This work was supported financially by NIH (1 R01 AI095338-01A1).

The authors declare that they have no competing financial interests.

Neutrophil migration across mucosal epithelial surfaces is a common feature in disease pathology following infection with bacterial pathogens3. The methodology described herein offers a rapid, straightforward approach to experimentally isolate this discrete event using a human cell derived in vitro coculture assay system that models a feature of the inflammatory process triggered by bacterial infections. This system was originally developed using polarized intestinal epithelial cells infected with ent...

Mucosal surfaces serve as physical and immunological barriers providing protection against external threats pervasive in the environment1,2.&#160;This protective epithelial barrier can be compromised when pathogenic organisms invade2.&#160;In the case of a bacterial pathogen, this encounter often instigates an inflammatory process by activating the innate immune system and triggering a rapid mobilization of first responder granulocytes known as neutrophils2-4. Chemotactic agents facilitating neutrophil recruitment are produced in part by the mucosal epithelial cells seeking to rid the host of the offending pathogen2-4.&#160;Excessive or unresolved neutrophil infiltration of the mucosal epithelial surface can cause significant pathology1,5.&#160;This is a consequence of nonspecific tissue damage caused by the anti-bacterial neutrophil arsenal5-7.&#160;In such cases, bacterial clearance capacity of neutrophils is overshadowed by destruction of host tissue during an infectious insult.&#160; Disruption of the protective epithelial barrier function can lead to enhanced exposure of underlying tissue to microorganisms and/or toxins, further exacerbating disease pathology8,9.&#160;These consequences can be observed in multiple organ systems including the lung and digestive tract1,5.&#160;Furthermore, noninfectious inflammatory conditions such as severe bouts of asthma, chronic obstructive pulmonary disease (COPD), acute respiratory distress syndrome (ARDS), and inflammatory bowel disease (IBD) are marked by the pathological breach of the mucosal epithelial barrier by an excessive neutrophilic response4,5,10-12.
The complex process of neutrophil recruitment following mucosal infection involves several compartmentalized steps1,5,13,14.&#160;First, neutrophils must depart from circulation via a series of cell-to-cell interactions that facilitate trans-endothelial migration1,13.&#160;Neutrophils next navigate existing interstitial space containing extracellular matrix1,14.&#160;To reach the lumen of the infected mucosa, neutrophils must then migrate across the epithelial barrier1,4,5.&#160;This intricate multistep phenomenon is often investigated in aggregate using in vivo animal models of infection15.&#160;Such models are useful for establishing the necessity of specific factors, such as chemokines, adhesion molecules, or signaling pathways that participate in the overall process but are largely inadequate for resolving molecular contributions critical for each distinct compartmentalized step16.&#160;Cocultured in vitro systems modeling trans-endothelial, trans-matrix, or trans-epithelial migration of neutrophils have been particularly useful in this regard1,14,16,17.&#160;
A robust coculture assay system has been developed for the purpose of deciphering mechanisms responsible for neutrophil trans-epithelial migration in response to pathogenic infection18-22.&#160;This model involves infecting the apical surface of polarized human epithelial cell layers with a bacterial pathogen followed by application of freshly isolated human neutrophils to the basolateral surface18-22.&#160;Neutrophils migrate across the epithelial barrier in response to epithelial-derived chemotactic products secreted following pathogenic infection18,21-23.&#160;This model system has been employed using intestinal and lung epithelial cultures exposed to appropriate tissue specific bacterial pathogens and has unveiled novel molecular mechanisms likely important to the neutrophil recruitment process during mucosal infection3,8,19,24-28.&#160;The strength of this in vitro coculture model is that a reductionist approach enables the investigator to experimentally manipulate the pathogen, epithelial barrier, and/or neutrophil in a well-controlled, highly reproducible, fairly inexpensive system.&#160;Insight gathered from this approach can be effectively leveraged to conduct focused analysis of compartmentalized events during neutrophil recruitment using in vivo infection models22,29,30.
This article demonstrates the multiple steps necessary for the successful establishment of this reproducible model to explore pathogen induced neutrophil trans-epithelial migration.&#160;Lung epithelial barriers infected with the pathogen Pseudomonas aeruginosa are featured in this article; however, other tissue epithelia and pathogens can be substituted with minor modifications.&#160;Seeding and culturing of polarized lung epithelial cell layers on inverted collagen coated permeable transwell filters is detailed herein, as is the growth of pathogenic P. aeruginosa and the isolation of neutrophils from whole blood.&#160;How these components are combined to observe pathogen induced neutrophil trans-epithelial migration is presented along with appropriate positive and negative controls to establish a reproducible assay.&#160;The versatility of this approach to examine various aspects of pathogen induced neutrophil trans-epithelial migration is discussed with reference to specific studies in the literature.

