Massilamany Chandirasegaran, Gangaplara Arunakumar, Jia Ting, Elowsky Christian, Kang Guobin, Riethoven Jean-Jack, Li Qingsheng, Zhou You, Reddy Jay
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.
PLoS One. 2014 Jan 27;9(1):e87519. doi: 10.1371/journal.pone.0087519. eCollection 2014.
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.
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。