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细胞毒性T淋巴细胞相关抗原4(CTLA-4)在体内调节无反应性的诱导。

CTLA-4 regulates induction of anergy in vivo.

作者信息

Greenwald R J, Boussiotis V A, Lorsbach R B, Abbas A K, Sharpe A H

机构信息

Immunology Research Division, Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Immunity. 2001 Feb;14(2):145-55. doi: 10.1016/s1074-7613(01)00097-8.

Abstract

The requirement for CTLA-4 during the induction of peripheral T cell tolerance in vivo was investigated using naive TCR transgenic T cells lacking CTLA-4. CTLA-4(-/-) T cells are resistant to tolerance induction, as demonstrated by their proliferative responses, IL-2 production, and progression into the cell cycle. Following exposure to a tolerogenic stimulus in vivo and restimulation in vitro, wild-type T cells are blocked at the late G1 to S restriction point of the cell cycle. In contrast, CTLA-4(-/-) T cells enter into the S phase of the cell cycle, as shown by downregulation of p27(kip1), elevated cdk2 kinase activity, and Rb hyperphosphorylation. Thus, CTLA-4 has an essential role in determining the outcome of T cell encounter with a tolerogenic stimulus.

摘要

利用缺乏CTLA-4的初始TCR转基因T细胞,研究了体内外周T细胞耐受性诱导过程中对CTLA-4的需求。CTLA-4(-/-) T细胞对耐受性诱导具有抗性,这通过它们的增殖反应、IL-2产生以及进入细胞周期得以证明。在体内暴露于致耐受性刺激并在体外再次刺激后,野生型T细胞在细胞周期的G1晚期至S限制点被阻断。相比之下,CTLA-4(-/-) T细胞进入细胞周期的S期,这表现为p27(kip1)下调、cdk2激酶活性升高以及Rb过度磷酸化。因此,CTLA-4在决定T细胞与致耐受性刺激相遇的结果中起关键作用。

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