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人类1号染色体在永生化细胞中诱导细胞衰老。

Induction of cellular senescence in immortalized cells by human chromosome 1.

作者信息

Sugawara O, Oshimura M, Koi M, Annab L A, Barrett J C

机构信息

National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709.

出版信息

Science. 1990 Feb 9;247(4943):707-10. doi: 10.1126/science.2300822.

Abstract

The control of cellular senescence by specific human chromosomes was examined in interspecies cell hybrids between diploid human fibroblasts and an immortal, Syrian hamster cell line. Most such hybrids exhibited a limited life span comparable to that of the human fibroblasts, indicating that cellular senescence is dominant in these hybrids. Karyotypic analyses of the hybrid clones that did not senesce revealed that all these clones had lost both copies of human chromosome 1, whereas all other human chromosomes were observed in at least some of the immortal hybrids. The application of selective pressure for retention of human chromosome 1 to the cell hybrids resulted in an increased percentage of hybrids that senesced. Further, the introduction of a single copy of human chromosome 1 to the hamster cells by microcell fusion caused typical signs of cellular senescence. Transfer of chromosome 11 had no effect on the growth of the cells. These findings indicate that human chromosome 1 may participate in the control of cellular senescence and further support a genetic basis for cellular senescence.

摘要

在二倍体人成纤维细胞与永生的叙利亚仓鼠细胞系之间的种间细胞杂种中,研究了特定人类染色体对细胞衰老的控制。大多数此类杂种表现出与人类成纤维细胞相当的有限寿命,这表明细胞衰老在这些杂种中占主导地位。对未衰老的杂种克隆进行的核型分析表明,所有这些克隆都丢失了人类染色体1的两个拷贝,而在至少一些永生杂种中观察到了所有其他人类染色体。对细胞杂种施加保留人类染色体1的选择压力导致衰老杂种的百分比增加。此外,通过微细胞融合将单拷贝的人类染色体1引入仓鼠细胞会导致细胞衰老的典型迹象。转移染色体11对细胞生长没有影响。这些发现表明人类染色体1可能参与细胞衰老的控制,并进一步支持细胞衰老的遗传基础。

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