<table border="0" cellpadding="0" cellspacing="0" width="1470">
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	</colgroup>
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">NCl-H292 cells</td>
			<td style="width:147px;">ATCC</td>
			<td style="width:137px;">CRL-1848</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">RPMI-1640 medium</td>
			<td style="width:147px;">ATCC</td>
			<td style="width:137px;">30-2001</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Pseudomonas aeruginosa PAO1</td>
			<td style="width:147px;">ATCC</td>
			<td style="width:137px;">#47085</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Escherichia coli MC1000</td>
			<td style="width:147px;">ATCC</td>
			<td style="width:137px;">#39531</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">D-PBS (1x) liquid</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">14190-144</td>
			<td style="width:667px;">without calcium and magnesium</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Heat Inactivated Fetal bovine serum</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">10082-147</td>
			<td style="width:667px;">10% added to culture medium</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Penicillin-Streptomycin</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">15140-122</td>
			<td style="width:667px;">100x: 10,000 units of penicillin and 10,000 &#181;g of streptomycin per ml.</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Trypsin-EDTA (0.05%)</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">25300-062</td>
			<td style="width:667px;">50 ml aliquots are stored frozen at -20 &#186;C.&#160; Aliquot in use can be stored at 4 &#186;C short-term.&#160;&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Hank&#39;s Balanced Salt Solution - HBSS(-)</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">14175-079</td>
			<td style="width:667px;">Sterile, without calcium and magnesium</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Trypan Blue Solution</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">15250-061.</td>
			<td style="width:667px;">Stock = 0.4%</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Collagen, Rat Tail</td>
			<td style="width:147px;">Invitrogen</td>
			<td style="width:137px;">A10483-01</td>
			<td style="width:667px;">Can also be isolated in the laboratory directly from the tails of rats using standard protocols</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Citric acid</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">C1909-500G</td>
			<td style="width:667px;">Component of 1 M citrate buffer and acid citrate dextrose (ACD) solution</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Sodium Citrate</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">S4641-500G</td>
			<td style="width:667px;">Component of 1 M citrate buffer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Dextrose anhydrous</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">D8066-250G</td>
			<td style="width:667px;">Component of acid citrate dextrose (ACD) solution</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Ammonium Chloride</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">213330-500G</td>
			<td style="width:667px;">Component of red blood cell (RBC) lysis buffer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Sodium bicarbonate</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">S6014-500G</td>
			<td style="width:667px;">Component of red blood cell (RBC) lysis buffer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">EDTA</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">ED-100G</td>
			<td style="width:667px;">Component of red blood cell (RBC) lysis buffer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">HBSS(+) powder</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">H1387-10L</td>
			<td style="width:667px;">Key component of HBSS+</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">HEPES</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">H3375-500G</td>
			<td style="width:667px;">Component of HBSS+</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Sigmacote</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">SL2-25ML</td>
			<td style="width:667px;">Follow vendor instructions to coat glass pipette tips</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Triton X-100</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">T-9284</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">2,2&#39;-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS)</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">A9941-50TAB</td>
			<td style="width:667px;">Key component of ABTS substrate solution</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">30% Hydrogen Peroxide Solution</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">H1009-100ML</td>
			<td style="width:667px;">Component of ABTS substrate solution</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">N-Formyl-Met-Leu-Phe (fMLP or fMLF)</td>
			<td style="width:147px;">Sigma-Aldrich&#160;</td>
			<td style="width:137px;">F-3506</td>
			<td style="width:667px;">A Stock solution of 10 mM in DMSO should be prepared and aliquots stored at -20 &#186;C.</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Gelatin Type B</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">M-12026</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Pseudomonas isolation agar&#160;</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">DF0927-17-1</td>
			<td style="width:667px;">Follow manufacturer&#8217;s instructions to make PIA plates</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Ficoll-Paque PLUS&#160;</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">45-001-749</td>
			<td style="width:667px;">Optional, can improve neutrophil purity</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;"></td>
			<td style="width:147px;"></td>
			<td style="width:137px;"></td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;"></td>
			<td style="width:147px;"></td>
			<td style="width:137px;"></td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;"></td>
			<td style="width:147px;"></td>
			<td style="width:137px;"></td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;"></td>
			<td style="width:147px;"></td>
			<td style="width:137px;"></td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;"></td>
			<td style="width:147px;"></td>
			<td style="width:137px;"></td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Name of Material / Equipment</td>
			<td style="width:147px;">Company</td>
			<td style="width:137px;">Catalog Number</td>
			<td style="width:667px;">Comments</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">24-well migration plate</td>
			<td style="width:147px;">Corning Incorporated</td>
			<td style="width:137px;">#3524</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">24-well wash plate</td>
			<td style="width:147px;">Falcon</td>
			<td style="width:137px;">35-1147</td>
			<td style="width:667px;">Can be reused if soaked in 70% ethanol and washed thoroughly prior to reuse</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">96-well plate</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">#12565501</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:520px;">Transwell Permeable Supports&#160;</td>
			<td style="width:147px;">Corning Incorporated</td>
			<td style="width:137px;">#3415</td>
			<td style="width:667px;">Polycarbonate; Diameter: 6.5 mm; Growth area: 0.33 cm2; Dish style: 24-well plate; Pore size: 3.0 &#181;m</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Petri dish</td>
			<td style="width:147px;">Falcon</td>
			<td style="width:137px;">35-1013</td>
			<td style="width:667px;">Each Petri dish holds 24 inverted 0.33 cm2 Transwells.&#160;&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">500 ml 0.2 &#956;m filter / flask</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">09-740-25A</td>
			<td style="width:667px;">To sterilize acid citrate dextrose (ACD) solution</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">5-3/4 in glass Pasteur pipette</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">13-678-20A</td>
			<td style="width:667px;">Coat tips with Sigmacote prior to use</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Hemostat</td>
			<td style="width:147px;">Fisher Scientific</td>
			<td style="width:137px;">13-812-14</td>
			<td style="width:667px;">Curved, Serrated</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Invertoskop Inverted Microscope</td>
			<td style="width:147px;">Zeiss</td>
			<td style="width:137px;">#342222</td>
			<td style="width:667px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:520px;">Versa-Max Microplate Reader</td>
			<td style="width:147px;">Molecular Devices</td>
			<td style="width:137px;">#432789</td>
			<td style="width:667px;"></td>
		</tr>
	</tbody>
</table>

