Name: imaging cd4 t cell interstitial migration in the inflamed dermis
Uploaded: 2016-03-25T14:00:00
Description: Watch this Scientific Journal Video about Imaging CD4 T Cell Interstitial Migration in the Inflamed Dermis at JoVE.com

作者感谢罗切斯特多光子显微镜核心设施的大学与实时成像帮助。支持NIH AI072690和AI02851到DJF; AI114036以股份公司和AI089079到MGO。

所有涉及小鼠的程序是由罗切斯特大学的机构动物护理和使用委员会批准，并严格按照动物福利法和人文关怀和实验动物的使用公共卫生服务政策由国家机构管理的实施卫生，实验室动物福利办公室。 1.效应CD4 + T细胞的制备注：特异性识别从鸡蛋卵清蛋白（：ISQAVHAAHAEINEAGR POVA）肽BALB / c小鼠TCR转基因小鼠DO11.10。其他TCR转基因系统可以被取代，使用适当的?...

意义 这里，我们提出一个完整的协议为传输，抗原特异性效应Th1细胞在完整小鼠耳真皮4D可视化。此方法提供了以下几个原因一些当前成像模式的优点。通过成像腹耳真皮，我们能够放弃所需的涉及其他部位皮肤成像方案脱毛。虽然脱毛剂通常是温和的，它们已被证明导致破坏皮肤屏障42，这个过程可以刺激免疫应答43,44。还通过避免侵入外科手术以暴...

The effector function of CD4 T cells is critically dependent on their ability to rapidly enter and traverse a wide variety of peripheral tissues to survey for damage, locate foci of infection, or cause pathology from chronic infection or autoimmunity. While the processes of homing to inflamed sites1-4 and extravasation5-7 from the vasculature into tissues have been well-characterized, the factors that drive and regulate the interstitial motility of T cells remain undefined. The migration of T cells in complex 3D environments has been studied in vitro through the use of artificial matrices8-10 or microfluidic devices11,12, but these fail to recapitulate the complex and dynamic environment of an in vivo system. It is only recently, with the advent of high-resolution multi-color intravital imaging that it has become possible to study the dynamic behavior of immune cells in situ, allowing for a better understanding of intact immune responses.
Over a decade ago, several influential studies were published that first utilized multiphoton microscopy to address immunological questions. Early studies focused on the behavior of immune cells within explanted lymphoid organs13-16, which were soon followed by techniques to image exposed lymph nodes in anesthetized mice17. Imaging allowed for new fundamental observations about the stages of lymph node priming of T cells18, the mechanisms by which T cells migrate in secondary lymphoid organs19, T cell interactions with other immune cells20,21, and dynamic T cell positioning within the lymph node22. Although many early studies focused on lymph node dynamics, intravital imaging has been since been utilized to image the immune response in many peripheral tissues, including the brain23-25, liver26, lung27, and skin28-30. 
The mouse ear dermis is particularly well poised for imaging, due to the thinness of ear skin, a relative lack of hair, and the ease with which it can be isolated from respiratory movements31. Indeed, the ear dermis has been used to image the interstitial behavior of dendritic cells32,33, T cells28,29,34,35, and neutrophils36,37, and is a well-established site for studying dermal inflammation. Increasingly, non-invasive procedures have been replacing surgical preparations of the skin, including split dermis38,39, flank39,40, or dorsal skin flap window39,41 models, that can induce changes to the local inflammatory milieu. The use of transferred, in vitro-primed, antigen-specific CD4 effector T cells allows for the study of a homogenous population of cells in the context of a dermal inflammatory response30. Here we describe a non-invasive imaging procedure that allows for the visualization of antigen-specific effector CD4 T cells in the dermal interstitium of the inflamed mouse ear, and the ability to manipulate these cells in real-time by introducing blocking antibodies through a venous catheter. We show that this model is effective for tracking the movement of CD4 T cells in the dermis and for querying the mechanisms that govern this motility.

