Petri dish containing 4% PFA. If an in situ hybridization needs to be performed, visibility of the embryonic structures is essential and can be achieved by removing the vitelline membrane (A). Grip the vitelline membrane with extra fine tipped forceps and gently peel it away from the embryo by handling the embryo directly at the outermost edge, if necessary (B). Vitelline membrane removal increases clarity of embryonic structures, and allows embryos to be imaged or processed with in situ hybridization (C). Scale bars represent 1 mm. <a href="https://www.jove.com/files/ftp_upload/51596/51596fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/51596/51596fig3highres.jpg" /> 
Figure 3. Whole mount in situ hybridization performed on zebra finch embryos developmentally exposed to methylmercury. Expression patterns of orthodenticlehomeobox 2 (Otx2) were characterized in embryos exposed to 0.0 ppm methylmercury (A, A&#8217;) and 2.4 ppm methylmercury (B, B&#8217;) via parental diet. The dorsal (A) and ventral (A&#8217;) expression of Otx2 is visible throughout the midbrain and optic vesicles during stage 1222. The treatment group embryos were dissected at the same time point, but were developmentally delayed as seen in the dorsal (B) and ventral (B&#8217;) view of head structures, which are characteristic of stage 1122. Abbreviations: mb, midbrain; op, optic vesicle. Scale bars represent 1 mm.
<img alt="Figure 4" src="/files/ftp_upload/51596/51596fig4highres.jpg" /> 
Figure 4.&#160;Whole mount&#160;in situ&#160;hybridization performed on zebra finch embryos developmentally exposed to methylmercury. Expression patterns of&#160;orthodenticlehomeobox 2 (Otx2)&#160;were characterized in stage 622 embryos exposed to 0.0 ppm methylmercury (A, A&#8217;) and stage 522 embryos exposed to 2.4 ppm methylmercury (B, B&#8217;) via parental diet. Abbreviations: am, anterior margin of mesoderm; no, notochord, notochord mesoderm; po, proamnion, anterior blastopore; ps, primitive streak22. Scale bars represent 1 mm.
<img alt="Figure 5" fo:content-width="6in" src="/files/ftp_upload/51596/51596fig5highres.jpg" width="600" /> 
Figure 5.&#160;Whole mount in situ&#160;hybridization performed on zebra finch embryos using sense probe. (A) Stage 522&#160;embryo. (B) Early stage 622 embryo. (C) Stage 1122 embryo. Scale bars represent 1 mm.
<img alt="Figure 6" src="/files/ftp_upload/51596/51596fig6highres.jpg" /> 
Figure 6.EdU incorporation and detection in zebra finch embryos. EdU &#8220;click&#8221; chemistry was used to detect proliferating cells in a stage 1622 embryo (A, B, C). EdU is incorporated into the DNA in the place of thymidine26,27 and is detected using click chemistry27. Proliferation is clearly visible in the lateral edges of the somites, and the tailbud. Panel A shows proliferation occurring exclusively in the posterior of the embryo and also shows individual proliferative cells. Panel B shows the proliferative locations in the whole embryo. Panel C shows the anterior region, and shows the highly proliferative telencephalon (te) in greater detail. Abbreviations: af, amniotic fold; flb, forelimb bud; hlb, hindlimb bud; le, lens vesicle; ms, mesencephalon; mt, metencephalon; opc, optic cup; pa, pharyngeal arch; sm, somite mesoderm; tb, tailbud; te, telencephalon. Scale bars represent 1 mm. <a href="https://www.jove.com/files/ftp_upload/51596/51596fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 7" src="/files/ftp_upload/51596/51596fig7highres.jpg" /> 
Figure 7.&#160;Quality of RNA extracted from dissected zebra finch embryos. Control (0.0 ppm) and 1.2 ppm methylmercury embryos were dissected and flash frozen as described in Step 3.8. Each lane shows RNA extracted from two homogenized embryos from each treatment group.

Watch this Scientific Journal Video about Dissection and Downstream Analysis of Zebra Finch Embryos at Early Stages of Development at JoVE.com

Dissection and Downstream Analysis of Zebra Finch Embryos at Early Stages of Development

The zebra finch (Taeniopygiaguttata) is a valuable model organism; however, early stages of zebra finch development have not been extensively studied. The protocol describes how to dissect early embryos for developmental and molecular applications.

