Name: an endothelial planar cell model for imaging immunological synapse dynamics
Uploaded: 2015-12-24T13:00:00
Description: Watch this Scientific Journal Video about An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics at JoVE.com

We thank Dr. Peter T. Sage for his assistance in generating some of the representative images. This work was supported by an NIH R01 grant to C.V.C. (HL104006).

All experiments described in this protocol are conducted with primary human T cells and commercially available primary human endothelial cells (dermal or lung microvascular ECs).Any research protocol involving human subjects must be approved by an institutional review board and written informed consent must be provided from each blood donor. Experiments conducted using this protocol were approved by the IRB of Beth Israel Deaconess Medical Center.
1. Preparing Human CD4+ Th1 Effector/Memory T Cells
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Overall, this protocol describes methods for investigating endothelial cells as i) understudied physiologic APCs and ii) as a novel type of &#39;planar cellular APC model&#39;. With respect to the former, it has become increasingly appreciated that non-hematopoietic peripheral (or &#39;stromal&#39;) APCs play critical, non-redundant roles (i.e., compared to hematopoietic APCs) in shaping adaptive immune responses 16-18. Among such &#39;semi-professional&#39; APCs, vascular and lymphatic endothelial ce...

T lymphocytes are a branch of the adaptive immune system characterized by the ability to efficiently recognize peptide antigen (Ag) bound to major histocompatibility complex (MHC) molecules through their T cell receptors (TCRs) 1. Na&#239;ve lymphocytes constitutively migrate and scan &#39;professional Ag presenting cells&#39; (APCs; e.g., dendritic cells) within lymph nodes, while memory/effector T cells need to effectively survey an extremely wide range of APCs and potential target cells within peripheral tissues.
In the min following initial recognition of cognate Ag on an APC, lymphocytes arrest their migration and begin to form a specialized intimate cell-cell interface termed &#39;immunological synapse&#39; (IS). Sustained (i.e., 30-60 min) IS contacts are required to amplify and sustain signaling 2-7. Emerging studies identify that within the IS, it is the continuous formation and rapid remodeling of discrete sub-cellular signaling micro-clusters (i.e., containing MHC/Ag-TCR, F-actin, adhesion and signaling molecules) that determine the strength and quality of resulting immune responses 2-7. However, dynamic details and regulatory mechanism of this process are incompletely understood 8,9. This stems largely from technical challenges associated with irregular topologies of APC surfaces and poorly controlled orientation of the cell-cell interaction planes, issues that profoundly limit the requisite spatiotemporal imaging approaches 8-10 (Figure1A).
<img alt="Figure 1" src="/files/ftp_upload/53288/53288fig1.jpg" />
Figure 1.&#160;A Physiologic Planar Cell APC Model for Imaging Immunological Synapse Dynamics. The schematic illustrates traditional imaging of immunological synapse between a T cell and a professional APC (A) and T cell and a traditional planar lipid bilayer APC model (B) in comparison to this novel endothelial planar APC model (C). Professional APCs provide physiologic immunological synapses but offer poorly oriented cell-cell interface (i.e., with respect to the optimal x-y imaging plane; resolution ~0.2 &#956;m), which dramatically compromises spatial (z imaging plane resolution ~1 &#956;m) and temporal (i.e., due to the need to repeatedly scan through all z imaging planes) resolution of imaging. Bilayer models have a planar topology that provides optimal spatiotemporal imaging resolution, but are also highly simplified, non-physiological and rigid. This endothelial cell model combines the planar topology of lipid bilayers with the physiologic substrate of a classic APC to deliver optimal spatial and temporal imaging resolution in a physiologic setting. <a href="https://www.jove.com/files/ftp_upload/53288/53288fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Previous work has partially circumvented these obstacles by developing planar substrate models (i.e., lipid bilayers and antibody-coated surfaces) that provide optimal spatiotemporal resolution (i.e., via fixing the T cell activation surface into a single plan that is parallel to the optimal x-y imaging plane) 11-15 (Figure 1B). These models have facilitated important insights into the subcellular/molecular dynamics that control antigenic signaling in T cells, including the discovery of dynamic actin/TCR signaling micro-clusters 7,11-14. However, such models are inherently oversimplified, as well as rigid (precluding the development/study of 3-dimensional topological features) (Figure 1B). Therefore, it remains uncertain how to relate such findings to physiologic cell-cell immune surveillance.
Though still understudied, vascular and lymphatic endothelial cells are emerging as a large (i.e., greater in numbers than all professional APCs, by ~1,000-fold) peripheral compartment of &#39;semi-professional&#39; APCs 16-18. These cells express MHC-I-, MHC-II- and a multitude of co-stimulator molecules (e.g., CD40, LFA3, ICOSL, 4-1BB, OX40L, TL1A, PD-L1; but not CD80 and CD86) and are strategically positioned at the blood-tissue interface where they serve specialized sentinel functions 16-18. Previous studies demonstrated that endothelial cells can effectively re-stimulate effector/memory, but not na&#239;ve, T cells 19-25. Thus, endothelial cells are likely to play unique APC roles in effector phase of adaptive immune responses within the peripheral tissues, such as local influence on T cell activation, differentiation, memory and tolerance 16,17,26. Critically, when grown in vitro, endothelial cells form virtually planar cell surfaces and are readily transfectable (e.g., with fluorescent protein reporters). These features are ideal for high spatiotemporal resolution imaging of topological dynamics during cell-cell interactions 19,27. Thus endothelial cells might serve as a physiologic &#39;planar cellular APC&#39; model distinctly suited for the study of the subcellular/molecular remodeling mechanisms that drive antigen recognition and regulate responses (Figure 1C) 19,20.
Previously established complementary imaging techniques (including transfection of endothelia cells with fluorescent protein makers of the plasma membrane and cytosol) for studying the details of leukocyte-endothelial interaction during adhesion and transendothelial migration 27, showed that leukocytes actively probe the surface of the endothelium by dynamic insertion and retraction of sub-micron-scale, actin-rich cylindrical protrusions (~200-1,000 nm in diameter and depth) termed invadosome-like protrusions (i.e., &#39;ILPs&#39;) 27,28. These imaging approaches have been further expanded along with the creation of protocols to take advantage of endothelial APC function to develop the first methods for high spatiotemporal resolution imaging of the T cell-endothelial immunological synapse as reported 19,20 and further describe herein. A central finding derived from this novel planar cellular APC model is that T cell ILPs function both in promoting initial Ag detection and in sustaining subsequent signaling. Indeed, arrays of multiple ILPs (that were stabilized and accrued in response to initial calcium flux) show enrichment in TCR and molecules suggestive of active signaling such PKC-Q, ZAP-70, phosphotyrosine and HS1. Therefore, ILPs seem to represent a three-dimensional physiologic equivalent to the TCR-signaling microclusters seen in planar bilayer models. This approach, thus, sensitively reveals/reports molecular and architectural (and implied biomechanical) dynamics not otherwise detectable.
The method described herein should be useful to bridging the gap between professional APC and artificial APC substrate models in order to enhance our ability to interrogate basic mechanisms of adaptive immune responses. While here the focus is on the activation of CD4+ Th1-type effector/memory cell, this basic approach can be readily modified to study a wide range of T cell types and Ags, as discussed below.