<table border="0" cellpadding="0" cellspacing="0" width="1060">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">BALB/c mice</td>
			<td style="width:145px;">Jackson Laboratories</td>
			<td style="width:196px;">000651</td>
			<td style="width:472px;">Mice used were bred in-house</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">DO11.10 mice</td>
			<td>Jackson Laboratories</td>
			<td>003303</td>
			<td>Mice used were bred in-house</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">HBSS</td>
			<td>Fisher</td>
			<td>10-013-CV</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Newborn Calf Serum (NCS)</td>
			<td>Thermo/HyClone</td>
			<td>SH30118.03</td>
			<td>Heat inactivated at 56 &#176;C for 30 minutes</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Guinea Pig Complement</td>
			<td>Cedarlane</td>
			<td>CL-5000</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-CD8 antibody</td>
			<td>ATCC</td>
			<td>3.155 (ATCC TIB-211)</td>
			<td>Antibodies derived from&#160; this hybridoma</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-MHC Class II antibody</td>
			<td>ATCC</td>
			<td>M5/114.15.2 (ATCC TIB-120)</td>
			<td>Antibodies derived from&#160; this hybridoma</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-CD24 antibody</td>
			<td>ATCC</td>
			<td>J11d.2 (ATCC TIB-183)</td>
			<td>Antibodies derived from&#160; this hybridoma</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-Thy1.2 antibody</td>
			<td>ATCC</td>
			<td>J1j.10 (ATCC TIB-184)</td>
			<td>Antibodies derived from&#160; this hybridoma</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Ficoll (Fico/Lite-LM)</td>
			<td>Atlanta Biologicals</td>
			<td>I40650</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">PBS</td>
			<td>Fisher</td>
			<td>21-040-CV</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">EDTA</td>
			<td>Fisher</td>
			<td>15323591</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">biotinylated anti-CD62L antibody (clone MEL-14)</td>
			<td>BD</td>
			<td>553149</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">streptavidin magnetic separation beads</td>
			<td>Miltenyi</td>
			<td>130-048-101</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">MACS LS Separation Column</td>
			<td>Miltenyi</td>
			<td>130-042-401</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">recombinant human IL-2</td>
			<td>Peprotech</td>
			<td>200-02</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">recombinant mouse IL-4</td>
			<td>Peprotech</td>
			<td>214-14</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">recombinant mouse IL-12</td>
			<td>Peprotech</td>
			<td>210-12</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-IFNg antibody (clone XMG 1.2)</td>
			<td>eBioscience</td>
			<td>16-7311-85</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">anti-IL-4 antibody (clone 11b11)</td>
			<td>eBioscience</td>
			<td>16-7041-85</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">RPMI</td>
			<td>VWR</td>
			<td>45000-412</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Penicillin/Streptomycin</td>
			<td>Fisher</td>
			<td>15303641</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">L-glutamine</td>
			<td>Fisher</td>
			<td>15323671</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">2-mercaptoethanol</td>
			<td>Bio-Rad</td>
			<td>161-0710</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">ovalbumin peptide</td>
			<td>Biopeptide</td>
			<td></td>
			<td>ISQAVHAAHAEINEAGR-OH peptide</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Fetal Calf Serum (FCS)</td>
			<td>Thermo/HyClone</td>
			<td>SV30014.03</td>
			<td>Heat inactivated at 56 &#176;C for 30 minutes</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">24-well culture plate</td>
			<td>LPS</td>
			<td>3526</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">CFSE</td>
			<td>Life Technologies</td>
			<td>C34554</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">CMTMR</td>
			<td>Life Technologies</td>
			<td>C2927</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">28 G1/2 insulin syringes, 1ml</td>
			<td>BD</td>
			<td>329420</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">28 G1/2 insulin syringes, 300&#956;l</td>
			<td>BD</td>
			<td>309301</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">27 G1/2 TB syringes, 1ml</td>
			<td>BD</td>
			<td>309623</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">30 G1/2 needles</td>
			<td>BD</td>
			<td>305106</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">PE-10 medical tubing</td>
			<td>BD</td>
			<td>427400</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">cyanoacrylate veterinary adhesive (Vetbond)</td>
			<td>3M</td>
			<td>1469SB</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">heating plate</td>
			<td>WPI</td>
			<td>61830</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Heating plate controller</td>
			<td>WPI</td>
			<td>ATC-2000</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Water blanket controller</td>
			<td>Gaymar</td>
			<td>TP500</td>
			<td>No longer in production, newer equivalent available</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">water blanket</td>
			<td>Kent Scientific</td>
			<td>TP3E</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Isoflurane vaporizer</td>
			<td>LEI Medical</td>
			<td>Isotec 4</td>
			<td>No longer in production, newer equivalent available</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">isoflurane</td>
			<td>Henry Schein</td>
			<td></td>
			<td>Ordered through Veterinary staff</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">microcentrifuge tubes</td>
			<td>VWR</td>
			<td>20170-038</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">medical tape</td>
			<td>3M</td>
			<td>1538-0</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">isoflurane nosecone</td>
			<td></td>
			<td></td>
			<td>Built In-house, see Fig 2</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">imaging platform</td>
			<td></td>
			<td></td>
			<td>Built In-house, see Fig 2</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">curved forceps</td>
			<td>WPI</td>
			<td>15915-G</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">scissors</td>
			<td>Roboz</td>
			<td>RS-6802</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">glass coverslips</td>
			<td>VWR</td>
			<td></td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">high vacuum grease</td>
			<td>Fisher</td>
			<td>146355D</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">cotton swabs</td>
			<td></td>
			<td></td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">delicate task wipes</td>
			<td>Fisher</td>
			<td>34155</td>
			<td>Multiple Equivalent</td>
		</tr>
		<tr height="84">
			<td height="84" style="height:84px;width:247px;">Olympus Fluoview 1000 AOM-MPM upright microscope with Spectra-Physics MaiTai HP DeepSee Ti:Sa laser</td>
			<td>Olympus</td>
			<td></td>
			<td>call for quote</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">optical table with vibration control</td>
			<td>Newport</td>
			<td></td>
			<td>call for quote</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">25x NA 1.05 water immersion objective for multiphoton imaging</td>
			<td>Olympus</td>
			<td>XLPLN25XWMP2</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">objective heater</td>
			<td>Bioptechs</td>
			<td>PN 150815</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Detection filter cube</td>
			<td>Olympus</td>
			<td>FV10-MRVGR/XR</td>
			<td>Proprietary cube, can be approximated from individual filters/dichroics</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">anti-integrin &#946;1 antibody (clone hMb1-1)</td>
			<td>eBioscience</td>
			<td>16-0291-85</td>
			<td>Azide free, low endotoxin</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:247px;">anti-integrin &#946;3 antibody (clone 2C9.G3)</td>
			<td>eBioscience</td>
			<td>16-0611-82</td>
			<td>Azide free, low endotoxin</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">Texas Red Dextran (70,000 MW)</td>
			<td>Life Technologies</td>
			<td>D-1830</td>
			<td></td>
		</tr>
	</tbody>
</table>