The zebra finch (Taeniopygiaguttata) has become an increasingly important model organism in many areas of research including toxicology1,2, behavior3, and ...

dissection-downstream-analysis-zebra-finch-embryos-at-early-stages

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10.8K ビュー.  College of William and Mary. The zebra finch (Taeniopygiaguttata) is a valuable model organism; however, early stages of zebra finch development have not been extensively studied. The protocol describes how to dissect early embryos for developmental and molecular applications. 

ビデオ: Dissection and Downstream Analysis of Zebra Finch Embryos at Early Stages of Development

Dissection of 6.5 dpc Mouse Embryos

Analysis of gene expression patterns during early stages of mammalian embryonic development can provide important clues about gene function, cell-cell interaction and signaling mechanisms that guide embryonic patterning. However, dissection of the mouse embryo from the decidua shortly after implantation can be a challenging procedure, and detailed step-by-step documentation of this process is lacking.

Here we demonstrate how post-implantation (6.5 dpc) embryos are isolated by first dissecting the uterus of a pregnant mouse (detection of the vaginal plug was designated day 0.5 poist coitum) and subsequently dissecting the embryo from maternal decidua. The dissection of Reichert's membrane is described as well as the removal of the ectoplacental cone.

Isolation of postimplantation-stage embryos allows one to study gene patterning and analyze cell-lineage decision making processes during embryonic development, but proper dissection of the early embryo can be challenging. This protocol describes a method for isolating early primitive-streak-stage embryos (~6.5 days post coitum [dpc]).

Analysis of gene expression patterns during early stages of mammalian embryonic development can provide important clues about gene function, cell-cell ...

Preparation of Neuronal Cultures from Midgastrula Stage Drosophila Embryos

This video illustrates the procedure for making primary neuronal cultures from midgastrula stage Drosophila embryos. The methods for collecting embryos and their dechorionation using bleach are demonstrated. Using a glass pipet attached to a mouth suction tube, we illustrate the removal of all cells from single embryos. The method for dispersing cells from each embyro into a small (5 l) drop of medium on an uncoated glass coverslip is demonstrated. A view through the microscope at 1 hour after plating illustrates the preferred cell density. Most of the cells that survive when grown in defined medium are neuroblasts that divide one or more times in culture before extending neuritic processes by 12-24 hours. A view through the microscope illustrates the level of neurite outgrowth and branching expected in a healthy culture at 2 days in vitro. The cultures are grown in a simple bicarbonate based defined medium, in a 5% CO2 incubator at 22-24&deg;C. Neuritic processes continue to elaborate over the first week in culture and when they make contact with neurites from neighboring cells they often form functional synaptic connections. Neurons in these cultures express voltage-gated sodium, calcium, and potassium channels and are electrically excitable. This culture system is useful for studying molecular genetic and environmental factors that regulate neuronal differentiation, excitability, and synapse formation/function.

This video demonstrates the preparation of primary neuronal cultures from midgastrula stage Drosophila embryos. Views of live cultures show cells 1 hour after plating and differentiated neurons after 2 days of growth in a bicarbonate-based defined medium. The neurons are electrically excitable and form synaptic connections.

This video illustrates the procedure for making primary neuronal cultures from midgastrula stage Drosophila embryos. The methods for collecting embryos ...

Placing Growth Factor-Coated Beads on Early Stage Chicken Embryos

The neural tube expresses many proteins in specific spatiotemporal patterns during development. These proteins have been shown to be critical for cell fate determination, cell migration, and formation of neural circuits. Neuronal induction and patterning involve bone morphogenetic protein (BMP), sonic hedgehog (SHH), fibroblast growth factor (FGF), among others. In particular, the expression pattern of Fgf8 is in close proximity to regions expressing BMP4 and SHH. This expression pattern is consistent with developmental interactions that facilitate patterning in the telencephalon.

Here we provide a visual demonstration of a method in which an in ovo preparation can be used to test the effects of Fgfs in the formation of the forebrain. Beads are coated with protein and placed in the developing neural tube to provide sustained exposure. Because the procedure uses small, carefully placed beads, it is minimally invasive and allows several beads to be placed within a single neural tube. Moreover, the method allows for continued development so that embryos can be analyzed at a more mature stage to detect changes in anatomy and in neural patterning. This simple but useful protocol allows for real time imaging. It provides a means to make spatially and temporally limited changes to endogenous protein levels.