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	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">BD Vacutainer stretch latex free tourniquet</td>
			<td style="width:149px;">BD Biosciences</td>
			<td style="width:152px;">367203</td>
			<td style="width:221px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">BD alcohol swabs</td>
			<td style="width:149px;">BD Biosciences</td>
			<td>326895</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">BD Vacutainer Safety-Lok</td>
			<td style="width:149px;">BD Biosciences</td>
			<td style="width:152px;">367861</td>
			<td>K2 EDTA</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">BD Vacutainer Push Button Blood Collection Set</td>
			<td style="width:149px;">BD Biosciences</td>
			<td style="width:152px;">367335</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">RPMI-1640</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>R8758-1L</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Ficoll-Paque&#160;</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td style="width:152px;">GE17-1440-02</td>
			<td>Bring to RT before use</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">FCS-Optima</td>
			<td style="width:149px;">Atlanta Biologics</td>
			<td>s12450</td>
			<td>Heat inactivated</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Penicillin-Streptomycin&#160;</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>&#160;P4458-100ML&#160;&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Trypan blue</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>T8154-20ML</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">staphylococcal enterotoxin B&#160;</td>
			<td>Toxin Technology</td>
			<td>BT202RED</td>
			<td>Stock solution 1mg/ml in PBS</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">toxic shock syndrome toxin 1&#160;</td>
			<td>Toxin Technology</td>
			<td>TT606RED</td>
			<td>Stock solution 1mg/ml in PBS</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">human IL-15</td>
			<td style="width:149px;">R&#38;D Systems</td>
			<td>247-IL-025</td>
			<td>Stock solution 50ug/ml in PBS</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">PBS</td>
			<td>Life Technologies</td>
			<td>10010-049</td>
			<td></td>
		</tr>
		<tr height="26">
			<td height="26" style="height:26px;width:392px;">Fibronectin</td>
			<td style="width:149px;">Life Technologies</td>
			<td>33016-015</td>
			<td>Stock solution 1mg/ml in H20</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">HMVEC-d Ad-Dermal MV Endo Cells</td>
			<td style="width:149px;">Lonza</td>
			<td>CC-2543</td>
			<td>Other Human Microvascular ECs can be used, i.e. HLMVECs</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">EGM-2 MV bullet kit</td>
			<td style="width:149px;">Lonza</td>
			<td>CC-3202</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Trypsin-EDTA</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>T-4174</td>
			<td>Stock solution 10x, dilute in PBS</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">amaxa-HMVEC-L Nucleofector Kit</td>
			<td style="width:149px;">Lonza</td>
			<td>vpb1003</td>
			<td>Required Kit for step 4</td>
		</tr>
		<tr height="26">
			<td height="26" style="height:26px;width:392px;">IFN-g</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>I3265</td>
			<td>Stock solution 1mg/ml in H20</td>
		</tr>
		<tr height="26">
			<td height="26" style="height:26px;">TNF-alpha 10ug, human</td>
			<td style="width:149px;">Life Technologies</td>
			<td>PHC3015</td>
			<td>Stock solution 1mg/ml in H20</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">phenol Red-free HBSS&#160;</td>
			<td style="width:149px;">Life Technologies</td>
			<td>14175-103</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Hepes</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>BP299-100</td>
			<td></td>
		</tr>
		<tr height="26">
			<td height="26" style="height:26px;width:392px;">Calcium Chloride</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td style="width:152px;">C1016-100G</td>
			<td>Stock solution 1M in H20</td>
		</tr>
		<tr height="26">
			<td height="26" style="height:26px;width:392px;">Magnesium chloride</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td style="width:152px;">208337</td>
			<td>Stock solution 1M in H20</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Human Serum albumin</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td>A6909-10ml</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Immersol 518 F fluorescence free Immersion oil</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>12-624-66A</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Fura-2 AM 20x50ug</td>
			<td style="width:149px;">Life Technologies</td>
			<td>F1221</td>
			<td>Stock solution 1mM in DMSO</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">pEYFP-Mem (Mem-YFP)</td>
			<td style="width:149px;">Clontech</td>
			<td style="width:152px;">6917-1</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">pDsRed-Monomer (Soluble Cytoplasmic DsRed)</td>
			<td style="width:149px;">Clontech</td>
			<td style="width:152px;">632466</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">pDsRed-Monomer Membrane (Mem-DsRed)</td>
			<td style="width:149px;">Clontech</td>