imaging cd4 t cell interstitial migration in the inflamed dermis

CD4 + T细胞进行的效应子功能的能力取决于通过一个尚未未定义机制这些细胞在发炎外周组织的迅速和有效的迁移。多光子显微镜对免疫系统的研究中的应用提供了测量的完整组织内的免疫应答的动力学的工具。这里，我们提出在发炎的小鼠耳真皮的CD4 T细胞的非侵入性活体多光子成像的协议。使用定制成像平台和静脉导管允许的CD4 T细胞动力学在真皮间质的可视化，通过加入阻断抗体中涉及能动性关键分子组分来询问这些细胞中的实时的能力。该系统提供了在体外模型和微创手术成像程序既有优势。了解的CD4 T细胞的活力所使用的途径，最终可能提供洞察到基CD4 + T细胞的C函数以及自身免疫性疾病的慢性感染的发病机制和病理。

研究原位免疫反应，而不改变免疫环境的能力是研究与发炎组织T效应细胞的实时交互必需的。由这个协议中，在图1A和B中概述的完好耳真皮的成像，允许转移荧光标记的T效应细胞在皮肤间质的可视化。这允许两个高分辨率（ 图1C）和延时（ 图1D， 电影1）在发炎的真皮效应T细胞动力学的图片。 <p cl...

