Suppr超能文献

幼稚T细胞存活对钙调神经磷酸酶aβ的需求。

Requirement of calcineurin a beta for the survival of naive T cells.

作者信息

Manicassamy Santhakumar, Gupta Sonal, Huang Zhaofeng, Molkentin Jeffery D, Shang Weirong, Sun Zuoming

机构信息

Division of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.

出版信息

J Immunol. 2008 Jan 1;180(1):106-12. doi: 10.4049/jimmunol.180.1.106.

Abstract

Calcineurin (Cn) is a Ca2+/calmodulin-dependent phosphatase that dephosphorylates and activates NFAT, a transcription factor essential for T cell activation. T lymphocytes predominantly express the calcineurin Abeta (CnAbeta) isoform, and the deletion of the CnAbeta gene results in defective T cell proliferation and IL-2 production in response to TCR stimulation. In this study, we show that CnAbeta enhances the spontaneous survival of naive T cells by maintaining high levels of Bcl-2, a critical homeostatic survival factor for naive T cells. T cells obtained from CnAbeta-/- mice displayed accelerated spontaneous apoptosis. The observed apoptosis of the CnAbeta-/- T cells was prevented by IL-7 and IL-15, two cytokines critical for the homeostatic survival of naive T cells. Furthermore, CD4+ or CD8+ single positive CnAbeta-/- thymocytes also underwent accelerated apoptosis. However, no obvious difference in the apoptosis of CD4+CD8+ double positive thymocytes was observed between CnAbeta-/- and wild-type mice, suggesting a specific function of CnAbeta in the survival of single positive T cells. Bcl-2 levels were found to be significantly lower in CnAbeta-/- T cells. Transgenic expression of Bcl-xL restored the survival of the CnAbeta-/- T cells. Thus, in addition to its role in mediating TCR signals essential for T cell activation, CnAbeta is also required for the homeostatic survival of naive T cells.

摘要

钙调神经磷酸酶(Cn)是一种Ca2+/钙调蛋白依赖性磷酸酶,可使活化T细胞核因子(NFAT)去磷酸化并激活该因子,NFAT是T细胞活化所必需的转录因子。T淋巴细胞主要表达钙调神经磷酸酶Aβ(CnAβ)亚型,CnAβ基因的缺失会导致T细胞在受到TCR刺激时增殖缺陷和白细胞介素-2生成减少。在本研究中,我们发现CnAβ通过维持高水平的Bcl-2(一种对初始T细胞至关重要的稳态存活因子)来增强初始T细胞的自发存活能力。从CnAβ基因敲除小鼠获得的T细胞表现出加速的自发凋亡。白细胞介素-7和白细胞介素-15(对初始T细胞的稳态存活至关重要的两种细胞因子)可防止观察到的CnAβ基因敲除T细胞的凋亡。此外,CD4+或CD8+单阳性的CnAβ基因敲除胸腺细胞也经历了加速凋亡。然而,在CnAβ基因敲除小鼠和野生型小鼠之间,未观察到CD4+CD8+双阳性胸腺细胞凋亡的明显差异,这表明CnAβ在单阳性T细胞存活中具有特定功能。发现CnAβ基因敲除T细胞中的Bcl-2水平显著降低。Bcl-xL的转基因表达恢复了CnAβ基因敲除T细胞的存活能力。因此,除了其在介导T细胞活化所必需的TCR信号方面的作用外,CnAβ也是初始T细胞稳态存活所必需的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验