			<td style="width:152px;">632512</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">pEGFP-Actin</td>
			<td style="width:149px;">Clontech</td>
			<td style="width:152px;">6116-1</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Alexa Fluor 488 Phalloidin</td>
			<td style="width:149px;">Life Technologies</td>
			<td>A12379</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Formaldehyde solution 37%</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>BP531-500</td>
			<td>Toxic, use fumehood</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Triton X-100</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td style="width:152px;">X100-5ML</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">&#160;Falcon 15mL Conical Centrifuge Tubes</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>14-959-70C</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Falcon 50mL Conical Centrifuge Tubes</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>14-959-49A&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Falcon Tissue Culture Treated Flasks T25</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>10-126-9</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">&#160;Falcon Tissue Culture Treated Flasks T75</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>&#160; 13-680-65</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">&#160;Corning Cell Culture Treated T175</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td style="width:152px;">10-126-61&#160;</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Glass coverslips&#160;</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td style="width:152px;">12-545-85&#160;</td>
			<td>12 mm diameter</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">&#160;Falcon Tissue Culture Plates 24-well</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>08-772-1</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Delta-T plates</td>
			<td style="width:149px;">Bioptechs</td>
			<td>04200415B</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Wheaton Disposable Pasteur Pipets</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td style="width:152px;">13-678-8D</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">1.5 ml Eppendorf tube&#160;</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td>05-402-25</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">&#160;ICAM1 mouse anti-human</td>
			<td style="width:149px;">BD Biosciences</td>
			<td>555509</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">HS1 mouse anti-human</td>
			<td>BD Biosciences</td>
			<td>610541</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Anti-Human CD11a (LFA-1alpha) Purified</td>
			<td>ebioscience</td>
			<td>BMS102</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Anti-Human CD3 Alexa Fluor&#174; 488</td>
			<td>ebioscience</td>
			<td>53-0037-41</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Anti-MHC Class II antibody&#160;</td>
			<td style="width:149px;">Abcam</td>
			<td>ab55152</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Anti-Talin 1 antibody</td>
			<td style="width:149px;">Abcam</td>
			<td>ab71333</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Anti-PKC theta antibody&#160;</td>
			<td style="width:149px;">Abcam</td>
			<td>ab109481</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">phosphotyrosine (4G10 Platinum)</td>
			<td style="width:149px;">Millipore</td>
			<td>50-171-463</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Nucleofector II</td>
			<td style="width:149px;">Amaxa Biosystems</td>
			<td style="width:152px;"></td>
			<td>Required electroporator for step 4</td>
		</tr>
		<tr height="41">
			<td height="41" style="height:41px;width:392px;">Zeiss Axiovert</td>
			<td style="width:149px;">Carl Zeiss MicroImaging</td>
			<td style="width:152px;"></td>
			<td></td>
		</tr>
		<tr height="41">
			<td height="41" style="height:41px;width:392px;">Zeiss LSM510&#160;</td>
			<td style="width:149px;">Carl Zeiss MicroImaging</td>
			<td style="width:152px;"></td>
			<td></td>
		</tr>
		<tr height="41">
			<td height="41" style="height:41px;width:392px;">Zeiss Axiovison Software</td>
			<td style="width:149px;">Carl Zeiss MicroImaging</td>
			<td style="width:152px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">NU-425 (Series 60) Biological Safety Cabinet</td>
			<td style="width:149px;">NuAIRE</td>
			<td style="width:152px;">Nu-425-600</td>
			<td></td>
		</tr>
		<tr height="41">
			<td height="41" style="height:41px;width:392px;">&#160;Forma STRCYCLE 37 &#176;C, 5% CO2 Cell culture Incubator</td>
			<td>Fisher Scientific</td>
			<td>202370</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Centrifuge 5810</td>
			<td style="width:149px;">Eppendorf</td>
			<td style="width:152px;">EW-02570-02</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Hemocytometer</td>
			<td style="width:149px;">Sigma-Aldrich</td>
			<td style="width:152px;">&#160;Z359629</td>
			<td>Bright-Line Hemocytometer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:392px;">Isotemp Waterbath model 202</td>
			<td style="width:149px;">Fisher Scientific</td>
			<td style="width:152px;">15-462-2</td>
			<td></td>
		</tr>
	</tbody>
</table>