Watch this Scientific Journal Video about Imaging CD4 T Cell Interstitial Migration in the Inflamed Dermis at JoVE.com

Imaging CD4 T Cell Interstitial Migration in the Inflamed Dermis

成像的CD4 T细胞间质迁移发炎真皮

支配CD4效应T细胞的间质动力在炎症部位的机制比较陌生。我们提出了一种非侵入性的方式来可视化和体外 -primed CD4T细胞操纵在发炎耳朵真皮，允许这些细胞在原位的动态行为的研究。

The ability of CD4 T cells to carry out effector functions is dependent upon the rapid and efficient migration of these cells in inflamed peripheral ...

The overall goal of this imaging protocol is to visualize CD4 positive T Cell dynamics in the inflamed skin. This method can help answer key questions in the field of immunology, such as, what are the mechanisms that underlie immune cell motility, and function in inflamed tissues. The main advantage of this technique, is that it provides a minimally invasive way to study CD4 T cell dynamic behavior In Situ.Visual demonstration of this method is critical, as the steps to prepare the ear for imaging are difficult to learn, and proper positioning of the ear is necessary to capture high quality images. I'm Alison Gaylo, a graduate student, and I will be doing the demonstration of this protocol. Begin by aspirating 300 microliters of fluorescently labeled effector T cell suspension per mouse into a syringe equipped with a 27 and a half gauge needle.Then turn the syringe needle side up, and gently flick the shaft of the syringe, moving the plunger up and down as necessary to remove any bubbles. When the cells are ready, transfer the mice into a clean cage, and place them under a heat lamp, until the tail veins are vasodilated. Then transfer the first mouse into the restrainer, and wipe the tail with an alcohol swab.After identifying a lateral tail vein, slowly inject 200 microliters of cells into the vein. When all of the cells have been transferred, draw 50 microliters of complete fluorescens emulsion into a 28 and a half gauge insulin syringe and press down firmly on the plunger to remove any large air bubbles. Then place a thimble on the left index finger, and carefully grasp the mouse's ear between the left thumb and thimble, with the ventral ear facing up.Then slide the needle, bevel side up, into the dermis in the outer third of the pinna, and slightly off center, and slowly inject ten microliters of emulsion into the tissue. After injecting all of the animals, monitor the mice until they are fully recovered. Three days following the immunization, vasodilate the tail veins of the injected animals as just demonstrated.After anesthetizing, immobilize the tail of the first mouse with a pair of forceps. Wipe the tail with an alcohol swab, then carefully slide a 30 and a half gauge needle catheter into a lateral tail vein, checking for patency by gentle pressure to the syringe plunger. When the catheter is in place, apply one to two drops of cyanoacrylate tissue adhesive to the injection site, and allow the adhesive to dry for approximately 30 seconds.Then use scissors to carefully trim the whiskers and the hair from the back and sides of the ear. Next, use a cotton swab to moisten the inner surface of the ear with PBS. Then rotate the mouse, and flatten the injected ear onto a 24 by 50 millimeter number one point five glass cover slip, until it is flush with the glass.Blot away the excess PBS. Then use two pairs of curved forceps to grasp an approximately 20 millimeter long piece of fabric tape lengthwise at the top corners, and place the bottom of the tape onto the cover slip at the top of the mouse's ear. Roll the tape over the rest of the ear, pushing the excess hair out of the way with the forceps as necessary, and use a dry cotton swab to gently press the tape around the ear to ensure a tight seal, taking care not to press on the ear itself.It is essential that the ear is taped properly to the cover slip with a good seal on both sides and with minimal air bubbles, as this will affect the quality of the images that can be obtained. Now tape a fluorescent microscope imaging platform to a 37 degree Celsius heating block, and apply vacuum grease to both sides of the ear area of the platform. Rotate the mouse to place the cover slip onto the platform, taking care to align the ear in the center of the felt.When the ear is in place, snap the isoflurane nose cone into the holder on the platform, ensuring that the cone is secure, and completely covering the mouse's nose. Then use a cotton swab to firmly, but carefully, press the cover slip onto the imaging platform, spreading the vacuum grease under the cover slip. Wrap two 20 millimeter pieces and two longer pieces of tape around the upper portion of the platform to affix the cover slip to the platform.Next, move the mouse to the microscope stage. Secure the platform with more tape, and pipe a double layer of vacuum grease onto the cover slip around the ear. Then wrap a water filled heating blanket around the mouse, and fill the vacuum grease reservoir with 37 degrees Celsius distilled water.For In Vivo time lapse imaging, begin by positioning the objective over the center of the