A variety of growth factors and proteins interact to induce cells to take on different cell fates during development. Here we demonstrate the use of an in ovo preparation to address possible interactions between different proteins in development by placing beads on E2.5 chick embryos.

The neural tube expresses many proteins in specific spatiotemporal patterns during development.   These proteins have been shown to be critical for cell ...

Method for Culture of Early Chick Embryos ex vivo (New Culture)

The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ideal tool for studying  the formation and patterning of brain, neural tube, somite and heart primordia. Applications of chick embryo culture include electroporation of DNA or RNA constructs in order to analyze gene function, grafts of growth factor coated beads such as FGFs and BMPs , as well as whole mount in situ hybridization and immunohistochemistry. This video demonstrates the different steps in chick embryo culture; First, the embryo is explanted in saline. Then, the embryo is centered on a glass ring. The membranes surrounding the embryo are lifted along the walls of the ring. The ring is then placed in a culture dish containing a pool of albumine. The culture dish is sealed and placed in a humid chamber, where the embryo is cultured for up to 24 hrs. Finally, the embryo is removed from the ring, fixed and processed for further applications. A troubleshooting guide is also presented.

Method for Culture of Early Chick Embryos ex vivo New Culture

This video demonstrates New culture, a method by which chick embryos are cultured outside the egg for up to 24 hr. This method enables one to study early development (primitive streak to 14 som.), a period corresponding to E7-9 in mouse. Applications of this technique include electroporation, in situ hybridization and immunohistochemistry.

The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ...

Double Whole Mount in situ Hybridization of Early Chick Embryos

The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ideal tool for studying  gene expression in brain, neural tube, somite and heart primordia formation. This video demonstrates the different steps in 2-color whole mount in situ hybridization; First, the embryo is dissected from the egg and fixed in paraformaldehyde. Second, the embryo is processed for prehybridization. The embryo is then hybridized with two different probes, one coupled to DIG, and one coupled to FITC.  Following overnight hybridization, the embryo is incubated with DIG coupled antibody. Color reaction for DIG substrate is performed, and the region of interest appears blue. The embryo is then incubated with FITC coupled antibody. The embryo is processed for color reaction with FITC, and the region of interest appears red. Finally, the embryo is fixed and processed for phtograph and sectioning. A troubleshooting guide is also presented.

This video demonstrates 2-color whole mount in situ hybridization, a method by which the spatial and temporal expression pattern of 2 different genes can be visualized in young chick embryos. This method was originally introduced by David Wilkinson, Domingos Henrique, Phil Ingham and David Ish -Horowicz.

A Neuronal and Astrocyte Co-Culture Assay for High Content Analysis of Neurotoxicity

High Content Analysis (HCA) assays combine cells and detection reagents with automated imaging and powerful image analysis algorithms, allowing measurement of multiple cellular phenotypes within a single assay. In this study, we utilized HCA to develop a novel assay for neurotoxicity. Neurotoxicity assessment represents an important part of drug safety evaluation, as well as being a significant focus of environmental protection efforts. Additionally, neurotoxicity is also a well-accepted in vitro marker of the development of neurodegenerative diseases such as Alzheimer's and Parkinson's diseases. Recently, the application of HCA to neuronal screening has been reported. By labeling neuronal cells with &beta;III-tubulin, HCA assays can provide high-throughput, non-subjective, quantitative measurements of parameters such as neuronal number, neurite count and neurite length, all of which can indicate neurotoxic effects. However, the role of astrocytes remains unexplored in these models. Astrocytes have an integral role in the maintenance of central nervous system (CNS) homeostasis, and are associated with both neuroprotection and neurodegradation when they are activated in response to toxic substances or disease states. GFAP is an intermediate filament protein expressed predominantly in the astrocytes of the CNS. Astrocytic activation (gliosis) leads to the upregulation of GFAP, commonly accompanied by astrocyte proliferation and hypertrophy. This process of reactive gliosis has been proposed as an early marker of damage to the nervous system. The traditional method for GFAP quantitation is by immunoassay. This approach is limited by an inability to provide information on cellular localization, morphology and cell number. We determined that HCA could be used to overcome these limitations and to simultaneously measure multiple features associated with gliosis - changes in GFAP expression, astrocyte hypertrophy, and astrocyte proliferation - within a single assay. In co-culture studies, astrocytes have been shown to protect neurons against several types of toxic insult and to critically influence neuronal survival. Recent studies have suggested that the use of astrocytes in an in vitro neurotoxicity test system may prove more relevant to human CNS structure and function than neuronal cells alone. Accordingly, we have developed an HCA assay for co-culture of neurons and astrocytes, comprised of protocols and validated, target-specific detection reagents for profiling &beta;III-tubulin and glial fibrillary acidic protein (GFAP). This assay enables simultaneous analysis of neurotoxicity, neurite outgrowth, gliosis, neuronal and astrocytic morphology and neuronal and astrocytic development in a wide variety of cellular models, representing a novel, non-subjective, high-throughput assay for neurotoxicity assessment. The assay holds great potential for enhanced detection of neurotoxicity and improved productivity in neuroscience research and drug discovery.