an endothelial planar cell model for imaging immunological synapse dynamics

Adaptive immunity is regulated by dynamic interactions between T cells and antigen presenting cells (&#39;APCs&#39;) referred to as &#39;immunological synapses&#39;. Within these intimate cell-cell interfaces discrete sub-cellular clusters of MHC/Ag-TCR, F-actin, adhesion and signaling molecules form and remodel rapidly. These dynamics are thought to be critical determinants of both the efficiency and quality of the immune responses that develop and therefore of protective versus pathologic immunity. Current understanding of immunological synapses with physiologic APCs is limited by the inadequacy of the obtainable imaging resolution. Though artificial substrate models (e.g., planar lipid bilayers) offer excellent resolution and have been extremely valuable tools, they are inherently non-physiologic and oversimplified. Vascular and lymphatic endothelial cells have emerged as an important peripheral tissue (or stromal) compartment of &#39;semi-professional APCs&#39;. These APCs (which express most of the molecular machinery of professional APCs) have the unique feature of forming virtually planar cell surface and are readily transfectable (e.g., with fluorescent protein reporters). Herein a basic approach to implement endothelial cells as a novel and physiologic &#39;planar cellular APC model&#39; for improved imaging and interrogation of fundamental antigenic signaling processes will be described.

A novel imaging approach using endothelial cells and combining the resolution advantages of the planar lipid bilayers model with the physiologic complexity and deformability of professional APCs was developed (Figure 1). Figure 2 provides examples of typical migration, calcium flux and topological dynamics observed with this approach. In the absence of SAg on endothelium, SAg-specific CD4+ Th1 lymphocytes rapidly spread, polarize and laterally ...

Watch this Scientific Journal Video about An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics at JoVE.com

An Endothelial Planar Cell Model for Imaging Immunological Synapse Dynamics

Adaptive immunity is controlled by dynamic 'immunological synapses' formed between T cells and antigen presenting cells. This protocol describes methods for investigating endothelial cells both as understudied physiologic APCs and as a novel type of 'planar cellular APC model'.

Adaptive immunity is regulated by dynamic interactions between T cells and antigen presenting cells (&#39;APCs&#39;) referred to as &#39;immunological ...

Research

JoVE Journal

Immunology and Infection

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Visualization of the Immunological Synapse by Dual Color Time-gated Stimulated Emission Depletion (STED) Nanoscopy

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Real-time Imaging of Endothelial Cell-cell Junctions During Neutrophil Transmigration Under Physiological Flow

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Super-resolution Imaging of the Natural Killer Cell Immunological Synapse on a Glass-supported Planar Lipid Bilayer

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Opsonophagocytic Killing Assay to Assess Immunological Responses Against Bacterial Pathogens

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