ear, and lower the objective until it just contacts the surface of the water in the reservoir. Next, using an external light source, slowly lower the objective until the surface of the ear comes into focus. Then, lower the inner and outer curtains around the microscope stage, and adjust the laser wave length to 900 nanometers in the MP laser controller window, the laser power in the acquisition setting laser window, and the PMT voltages in the image acquisition control window.In the acquisition setting size and mode windows, set the microscope to five twelve by five twelve pixel resolution, with a two microsecond per pixel dwell time, and select XY repeat to activate a live imaging mode for scanning through the tissue. Once an appropriate imaging field has been located, locate the highest cell in the dermis, and click the set zero button to set the Z position to zero. Scroll down in the Z direction to measure the extent of the cell depth.Then set the starting and end positions in the acquisition setting microscope window, and adjust the instrument PMT voltages and laser power in the bright Z window to optimize the visualization of the cells throughout the depth of the imaging field. Check the depth and time buttons, and set a common filter to scan the image three times per line in the image acquisition control filter mode window. Adjust the Z slice depth in the image acquisition microscope window so that it takes approximately one minute to capture a complete stack as noted in the time view window.Then, to assess the stability of the tissue, set the number of repeats to five in the acquisition setting time scan window, and click the scan button to capture a five minute time lapse image of the area. If the tissue is stable after five minutes, set the number of repeats to between 30 and 45 in the acquisition setting time scan window, and collect a 30 to 45 minute time lapse image, monitoring for any minor tissue drift as the image is collected. Save the pre-antibody image in the appropriate format, and then draw the antibody mixture into a one milliliter tuberculin syringe, taking care to remove all of the air bubbles.Gently press the plunger so that the antibody solution forms a droplet at the end of the needle, and lift the curtains around the stage to locate the catheter. Replace the PBS syringe with the syringe of antibody, and then slowly inject the antibodies into the catheter. When the antibodies have been successfully injected, re-lower the curtains and note the time of injection.Then immediately start collecting a new 20 to 40 minute imaging sequence, in the same location, using the same instrument settings as the pre-antibody image. Finally, save the post-antibody image file in the appropriate format, and carefully remove the mouse from the microscope stage, monitoring the animal until it is fully recovered. Imaging of the intact ear dermis by this protocol facilitates the acquisition of high resolution and time lapse images of effector T cell dynamics in the inflamed dermis.In this movie, the green adoptively transferred effector T cells can be observed moving throughout the dermal tissue. After the administration of antibeta one and antibeta three entogrin blocking antibodies through the catheter, however, the previously motile cells arrest within the dermis. The cells exhibit a decreased average velocity after antibody administration as well as a significant decrease in their meandering index.That is, the ration of the total displacement to the total track length. Autofluorescents from hair follicles, shadowing and autofluorescents from overlying hair, and air bubbles trapped between the ear surface and the cover slip, can all lead to imaging artifacts, which obscure the visualization of the T cells, and interfere with the automated image analysis software. In addition, using multiple sources of heat can cause tissue stability issues, leading to large oscillations during imaging that make interpreting the results difficult.Once mastered, imaging the CD4 T cells in the dermis can be completed in two to three hours, if the procedure has been performed correctly. While attempting this procedure, it's important to remember to follow the appropriate animal care and use guidelines for working with mice. This procedure can be adapted to visualize other T cell subsets or types of immune cells in the ear, using different models of infect, or different methods of inducing inflammation.After its development, intravital imaging paved the way for researchers in the field of immunology, to explore the dynamics of ongoing immune responses in living animals. Don't forget that working with a multi-phosphor laser can be extremely hazardous and that precautions, such as proper shielding, should always be taken while performing this procedure. After watching this video, you should have a good understanding of how to induce inflammation in a mouse ear dermis, how to use intravital imaging to capture the time lapse images of CD4 T cell activity before and after antibody administration.