in vitro coculture assay to assess pathogen induced neutrophil trans-epithelial migration

Mucosal surfaces serve as protective barriers against pathogenic organisms.&#160;Innate immune responses are activated upon sensing pathogen leading to the infiltration of tissues with migrating inflammatory cells, primarily neutrophils.&#160;This process has the potential to be destructive to tissues if excessive or held in an unresolved state.&#160; Cocultured in vitro models can be utilized to study the unique molecular mechanisms involved in pathogen induced neutrophil trans-epithelial migration.&#160;This type of model provides versatility in experimental design with opportunity for controlled manipulation of the pathogen, epithelial barrier, or neutrophil.&#160;Pathogenic infection of the apical surface of polarized epithelial monolayers grown on permeable transwell filters instigates physiologically relevant basolateral to apical trans-epithelial migration of neutrophils applied to the basolateral surface.&#160;The in vitro model described herein demonstrates the multiple steps necessary for demonstrating neutrophil migration across a polarized lung epithelial monolayer that has been infected with pathogenic P. aeruginosa (PAO1).&#160;Seeding and culturing of permeable transwells with human derived lung epithelial cells is described, along with isolation of neutrophils from whole human blood and culturing of PAO1 and nonpathogenic K12 E. coli (MC1000).&#160; The emigrational process and quantitative analysis of successfully migrated neutrophils that have been mobilized in response to pathogenic infection is shown with representative data, including positive and negative controls.&#160;This in vitro model system can be manipulated and applied to other mucosal surfaces.&#160;Inflammatory responses that involve excessive neutrophil infiltration can be destructive to host tissues and can occur in the absence of pathogenic infections.&#160;A better understanding of the molecular mechanisms that promote neutrophil trans-epithelial migration through experimental manipulation of the in vitro coculture assay system described herein has significant potential to identify novel therapeutic targets for a range of mucosal infectious as well as inflammatory diseases.

