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使用主要组织相容性复合体II类右旋糖酐聚合物进行直接染色可在原位检测抗原特异性自身反应性CD4 T细胞。

Direct staining with major histocompatibility complex class II dextramers permits detection of antigen-specific, autoreactive CD4 T cells in situ.

作者信息

Massilamany Chandirasegaran, Gangaplara Arunakumar, Jia Ting, Elowsky Christian, Kang Guobin, Riethoven Jean-Jack, Li Qingsheng, Zhou You, Reddy Jay

机构信息

School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, United States of America.

Center for Biotechnology, University of Nebraska-Lincoln, Lincoln, Nebraska, United States of America.

出版信息

PLoS One. 2014 Jan 27;9(1):e87519. doi: 10.1371/journal.pone.0087519. eCollection 2014.

Abstract

We report here the utility of major histocompatibility complex (MHC) class II dextramers for in situ detection of self-reactive CD4 T cells in two target organs, the brain and heart. We optimized the conditions for in situ detection of antigen-specific CD4 T cells using brain sections obtained from SJL mice immunized with myelin proteolipid protein (PLP) 139-151; the sections were costained with IA(s)/PLP 139-151 (specific) or Theiler's murine encephalomyelitis virus (TMEV) 70-86 (control) dextramers and anti-CD4. Analysis of sections by laser scanning confocal microscope revealed detection of cells positive for PLP 139-151 but not for TMEV 70-86 dextramers to be colocalized with CD4-expressing T cells, indicating that the staining was specific to PLP 139-151 dextramers. Further, we devised a method to reliably enumerate the frequencies of antigen-specific T cells by counting the number of dextramer⁺ CD4⁺ T cells in the 'Z' serial images acquired sequentially. We next extended these observations to detect cardiac myosin-specific T cells in autoimmune myocarditis induced in A/J mice by immunizing with cardiac myosin heavy chain-α (Myhc) 334-352. Heart sections prepared from immunized mice were costained with Myhc 334-352 (specific) or bovine ribonuclease 43-56 (control) dextramers together with anti-CD4; the sections showed the infiltrations of Myhc-specific CD4 T cells. The data suggest that MHC class II dextramers are useful tools for enumerating the frequencies of antigen-specific CD4 T cells in situ by direct staining without having to amplify the fluorescent signals, an approach commonly employed with conventional MHC tetramers.

摘要

我们在此报告主要组织相容性复合体(MHC)II类右旋糖酐聚合物在原位检测脑和心脏这两个靶器官中自身反应性CD4 T细胞的效用。我们利用从用髓鞘蛋白脂蛋白(PLP)139 - 151免疫的SJL小鼠获得的脑切片,优化了原位检测抗原特异性CD4 T细胞的条件;这些切片用IA(s)/PLP 139 - 151(特异性)或泰勒氏鼠脑脊髓炎病毒(TMEV)70 - 86(对照)右旋糖酐聚合物和抗CD4进行复染色。通过激光扫描共聚焦显微镜对切片进行分析,结果显示检测到PLP 139 - 151阳性但TMEV 70 - 86右旋糖酐聚合物阴性的细胞与表达CD4的T细胞共定位,这表明该染色对PLP 139 - 151右旋糖酐聚合物具有特异性。此外,我们设计了一种方法,通过依次计数在连续获取的“Z”系列图像中右旋糖酐聚合物⁺CD4⁺T细胞的数量,可靠地计算抗原特异性T细胞的频率。接下来,我们将这些观察结果扩展到检测在A/J小鼠中通过用心肌肌球蛋白重链-α(Myhc)334 - 352免疫诱导的自身免疫性心肌炎中的心肌肌球蛋白特异性T细胞。从免疫小鼠制备的心脏切片用Myhc 334 - 352(特异性)或牛核糖核酸酶43 - 56(对照)右旋糖酐聚合物与抗CD4一起进行复染色;切片显示了Myhc特异性CD4 T细胞的浸润。数据表明,MHC II类右旋糖酐聚合物是用于通过直接染色原位计算抗原特异性CD4 T细胞频率的有用工具,而无需放大荧光信号,这是传统MHC四聚体常用的方法。

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