Research

JoVE Journal

Immunology and Infection

Retroviral Transduction of T-cell Receptors in Mouse T-cells

T细胞受体在小鼠T细胞的逆转录病毒转导

T-cell receptors (TCRs) play a central role in the immune system. TCRs on T-cell surfaces can specifically recognize peptide antigens presented by antigen ...

科研

免疫与感染

Competitive Homing Assays to Study Gut-tropic T Cell Migration

竞争的原点实验研究肠嗜T细胞迁移

In order to exert their function lymphocytes need to leave the blood and migrate into different tissues in the body. Lymphocyte adhesion to endothelial ...

A Quantitative Evaluation of Cell Migration by the Phagokinetic Track Motility Assay

细胞迁移的的Phagokinetic轨道运动MLCK的定量评价

Cellular motility is an important biological process for both unicellular and multicellular organisms. It is essential for movement of unicellular ...

Real-time Live Imaging of T-cell Signaling Complex Formation

T细胞实时成像实时信号复合物的形成

Protection against infectious diseases is mediated by the immune system 1,2. T lymphocytes are the master coordinators of the immune system, regulating ...

Monitoring Dendritic Cell Migration using 19F / 1H Magnetic Resonance Imaging

Monitoring Dendritic Cell Migration using 19F / 1H Magnetic Resonance Imaging

监测树突状细胞迁移<sup&gt; 19</sup&gt; F /<sup&gt; 1</sup&gt; H磁共振成像

Continuous  advancements in noninvasive imaging modalities such as magnetic resonance  imaging (MRI) have greatly improved our ability to study ...

Isolation and Th17 Differentiation of Na&iuml;ve CD4 T Lymphocytes

Isolation and Th17 Differentiation of Na&#239;ve CD4 T Lymphocytes

隔离和幼稚的CD4 T细胞的Th17细胞分化

Th17 cells are a distinct subset of T cells that have been found to produce interleukin 17 (IL-17), and differ in function from the other T cell subsets ...

In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function

In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function

在体外试验 ，以评估免疫调节途径对HIV特异性CD4 + T细胞效应功能的影响

T cell exhaustion is a major factor in failed pathogen clearance during chronic viral infections. Immunoregulatory pathways, such as PD-1 and IL-10, are ...

Transplantation of Tail Skin to Study Allogeneic CD4 T Cell Responses in Mice

尾部皮肤来研究异基因CD4 + T细胞应答的小鼠移植

The study of T cell responses and their consequences during allo-antigen recognition requires a model that enables one to distinguish between donor and ...

Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice

Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice

诱导小鼠肠道炎症由效应CD4的过继转移<sup&gt; +</sup&gt; CD45RB<sup&gt;高</sup&gt; T细胞免疫缺陷小鼠

There are many different animal models available for studying the pathogenesis of human inflammatory bowel diseases (IBD), each with its own advantages ...

Mouse Na&#239;ve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

Mouse Na&#239;ve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

鼠标朴素CD4<sup&gt; +</sup&gt; T细胞分离和<em&gt;在体外</em&gt;分化为T细胞亚群

Antigen inexperienced (na&#239;ve) CD4+ T cells undergo expansion and differentiation to effector subsets at the time of T cell receptor (TCR) recognition ...