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SV40 T抗原诱导的细胞凋亡与c-jun的过表达相关。

The induction of apoptosis by SV40 T antigen correlates with c-jun overexpression.

作者信息

Chen S L, Tsao Y P, Chen Y L, Huang S J, Chang J L, Wu S F

机构信息

Department of Microbiology and Immunology, Graduate Institute of Medical Science, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

Virology. 1998 May 10;244(2):521-9. doi: 10.1006/viro.1998.9109.

Abstract

Simian virus (SV40) T antigen shares many characteristics with adenovirus E1A which is known to induce apoptosis. To verify the potential of SV40 T antigen-mediated apoptosis, we stably expressed T antigen in immortalized human epithelial cells (Z172 and HaCaT). We found that SV40 T antigen could directly cause apoptosis in 22-27% of these cells under normal growth condition as measured by chromatin condensation and nucleosomal fragmentation. The apoptosis of HaCaT cells which contain mutant p53 suggests the p53-independent nature of T antigen-mediated apoptosis. T antigen-induced apoptosis was associated with increased expression of c-Jun protein. Moreover, the overexpression of c-jun alone in these cells also induced apoptosis, indicating that c-jun might play an important role in T antigen-induced apoptosis.

摘要

猿猴病毒(SV40)T抗原与已知可诱导细胞凋亡的腺病毒E1A具有许多共同特征。为了验证SV40 T抗原介导细胞凋亡的可能性,我们在永生化人上皮细胞(Z172和HaCaT)中稳定表达了T抗原。我们发现,通过染色质浓缩和核小体片段化检测,在正常生长条件下,SV40 T抗原可直接导致22%至27%的这些细胞发生凋亡。含有突变型p53的HaCaT细胞发生凋亡,提示T抗原介导的细胞凋亡不依赖p53。T抗原诱导的细胞凋亡与c-Jun蛋白表达增加有关。此外,在这些细胞中单独过表达c-jun也可诱导细胞凋亡,表明c-jun可能在T抗原诱导的细胞凋亡中起重要作用。

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