Several studies have demonstrated that pathogen-infected epithelial layers facilitate neutrophil trans-epithelial migration3,8,19,24-28,31,32. This occurs via a pathogen-specific induction of an epithelial cell-derived neutrophil chemotactic gradient3,23. For example, pathogenic P. aeruginosa interacting with the apical surface of lung epithelial cells causes a substantial number of neutrophils to migrate across the epithelial layer18,22,25,26,33,34. This clinically relevant assa...

Watch this Scientific Journal Video about In vitro Coculture Assay to Assess Pathogen Induced Neutrophil Trans-epithelial Migration at JoVE.com

In vitro Coculture Assay to Assess Pathogen Induced Neutrophil Trans-epithelial Migration

Neutrophil trans-epithelial migration in response to mucosal bacterial infection contributes to epithelial injury and clinical disease.&#160;An in vitro model has been developed that combines pathogen, human neutrophils, and polarized human epithelial cell layers grown on transwell filters to facilitate investigations towards unraveling the molecular mechanisms orchestrating this phenomenon.

In vitro Coculture Assay to Assess Pathogen Induced Neutrophil Trans-epithelial Migration

Mucosal surfaces serve as protective barriers against pathogenic organisms.&#160;Innate immune responses are activated upon sensing pathogen leading to ...

in-vitro-coculture-assay-to-assess-pathogen-induced-neutrophil-trans

Research

JoVE Journal

Immunology and Infection

17.4K ビュー.  Harvard Medical School. 粘膜細菌感染に応答して好中球トランス上皮移動は、上皮損傷および臨床疾患に寄与する。この現象を調整する分子機構の解明に向けた研究を容易にするために、トランスウェルフィルター上で成長した病原体、ヒト好中球、偏光ヒト上皮細胞層を組み合わせた in vitro モデルが開発されました。

ビデオ: In vitro Coculture Assay to Assess Pathogen Induced Neutrophil Trans-epithelial Migration

Assay for Pathogen-Associated Molecular Pattern (PAMP)-Triggered Immunity (PTI) in Plants

To perceive potential pathogens in their environment, plants use pattern recognition receptors (PRRs) present on their plasma membranes. PRRs recognize conserved microbial features called pathogen-associated molecular patterns (PAMPs) and this detection leads to PAMP-triggered immunity (PTI), which effectively prevents colonization of plant tissues by non-pathogens1,2. The most well studied system in PTI is the FLS2-dependent pathway3. FLS2 recognizes the PAMP flg22 that is a component of bacterial flagellin. 
Successful pathogens possess virulence factors or effectors that can suppress PTI and allow the pathogen to cause disease1. Some plants in turn possess resistance genes that detect effectors or their activity, which leads to effector-triggered immunity (ETI)2.
We describe a cell death-based assay for PTI modified from Oh and Collmer4. The assay was standardized in N. benthamiana, which is being used increasingly as a model system for the study of plant-pathogen interactions5. PTI is induced by infiltration of a non-pathogenic bacterial strain into leaves. Seven hours later, a bacterial strain that either causes disease or which activates ETI is infiltrated into an area overlapping the original infiltration zone. PTI induced by the first infiltration is able to delay or prevent the appearance of cell death due to the second challenge infiltration. Conversely, the appearance of cell death in the overlapping area of inoculation indicates a breakdown of PTI. 
Four different combinations of inducers of PTI and challenge inoculations were standardized (Table 1). The assay was tested on non-silenced N. benthamiana plants that served as the control and plants silenced for FLS2 that were predicted to be compromised in their ability to develop PTI.

