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人染色体6在端粒酶阴性的人永生化成纤维细胞系LCS-AF.1-3中诱导细胞衰老。

Induction of cellular senescence in a telomerase negative human immortal fibroblast cell line, LCS-AF.1-3, by human chromosome 6.

作者信息

Kumata M, Shimizu M, Oshimura M, Uchida M, Tsutsui T

机构信息

Oral and Maxillofacial Surgery, The Nippon Dental University Hospital at Tokyo, Tokyo 102-8158, Japan.

出版信息

Int J Oncol. 2002 Oct;21(4):851-6. doi: 10.3892/ijo.21.4.851.

Abstract

In immortal cells (LCS-AF.1-3) which originated from cultured skin fibroblasts from a patient with Li-Fraumeni syndrome, a specific deletion has been identified on chromosome 6. To examine the relationship between this deletion and the loss of function in aging genes, we performed microcell mediated chromosome transfer (MMCT) of normal human chromosome 6 into LCS-AF.1-3 cells and analyzed their characteristics. Transferred human chromosome 6 induced morphological changes in the cells and cellular senescence with growth suppression. In a revertant clone that had escaped from induced senescence, a specific deletion was found at D6S309 in the transferred chromosome 6. High molecular weight telomeric sequences were lost in a clone that had been induced to senescence by introduction of human chromosome 6. On the other hand, human chromosome 7 induces senescence in immortal cells by suppressing the alternative lengthening of telomere (ALT) mechanism. We also performed MMCT of chromosome 7 and discuss the effect of chromosome transfer by comparing the two chromosomes. LCS-AF.1-3 cells containing a transferred chromosome 7 showed no changes in immortality. These results suggest that genes which are new candidates for aging and which suppress the ALT mechanism are located in the region D6S309 in human chromosome 6.

摘要

在源自一名李-弗劳梅尼综合征患者培养皮肤成纤维细胞的永生细胞(LCS-AF.1-3)中,已在6号染色体上鉴定出一个特定缺失。为了研究这种缺失与衰老基因功能丧失之间的关系,我们将正常人6号染色体通过微细胞介导的染色体转移(MMCT)导入LCS-AF.1-3细胞,并分析了它们的特性。转移的人6号染色体诱导细胞形态发生变化并导致细胞衰老及生长抑制。在一个逃脱诱导衰老的回复克隆中,发现转移的6号染色体上的D6S309处存在特定缺失。通过导入人6号染色体诱导衰老的一个克隆中,高分子量端粒序列丢失。另一方面,人7号染色体通过抑制端粒替代延长(ALT)机制诱导永生细胞衰老。我们还进行了7号染色体的MMCT,并通过比较这两条染色体来讨论染色体转移的效果。含有转移7号染色体的LCS-AF.1-3细胞在永生性方面没有变化。这些结果表明,作为衰老新候选基因且抑制ALT机制的基因位于人6号染色体的D6S309区域。

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