Woronicz J D, Calnan B, Ngo V, Winoto A
Department of Molecular and Cell Biology, University of California, Berkeley 94720.
Nature. 1994 Jan 20;367(6460):277-81. doi: 10.1038/367277a0.
Apoptosis is a phenomenon observed during development of many cell types in many organisms. It is an internal, programmed cell death characterized by DNA fragmentation into nucleosome-size pieces. Anti-CD3-induced apoptosis in T-cell hybridomas and immature thymocytes requires new gene transcription and may be related to negative selection during T-cell development. Using subtractive hybridization, we isolated a complementary DNA clone encoding the orphan steroid receptor Nur77 (refs 7-9). It shows different patterns of messenger RNA induction between apoptotic and stimulated T cells. We report here the use of gel shift analysis to demonstrate that the Nur77 protein is present at high levels in apoptotic T-cell hybridomas and apoptotic thymocytes, but not in growing T cells or stimulated splenocytes. A Nur77 dominant negative protected T-cell hybridomas from activation-induced apoptosis. Hence Nur77 is necessary for induced apoptosis in T-cell hybridomas.
细胞凋亡是在许多生物体中多种细胞类型发育过程中观察到的一种现象。它是一种由DNA断裂成核小体大小片段所表征的内部程序性细胞死亡。抗CD3诱导的T细胞杂交瘤和未成熟胸腺细胞凋亡需要新基因转录,并且可能与T细胞发育过程中的阴性选择有关。利用消减杂交技术,我们分离出了一个编码孤儿类固醇受体Nur77的互补DNA克隆(参考文献7 - 9)。它在凋亡T细胞和受刺激T细胞之间显示出不同的信使RNA诱导模式。我们在此报告使用凝胶迁移分析来证明Nur77蛋白在凋亡T细胞杂交瘤和凋亡胸腺细胞中高水平存在,但在生长中的T细胞或受刺激的脾细胞中不存在。一种Nur77显性阴性突变体保护T细胞杂交瘤免受激活诱导的凋亡。因此,Nur77是T细胞杂交瘤诱导凋亡所必需的。