Assay for Pathogen-Associated Molecular Pattern PAMP-Triggered Immunity PTI in Plants

A cell death-based assay for PTI in Nicotiana benthamiana plants is described.

To perceive potential pathogens in their environment, plants use pattern recognition receptors (PRRs) present on their plasma membranes. PRRs recognize ...

Human T Lymphocyte Isolation, Culture and Analysis of Migration In Vitro

The migration of T lymphocytes involves the adhesive interaction of cell surface integrins with ligands expressed on other cells or with extracellular matrix proteins. The precise spatiotemporal activation of integrins from a low affinity state to a high affinity state at the cell leading edge is important for T lymphocyte migration 1. Likewise, retraction of the cell trailing edge, or uropod, is a necessary step in maintaining persistent integrin-dependent T lymphocyte motility 2. Many therapeutic approaches to autoimmune or inflammatory diseases target integrins as a means to inhibit the excessive recruitment and migration of leukocytes 3. To study the molecular events that regulate human T lymphocyte migration, we have utilized an in vitro system to analyze cell migration on a two-dimensional substrate that mimics the environment that a T lymphocyte encounters during recruitment from the vasculature. T lymphocytes are first isolated from human donors and are then stimulated and cultured for seven to ten days. During the assay, T lymphocytes are allowed to adhere and migrate on a substrate coated with intercellular adhesion molecule-1 (ICAM-1), a ligand for integrin LFA-1, and stromal cell-derived factor-1 (SDF-1). Our data show that T lymphocytes exhibit a migratory velocity of ~15 &mu;m/min. T lymphocyte migration can be inhibited by integrin blockade 1 or by inhibitors of the cellular actomyosin machinery that regulates cell migration 2.

Human T Lymphocyte Isolation, Culture and Analysis of Migration In Vitro

T lymphocyte migration occurs during homing to lymphoid organs, exit from the vasculature, and entering into peripheral tissues. Here, we describe a protocol that can be used to analyze T lymphocyte migration in vitro.

The migration of T lymphocytes involves the adhesive interaction of cell surface integrins with ligands expressed on other cells or with extracellular ...

Tracking Neutrophil Intraluminal Crawling, Transendothelial Migration and Chemotaxis in Tissue by Intravital Video Microscopy

The recruitment of circulating leukocytes from blood stream to the inflamed tissue is a crucial and complex process of inflammation1,2. In the postcapillary venules of inflamed tissue, leukocytes initially tether and roll on the luminal surface of venular wall. Rolling leukocytes arrest on endothelium and undergo firm adhesion in response to chemokine or other chemoattractants on the venular surface. Many adherent leukocytes relocate from the initial site of adhesion to the junctional extravasation site in endothelium, a process termed intraluminal crawling3. Following crawling, leukocytes move across endothelium (transmigration) and migrate in extravascular tissue toward the source of chemoattractant (chemotaxis)4. Intravital microscopy is a powerful tool for visualizing leukocyte-endothelial cell interactions in vivo and revealing cellular and molecular mechanisms of leukocyte recruitment2,5. In this report, we provide a comprehensive description of using brightfield intravital microscopy to visualize and determine the detailed processes of neutrophil recruitment in mouse cremaster muscle in response to the gradient of a neutrophil chemoattractant. To induce neutrophil recruitment, a small piece of agarose gel (~1-mm3 size) containing neutrophil chemoattractant MIP-2 (CXCL2, a CXC chemokine) or WKYMVm (Trp-Lys-Tyr-Val-D-Met, a synthetic analog of bacterial peptide) is placed on the muscle tissue adjacent to the observed postcapillary venule. With time-lapsed video photography and computer software ImageJ, neutrophil intraluminal crawling on endothelium, neutrophil transendothelial migration and the migration and chemotaxis in tissue are visualized and tracked. This protocol allows reliable and quantitative analysis of many neutrophil recruitment parameters such as intraluminal crawling velocity, transmigration time, detachment time, migration velocity, chemotaxis velocity and chemotaxis index in tissue. We demonstrate that using this protocol, these neutrophil recruitment parameters can be stably determined and the single cell locomotion conveniently tracked in vivo.

