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在由温度敏感型SV40大T抗原基因永生化的细胞系中,p53的短暂增加会在非允许温度下诱导细胞凋亡。

Apoptosis is induced at nonpermissive temperature by a transient increase in p53 in cell lines immortalized with temperature-sensitive SV40 large T-antigen gene.

作者信息

Yanai N, Obinata M

机构信息

Department of Cell Biology, Tohoku University, Sendai, Japan.

出版信息

Exp Cell Res. 1994 Apr;211(2):296-300. doi: 10.1006/excr.1994.1090.

Abstract

Hepatocyte (TLR2) and kidney tubule (TKC2) cell lines established from temperature-sensitive (ts) SV40 T-antigen gene transgenic mice not only were arrested in growth, but also exhibited cell death at nonpermissive temperature (39 degrees C). The cell death was determined to be caused by apoptosis from observations of nuclear fragmentation and DNA fragmentation. These cell lines contained relatively high levels of wild-type p53 which formed complexes with T-antigen at permissive temperature (33 degrees C), but after shift to a nonpermissive temperature, the inactivation of T-antigens led to the liberation of an abundance of p53 proteins from the complexes, apparently inducing apoptosis.

摘要

从温度敏感(ts)的SV40 T抗原基因转基因小鼠建立的肝细胞系(TLR2)和肾小管细胞系(TKC2)不仅在生长上停滞,而且在非允许温度(39摄氏度)下表现出细胞死亡。通过观察核碎裂和DNA片段化确定细胞死亡是由凋亡引起的。这些细胞系含有相对高水平的野生型p53,其在允许温度(33摄氏度)下与T抗原形成复合物,但转移到非允许温度后,T抗原的失活导致大量p53蛋白从复合物中释放出来,显然诱导了凋亡。

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