This article describes a novel protocol and reagent set designed for sensitive measurement of neurotoxic effects of compounds and treatments on co-cultures of neurons and astrocytes using high content analysis. Results demonstrate that high content analysis represents an exciting novel technology for neurotoxicity assessment.

High Content Analysis (HCA) assays combine cells and detection reagents with automated imaging and powerful image analysis algorithms, allowing ...

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds

In flowering plants, the embryo develops within a nourishing tissue - the endosperm - surrounded by the maternal seed integuments (or seed coat). As a consequence, the isolation of plant embryos at early stages (1 cell to globular stage) is technically challenging due to their relative inaccessibility. Efficient manual dissection at early stages is strongly impaired by the small size of young Arabidopsis seeds and the adhesiveness of the embryo to the surrounding tissues. Here, we describe a method that allows the efficient isolation of young Arabidopsis embryos, yielding up to 40 embryos in 1 hr to 4 hr, depending on the downstream application. Embryos are released into isolation buffer by slightly crushing 250-750 seeds with a plastic pestle in an Eppendorf tube. A glass microcapillary attached to either a standard laboratory pipette (via a rubber tube) or a hydraulically controlled microinjector is used to collect embryos from droplets placed on a multi-well slide on an inverted light microscope. The technical skills required are simple and easily transferable, and the basic setup does not require costly equipment. Collected embryos are suitable for a variety of downstream applications such as RT-PCR, RNA sequencing, DNA methylation analyses, fluorescence in situ hybridization (FISH), immunostaining, and reporter gene assays.

Efficient and Rapid Isolation of Early-stage Embryos from Arabidopsis thaliana Seeds

We report an efficient and simple method to isolate embryos at early stages of development from Arabidopsis thaliana seeds. Up to 40 embryos can be isolated in 1 hr to 4 hr, depending on the downstream application. The procedure is suitable for transcriptome, DNA methylation, reporter gene expression, immunostaining and fluorescence in situ hybridization analyses.

In flowering plants, the embryo develops within a nourishing tissue - the endosperm - surrounded by the maternal seed integuments (or seed coat). As a ...

A Protocol for Lentiviral Transduction and Downstream Analysis of Intestinal Organoids

Intestinal crypt-villus structures termed organoids, can be kept in sustained culture three dimensionally when supplemented with the appropriate growth factors. Since organoids are highly similar to the original tissue in terms of homeostatic stem cell differentiation, cell polarity and presence of all terminally differentiated cell types known to the adult intestinal epithelium, they serve as an essential resource in experimental research on the epithelium. The possibility to express transgenes or interfering RNA using lentiviral or retroviral vectors in organoids has increased opportunities for functional analysis of the intestinal epithelium and intestinal stem cells, surpassing traditional mouse transgenics in speed and cost. In the current video protocol we show how to utilize transduction of small intestinal organoids with lentiviral vectors illustrated by use of doxycylin inducible transgenes, or IPTG inducible short hairpin RNA for overexpression or gene knockdown. Furthermore, considering organoid culture yields minute cell counts that may even be reduced by experimental treatment, we explain how to process organoids for downstream analysis aimed at quantitative RT-PCR, RNA-microarray and immunohistochemistry. Techniques that enable transgene expression and gene knock down in intestinal organoids contribute to the research potential that these intestinal epithelial structures hold, establishing organoid culture as a new standard in cell culture.