We describe a protocol of brightfield intravital microscopy for measuring dynamic neutrophil-endothelial cell interactions during neutrophil recruitment in response to the source of a neutrophil chemoattractant in vivo. Neutrophil intraluminal crawling, transendothelial migration and chemotaxis in mouse cremaster muscle tissue are visualized with time-lapsed video photography and tracked with ImageJ.

The recruitment of circulating leukocytes from blood stream to the inflamed tissue is a crucial and complex process of inflammation1,2. In the ...

Quantitative In vitro Assay to Measure Neutrophil Adhesion to Activated Primary Human Microvascular Endothelial Cells under Static Conditions

The vascular endothelium plays an integral part in the inflammatory response. During the acute phase of inflammation, endothelial cells (ECs) are activated by host mediators or directly by conserved microbial components or host-derived danger molecules. Activated ECs express cytokines, chemokines and adhesion molecules that mobilize, activate and retain leukocytes at the site of infection or injury. Neutrophils are the first leukocytes to arrive, and adhere to the endothelium through a variety of adhesion molecules present on the surfaces of both cells. The main functions of neutrophils are to directly eliminate microbial threats, promote the recruitment of other leukocytes through the release of additional factors, and initiate wound repair. Therefore, their recruitment and attachment to the endothelium is a critical step in the initiation of the inflammatory response. In this report, we describe an in vitro neutrophil adhesion assay using calcein AM-labeled primary human neutrophils to quantitate the extent of microvascular endothelial cell activation under static conditions. This method has the additional advantage that the same samples quantitated by fluorescence spectrophotometry can also be visualized directly using fluorescence microscopy for a more qualitative assessment of neutrophil binding.

Quantitative In vitro Assay to Measure Neutrophil Adhesion to Activated Primary Human Microvascular Endothelial Cells under Static Conditions

Neutrophil adherence to the activated endothelium at sites of infection is an integral component of the host's inflammatory response. Described in this report is a neutrophil binding assay that allows for the in vitro quantitation of primary human neutrophil binding to endothelial cells activated by inflammatory mediators under static conditions.

The vascular  endothelium plays an integral part in the inflammatory response. During the  acute phase of inflammation, endothelial cells (ECs) are ...

Quantitative Assessment of Human Neutrophil Migration Across a Cultured Bladder Epithelium

The recruitment of immune cells from the periphery to the site of inflammation is an essential step in the innate immune response at any mucosal surface. During infection of the urinary bladder, polymorphonuclear leukocytes (PMN; neutrophils) migrate from the bloodstream and traverse the bladder epithelium. Failure to resolve infection in the absence of a neutrophilic response demonstrates the importance of PMN in bladder defense. To facilitate colonization of the bladder epithelium, uropathogenic Escherichia coli (UPEC), the causative agent of the majority of urinary tract infections (UTIs), dampen the acute inflammatory response using a variety of partially defined mechanisms. To further investigate the interplay between host and bacterial pathogen, we developed an in vitro model of this aspect of the innate immune response to UPEC. In the transuroepithelial neutrophil migration assay, a variation on the Boyden chamber, cultured bladder epithelial cells are grown to confluence on the underside of a permeable support. PMN are isolated from human venous blood and are applied to the basolateral side of the bladder epithelial cell layers. PMN migration representing the physiologically relevant basolateral-to-apical direction in response to bacterial infection or chemoattractant molecules is enumerated using a hemocytometer. This model can be used to investigate interactions between UPEC and eukaryotic cells as well as to interrogate the molecular requirements for the traversal of bladder epithelia by PMN. The transuroepithelial neutrophil migration model will further our understanding of the initial inflammatory response to UPEC in the bladder.

