首页> 外文期刊>Experimental Gerontology >mRNA levels of the differentiation-associated linker histone variant H1 zero in mitotically active and postmitotic senescent human diploid fibroblast cell populations.
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mRNA levels of the differentiation-associated linker histone variant H1 zero in mitotically active and postmitotic senescent human diploid fibroblast cell populations.

机译:在有丝分裂活跃和有丝分裂后衰老的人类二倍体成纤维细胞群中,分化相关的接头组蛋白变体H1的mRNA水平为零。

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The mRNA levels of the linker histone variant H1o, which is tightly associated with differentiation, have been studied in the present investigation in an in vitro model ageing human diploid fibroblast (HDF) cell system as a function of cumulative population doublings (CPDs) in mitotically active and senescent cell populations. According to our previous findings the synthesis rate of the H1o protein does not change as a function of CPDs as long as the cells are proliferating. However, when cells reach senescence, the synthesis rate of H1o increases in both naturally aged as well as in cell populations artificially aged by treatment with sodium butyrate. In the present investigation, it is shown that the H1o mRNA levels remain relatively constant in mitotic cells with a slight decrease in cell cultures of late CPDs, i.e. in populations which still retain a mitotic potential, but are toward the end of their proliferative lifespan. However, when cells senesce and are no longer capable of synthesizing DNA, the H1o mRNA levels increase in naturally aged cells while artificially aged cells still maintain mRNA levels comparable to those of mitotic cells.
机译:与分化密切相关的接头组蛋白变体H1o的mRNA水平在本研究中已在体外模型衰老的人类二倍体成纤维细胞(HDF)细胞系统中作为有丝分裂中累积种群倍增(CPD)的函数进行了研究活跃和衰老的细胞群。根据我们先前的发现,只要细胞正在增殖,H10蛋白的合成速率就不会随CPD的变化而改变。但是,当细胞达到衰老时,在自然衰老以及通过丁酸钠处理人工衰老的细胞群体中,H10的合成速率都会增加。在本研究中,显示出有丝分裂细胞中H10 mRNA水平保持相对恒定,而后期CPD的细胞培养物即仍保留有丝分裂潜能但接近其增殖寿命的群体中H1mRNA水平略有下降。但是,当细胞衰老并且不再能够合成DNA时,自然衰老细胞中的H1mRNA水平会增加,而人工衰老细胞仍保持与有丝分裂细胞相当的mRNA水平。

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