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来自自身耐受型T细胞受体β链转基因小鼠的无反应性T细胞中抗原受体信号的改变。

Altered antigen receptor signaling in anergic T cells from self-tolerant T-cell receptor beta-chain transgenic mice.

作者信息

Blackman M A, Finkel T H, Kappler J, Cambier J, Marrack P

机构信息

Howard Hughes Medical Institute, Denver, CO.

出版信息

Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6682-6. doi: 10.1073/pnas.88.15.6682.

Abstract

T-cell tolerance to the minor lymphocyte-stimulating antigen Mls-1a in a T-cell receptor (TcR) V beta 8.1 transgenic line of mice is maintained by both clonal deletion and clonal anergy. Approximately 20-50% of peripheral CD4+ (but not CD8+) T cells isolated from these mice are anergic and fail to proliferate following TcR ligation. We have examined key events in T-cell signaling in peripheral T cells isolated from these mice. In this report, we show that the anergic CD4+ T cells did not mobilize calcium or express receptors for interleukin 2 (IL-2) following TcR ligation. However, the cells retained viability and functional potential because stimulation with phorbol 12-myristate 13-acetate and ionomycin bypassed the block in receptor-mediated signaling and induced IL-2 receptor expression and proliferation of the anergic cells.

摘要

在一个T细胞受体(TcR)Vβ8.1转基因小鼠品系中,T细胞对次要淋巴细胞刺激抗原Mls-1a的耐受性通过克隆清除和克隆无能来维持。从这些小鼠中分离出的外周CD4⁺(而非CD8⁺)T细胞中,约20% - 50%处于无能状态,在TcR连接后无法增殖。我们检测了从这些小鼠中分离出的外周T细胞中T细胞信号传导的关键事件。在本报告中,我们表明,无能的CD4⁺ T细胞在TcR连接后不会动员钙离子或表达白细胞介素2(IL-2)受体。然而,这些细胞保持了活力和功能潜力,因为用佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯和离子霉素刺激绕过了受体介导信号传导中的阻断,并诱导了无能细胞的IL-2受体表达和增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc9/52152/98a8c4224704/pnas01065-0306-a.jpg

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