We developed an in vitro model that mimics an important component of the acute inflammatory response during infection of the bladder with uropathogenic Escherichia coli. The transuroepithelial neutrophil migration assay enables quantitative assessment of human neutrophil migration across bladder epithelia, cultured on permeable supports, in response to bacterial infection or chemoattractant substances.

The recruitment of immune cells from the periphery to the site of inflammation is an essential step in the innate immune response at any mucosal surface. ...

Human Neutrophil Flow Chamber Adhesion Assay

Neutrophil firm adhesion to endothelial cells plays a critical role in inflammation in both health and disease. The process of neutrophil firm adhesion involves many different adhesion molecules including members of the &beta;2 integrin family and their counter-receptors of the ICAM family. Recently, naturally occurring genetic variants in both &beta;2 integrins and ICAMs are reported to be associated with autoimmune disease. Thus, the quantitative adhesive capacity of neutrophils from individuals with varying allelic forms of these adhesion molecules is important to study in relation to mechanisms underlying development of autoimmunity. Adhesion studies in flow chamber systems can create an environment with fluid shear stress similar to that observed in the blood vessel environment in vivo. Here, we present a method using a flow chamber assay system to study the quantitative adhesive properties of human peripheral blood neutrophils to human umbilical vein endothelial cell (HUVEC) and to purified ligand substrates. With this method, the neutrophil adhesive capacities from donors with different allelic variants in adhesion receptors can be assessed and compared. This method can also be modified to assess adhesion of other primary cell types or cell lines.

A method of quantitating neutrophil adhesion is reported. This method creates a dynamic flow environment similar to that encountered in a blood vessel. It allows the investigation of neutrophil adhesion to either purified adhesion molecules (ligand) or endothelial cell substrate (HUVEC) in a context similar to the in vivo environment with sheer stress.

Neutrophil firm adhesion to endothelial cells plays a critical role in inflammation in both health and disease. The process of neutrophil firm adhesion ...

Neutrophil Isolation and Analysis to Determine their Role in Lymphoma Cell Sensitivity to Therapeutic Agents

Neutrophils are the most abundant (40% to 75%) type of white blood cells and among the first inflammatory cells to migrate towards the site of inflammation. They are key players in the innate immune system and play major roles in cancer biology. Neutrophils have been proposed as key mediators of malignant transformation, tumor progression, angiogenesis and in the modulation of the antitumor immunity; through their release of soluble factors or their interaction with tumor cells. To characterize the specific functions of neutrophils, a fast and reliable method is coveted for in vitro isolation of neutrophils from human blood. Here, a density gradient separation method is demonstrated to isolate neutrophils as well as mononuclear cells from the blood. The procedure consists of layering the density gradient solution such as Ficoll carefully above the diluted blood obtained from patients diagnosed with chronic lymphocytic leukemia (CLL), followed by centrifugation, isolation of mononuclear layer, separation of neutrophils from RBCsby dextran then lysis of residual erythrocytes. This method has been shown to isolate neutrophils &#8805; 90 % pure. To mimic the tumor microenvironment, 3-dimensional (3D) experiments were performed using basement membrane matrix such as Matrigel. Given the short half-life of neutrophils in vitro, 3D experiments with fresh human neutrophils cannot be performed. For this reason promyelocytic HL60 cells are differentiated along the granulocytic pathway using the differentiation inducers dimethyl sulfoxide (DMSO) and retinoic acid (RA). The aim of our experiments is to study the role of neutrophils on the sensitivity of lymphoma cells to anti-lymphoma agents. However these methods can be generalized to study the interactions of neutrophils or neutrophil-like cells with a large range of cell types in different situations.

Neutrophils are the most abundant type of white blood cells. The isolation of neutrophils from human blood by density gradient separation method and the differentiation of human promyelocytic (HL60) cells along the granulocytic pathway are described here; to test their role on sensitivity of lymphoma cells to anti-lymphoma agents.

Neutrophils are the most abundant (40% to 75%) type of white blood cells and among the first inflammatory cells to migrate towards the site of ...

