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CD3复合物刺激后NOD小鼠T淋巴细胞上Ly-6C的表达。糖尿病前期小鼠胰岛炎期间活化细胞的鉴定。

Expression of Ly-6C by T lymphocytes of NOD mice after CD3-complex stimulation. Identification of activated cells during insulitis of prediabetic mice.

作者信息

Herold K C, Montag A G, Meyer S M, Wojcikowski C, Fitch F W

机构信息

Department of Medicine and Pathology, University of Chicago, Pritzker School of Medicine, Illinois 60637.

出版信息

Diabetes. 1990 Jul;39(7):815-20. doi: 10.2337/diab.39.7.815.

Abstract

Ly-6C is a differentiation antigen that distinguishes T-lymphocyte subsets. In concordance with previous results, splenocytes from NOD mice do not express the epitope recognized by anti-Ly-6C monoclonal antibodies (MoAbs), including MoAb HK1.4 in this study, and cannot be stimulated to proliferate in response to HK1.4. However, when splenocytes from NOD mice were stimulated in vitro with the anti-CD3 MoAb 145-2C11, T lymphocytes expressing Ly-6C were detected after 48 h of stimulation, with as many as 25% of lymphocytes expressing this antigen with prolonged passage in culture. Most of the cells expressing Ly-6C were Thy-1.2+, CD4+, and CD8- and proliferated after stimulation with HK1.4. To further understand the failure of NOD splenocytes to express Ly-6C, freshly isolated cells were stimulated with alpha/beta-interferon (IFN-alpha/beta) and IFN-gamma. Although these lymphokines induced expression of Ly-6A and Ly-6C in splenocytes from C57BL/6J mice and Ly-6A in NOD cells, Ly-6C was not induced on NOD cells. Because Ly-6C expression on splenocytes was a marker of activation via the CD3 T-lymphocyte receptor complex, we also examined expression of Ly-6C on T lymphocytes within islets showing insulitis in vivo. Lymphocytes that were Ly-6C+ were identified within islets on histological sections of pancreas, whereas Ly-6C+ cells in the spleen from the same mouse could not be detected. Our findings imply functional abnormality in expression of Ly-6C in NOD mice.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

Ly-6C是一种区分T淋巴细胞亚群的分化抗原。与先前的结果一致,NOD小鼠的脾细胞不表达抗Ly-6C单克隆抗体(MoAb)识别的表位,包括本研究中的MoAb HK1.4,并且不能被刺激以响应HK1.4而增殖。然而,当用抗CD3 MoAb 145-2C11体外刺激NOD小鼠的脾细胞时,刺激48小时后检测到表达Ly-6C的T淋巴细胞,随着培养传代时间延长,多达25%的淋巴细胞表达该抗原。大多数表达Ly-6C的细胞是Thy-1.2+、CD4+和CD8-,并且在用HK1.4刺激后增殖。为了进一步了解NOD脾细胞不表达Ly-6C的原因,用α/β干扰素(IFN-α/β)和IFN-γ刺激新鲜分离的细胞。尽管这些淋巴因子在C57BL/6J小鼠的脾细胞中诱导Ly-6A和Ly-6C的表达,在NOD细胞中诱导Ly-6A的表达,但在NOD细胞上未诱导Ly-6C的表达。由于脾细胞上Ly-6C的表达是通过CD3 T淋巴细胞受体复合物激活的标志物,我们还检查了体内显示胰岛炎的胰岛内T淋巴细胞上Ly-6C的表达。在胰腺组织切片的胰岛内鉴定出Ly-6C+的淋巴细胞,而在同一只小鼠脾脏中未检测到Ly-6C+细胞。我们的发现暗示NOD小鼠中Ly-6C表达存在功能异常。(摘要截短至250字)

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