Oukka M, Ho I C, de la Brousse F C, Hoey T, Grusby M J, Glimcher L H
Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Immunity. 1998 Sep;9(3):295-304. doi: 10.1016/s1074-7613(00)80612-3.
Nuclear factor of activated T cells (NFAT) is a family of four related transcription factors implicated in cytokine and early response gene expression in activated lymphocytes. Here we report that NFAT4, in contrast to NFATp and NFATc, is preferentially expressed in DP thymocytes. Mice lacking NFAT4 have impaired development of CD4 and CD8 SP thymocytes and peripheral T cells as well as hyperactivation of peripheral T cells. The thymic defect is characterized by increased apoptosis of DP thymocytes. The increased apoptosis and hyperactivation may reflect heightened sensitivity to TcR-mediated signaling. Further, mice lacking NFAT4 have impaired production of Bcl-2 mRNA and protein. NFAT4 thus plays an important role in the successful generation and survival of T cells.
活化T细胞核因子(NFAT)是一个由四个相关转录因子组成的家族,参与活化淋巴细胞中细胞因子和早期反应基因的表达。我们在此报告,与NFATp和NFATc不同,NFAT4在双阳性(DP)胸腺细胞中优先表达。缺乏NFAT4的小鼠,其CD4和CD8单阳性(SP)胸腺细胞以及外周T细胞的发育受损,同时外周T细胞过度活化。胸腺缺陷的特征是DP胸腺细胞凋亡增加。凋亡增加和过度活化可能反映了对T细胞受体(TcR)介导信号的敏感性增强。此外,缺乏NFAT4的小鼠Bcl-2 mRNA和蛋白的产生受损。因此,NFAT4在T细胞的成功生成和存活中发挥重要作用。