In this video protocol we give a step by step explanation of lentiviral transduction in organoids of primary intestinal epithelium and of processing and downstream analysis of these cultures by quantitative RT-PCR, RNA-microarray and immunohistochemistry.

Intestinal crypt-villus structures termed organoids, can be kept in sustained culture three dimensionally when supplemented with the appropriate growth ...

Xenopus laevis as a Model to Identify Translation Impairment

Protein synthesis is a fundamental process to gene expression impacting diverse biological processes notably adaptation to environmental conditions. The initiation step, which involves the assembly of the ribosomal subunits at the mRNA initiation codon, involved initiation factor including eIF4G1. Defects in this rate limiting step of translation are linked to diverse disorders. To study the potential consequences of such deregulations, Xenopus laevis oocytes constitute an attractive model with high degrees of conservation of essential cellular and molecular mechanisms with human. In addition, during meiotic maturation, oocytes are transcriptionally repressed and all necessary proteins are translated from preexisting, maternally derived mRNAs. This inexpensive model enables exogenous mRNA to become perfectly integrated with an effective translation. Here is described a protocol for assessing translation with a factor of interest (here eIF4G1) using stored maternal mRNA that are the first to be polyadenylated and translated during oocyte maturation as a physiological readout. At first, mRNA synthetized by in vitro transcription of plasmids of interest (here eIF4G1) are injected in oocytes and kinetics of oocyte maturation by Germinal Vesicle Breakdown detection is determined. The studied maternal mRNA target is the serine/threonine-protein-kinase mos. Its polyadenylation and its subsequent translation are investigated together with the expression and phosphorylation of proteins of the mos signaling cascade involved in oocyte maturation. Variations of the current protocol to put forward translational defects are also proposed to emphasize its general applicability. In light of emerging evidence that aberrant protein synthesis may be involved in the pathogenesis of neurological disorders, such a model provides the opportunity to easily assess this impairment and identify new targets.

Xenopus laevis as a Model to Identify Translation Impairment

Protein synthesis control occurs mainly at the translation initiation step, deficiencies in which are linked to diverse disorders. To better understand their etiology, we described here a protocol using Xenopus laevis oocytes assessing the translation of mos transcript in the presence of a mutant of translation initiation factor eIF4G1.

Protein synthesis is a fundamental process to gene expression impacting diverse biological processes notably adaptation to environmental conditions. The ...

Visualizing the Early Stages of Phagocytosis

The mammalian body is equipped with various layers of mechanisms that help to defend itself from pathogen invasions. Professional phagocytes of the immune system &#8212; such as neutrophils, dendritic cells, and macrophages &#8212; retain the innate ability to detect and clear such invading pathogens through phagocytosis1. Phagocytosis involves choreographed events of membrane reorganization and actin remodeling at the cell surface2,3. Phagocytes successfully internalize and eradicate foreign molecules only when all stages of phagocytosis are fulfilled. These steps include recognition and binding of the pathogen by pattern recognition receptors (PRRs) residing at the cell surface, formation of phagocytic cup through actin-enriched membranous protrusions (pseudopods) to surround the particulate, and scission of the phagosome followed by phagolysosome maturation that results in the killing of the pathogen3,4.
Imaging and quantification of various stages of phagocytosis is instrumental for elucidating the molecular mechanisms of this cellular process. The present manuscript reports methods to study the different phases of phagocytosis. We describe a microscope-based approach to visualize and quantify the binding, phagocytic cup formation, and the internalization of particulate by phagocytes. As phagocytosis occurs when innate receptors on phagocytic cells encounter ligands on a target particle bigger than 0.5 &#181;m, the assays we present here comprise the use of pathogenic fungi Candida albicans and other particulates such as zymosan and IgG-coated beads.

Here we describe a microscope-based technique to visualize and quantify the early cascades of events during phagocytosis of pathogens such as the fungi Candida albicans and particulates that are larger than 0.5 &#181;m including zymosan and IgG-coated beads.

The mammalian body is equipped with various layers of mechanisms that help to defend itself from pathogen invasions. Professional phagocytes of the immune ...