A Novel In Vitro Wound Healing Assay to Evaluate Cell Migration

The aim of this work is to show a novel method to evaluate the ability of some immunomodulatory molecules, such as antimicrobial peptides (AMPs), to stimulate cell migration. Importantly, cell migration is a rate-limiting event during the wound-healing process to re-establish the integrity and normal function of tissue layers after injury. The advantage of this method over the classical assay, which is based on a manually made scratch in a cell monolayer, is the usage of special silicone culture inserts providing two compartments to create a cell-free pseudo-wound field with a well-defined width (500 &#956;m). In addition, due to an automated image analysis platform, it is possible to rapidly obtain quantitative data on the speed of wound closure and cell migration. More precisely, the effect of two frog-skin AMPs on the migration of bronchial epithelial cells will be shown. Furthermore, pretreatment of these cells with specific inhibitors will provide information on the molecular mechanisms underlying such events.

A Novel In Vitro Wound Healing Assay to Evaluate Cell Migration

Here, we present a protocol to evaluate the effect of peptides on the migration of bronchial epithelial cells. This method allows for the rapid and highly reproducible obtainment of quantitative data on the speed of cell migration and wound closure.

The aim of this work is to show a novel method to evaluate the ability of some immunomodulatory molecules, such as antimicrobial peptides (AMPs), to ...

Analysis of Shear Flow-induced Migration of Murine Marginal Zone B Cells In Vitro

Marginal zone B cells (MZBs) are a population of B cells that reside in the mouse splenic marginal zones that envelop follicles. To reach the follicles, MZBs must migrate up the shear force of blood flow. We present here a method for analyzing this flow-induced MZB migration in vitro. First, MZBs are isolated from the mouse spleen. Second, MZBs are settled on integrin ligands in flow chamber slides, exposed to shear flow, and imaged under a microscope while migrating. Third, images of the migrating MZBs are processed using the MTrack2 automatic cell tracking plugin for ImageJ, and the resulting cell tracks are quantified using the Ibidi chemotaxis tool. The migration data reveal how fast the cells move, how often they change direction, whether the shear flow vector affects their migration direction, and which integrin ligands are involved. Although we use MZBs, the method can easily be adapted for analyzing migration of any leukocyte that responds to the force of shear flow.

Marginal zone B cells (MZBs) respond to the force of shear flow by re-orienting their migration path up the flow. This protocol shows how to record and analyze the migration using a fluidics unit, pump, microscope imaging system, and free software.

Marginal zone B cells (MZBs) are a population of B cells that reside in the mouse splenic marginal zones that envelop follicles. To reach the follicles, ...

A High-throughput Assay to Assess and Quantify Neutrophil Extracellular Trap Formation

Neutrophil extracellular traps (NETs) are immunogenic extracellular DNA structures that can be released by neutrophils upon a wide variety of triggers. NETs have been demonstrated to serve as an important host defense mechanism that traps and kills microorganisms. On the other hand, they have been implicated in diverse systemic autoimmune diseases. NETs are immunogenic and toxic structures that contain a pool of relevant autoantigens including anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV) and systemic lupus erythematosus (SLE). Different forms of NETs can be induced depending on the stimulus. The amount of NETs can be quantified using different techniques including measuring DNA release in supernatants, measuring DNA-complexed with NET-molecules like myeloperoxidase (MPO) or neutrophil elastase (NE), measuring the presence of citrullinated histones by fluorescence microscopy, or flow cytometric detection of NET-components which all have different features regarding their specificity, sensitivity, objectivity, and quantity. Here is a protocol to quantify ex vivo NET formation in a highly-sensitive, high-throughput manner by using three-dimensional immunofluorescence confocal microscopy. This protocol can be applied to address various research questions about NET formation and degradation in health and disease.

This protocol describes a highly sensitive and high throughput neutrophil extracellular trap (NET) assay for the semi-automated quantification of ex vivo NET formation by immunofluorescence three-dimensional confocal microscopy. This protocol can be used to evaluate NET formation and degradation after different stimuli and can be used to study potential NET-targeted therapies.

Neutrophil extracellular traps (NETs) are immunogenic extracellular DNA structures that can be released by neutrophils upon a wide variety of triggers. ...