Seshadri T, Campisi J
Department of Biochemistry, Boston University Medical School, MA 02118.
Science. 1990 Jan 12;247(4939):205-9. doi: 10.1126/science.2104680.
Normal cells in culture invariably undergo senescence, whereby they cease proliferation after a finite number of doublings. Irreversible changes in gene expression occurred in senescent human fetal lung fibroblasts: a non-cell cycle-regulated mRNA was partially repressed; an unusual polyadenylated histone mRNA was expressed; although serum induced c-H-ras, c-myc, and ornithine decarboxylase mRNA normally, ornithine decarboxylase activity was deficient; and serum did not induce mRNA for a replication-dependent histone and for the c-fos proto-oncogene. The loss of c-fos inducibility was the result of a specific, transcriptional block. The results suggest that senescent fibroblasts were unable to proliferate because of, at least in part, selective repression of c-fos; moreover, the multiple changes in gene expression support the view that cellular senescence is a process of terminal differentiation.
培养中的正常细胞总是会经历衰老,即它们在有限次数的倍增后停止增殖。衰老的人胎儿肺成纤维细胞中发生了基因表达的不可逆变化:一种非细胞周期调控的mRNA被部分抑制;一种异常的多聚腺苷酸化组蛋白mRNA被表达;尽管血清通常会诱导c-H-ras、c-myc和鸟氨酸脱羧酶mRNA,但鸟氨酸脱羧酶活性不足;血清也不会诱导与复制相关的组蛋白和c-fos原癌基因的mRNA。c-fos诱导性的丧失是特定转录阻断的结果。这些结果表明,衰老的成纤维细胞至少部分由于c-fos的选择性抑制而无法增殖;此外,基因表达的多种变化支持了细胞衰老是一个终末分化过程的观点。