Wu Chia-Cheng, Hsu Shu-Ching, Shih Hsiu-Ming, Lai Ming-Zong
Graduate Institute of Immunology, School of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China.
Mol Cell Biol. 2003 Sep;23(18):6442-54. doi: 10.1128/MCB.23.18.6442-6454.2003.
p38 mitogen activated protein kinase (MAPK) is essential for T-cell activation. Here we demonstrated that nuclear factor of activated T cells (NFAT) is a direct target of p38 MAPK. Inhibition of p38 MAPK led to selective inactivation of NFAT in T cells. We further linked a strict requirement of p38 MAPK to activation of NFATc. A stimulatory effect of p38 MAPK on at least four other stages of NFATc activation was found. First, the p38 MAPK cascade activated the NFATc promoter and induced the transcription of NFATc mRNA. Second, p38 MAPK mildly increased the mRNA stability of NFATc. Third, p38 MAPK enhanced the translation of NFATc mRNA. Fourth, p38 MAPK promoted the interaction of NFATc with the coactivator CREB-binding protein. In contrast, p38 MAPK moderately enhanced the expulsion of NFATc from the nucleus in T cells. Therefore, p38 MAPK has opposite effects on different stages of NFATc activation. All together, the overall effect of p38 MAPK on NFATc in T cells is clear activation.
p38丝裂原活化蛋白激酶(MAPK)对于T细胞活化至关重要。在此我们证明活化T细胞核因子(NFAT)是p38 MAPK的直接靶点。抑制p38 MAPK会导致T细胞中NFAT选择性失活。我们进一步将p38 MAPK的严格需求与NFATc的活化联系起来。发现p38 MAPK对NFATc活化的至少其他四个阶段具有刺激作用。首先,p38 MAPK级联反应激活NFATc启动子并诱导NFATc mRNA的转录。其次,p38 MAPK轻度增加NFATc的mRNA稳定性。第三,p38 MAPK增强NFATc mRNA的翻译。第四,p38 MAPK促进NFATc与共激活因子CREB结合蛋白的相互作用。相反,p38 MAPK适度增强T细胞中NFATc从细胞核的排出。因此,p38 MAPK对NFATc活化的不同阶段具有相反的作用。总体而言,p38 MAPK对T细胞中NFATc的总体作用是明显的激活。