Manicassamy Santhakumar, Gupta Sonal, Huang Zhaofeng, Molkentin Jeffery D, Shang Weirong, Sun Zuoming
Division of Immunology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.
J Immunol. 2008 Jan 1;180(1):106-12. doi: 10.4049/jimmunol.180.1.106.
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.
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。