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T细胞凋亡过程中失调的信使核糖核酸表达。

Deregulated messenger RNA expression during T cell apoptosis.

作者信息

Kerkhoff E, Ziff E B

机构信息

Howard Hughes Medical Institute, New York University Medical Center, Kaplan Cancer Center, Department of Biochemistry, NY 10016, USA.

出版信息

Nucleic Acids Res. 1995 Dec 11;23(23):4857-63. doi: 10.1093/nar/23.23.4857.

DOI:10.1093/nar/23.23.4857
PMID:8532529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC307475/
Abstract

The IL-2 dependent murine cytotoxic T cell line CTLL-2 undergoes programmed cell death when deprived of its specific cytokine. We analyzed the expression of cell cycle related genes after IL-2 deprivation. Here we show that a generalized decrease and re elevation of the levels of mRNA takes place as part of the apoptotic program. The levels of several mRNAs encoding cell cycle functions, including cyclin D2, cyclin D3, cyclin B1, c-myc and max all declined at 1.5-3 h following IL-2 deprivation. Notably, the maxmRNA, which was shown to be expressed in proliferating, growth arrested and differentiated cells, is down regulated with the same kinetics as the other mRNAs. Surprisingly, the mRNAs whose levels declined at 1.5-3 h rose again at 10-14 h, a time which closely followed the time of the first detection of apoptotic DNA degradation, at 8 h, but which precedes actual loss of viability, at 14 h, as measured by trypan blue exclusion. Of all analyzed genes only the expression of the S-phase specific histone H4 gene resists the initial decrease and declines gradually over the course of cell death. Measurement of c-Myc protein synthesis at a late stage of the apoptotic program revealed that the accumulated reinduced mRNA is not translated into protein. Because transcriptional regulation has been shown to be dependent on the chromatin structure, the reinduction may be triggered by relaxation of the chromatin caused by alterations in the chromatin structure of apoptotic cells.

摘要

依赖白细胞介素-2的小鼠细胞毒性T细胞系CTLL-2在缺乏其特异性细胞因子时会发生程序性细胞死亡。我们分析了白细胞介素-2剥夺后细胞周期相关基因的表达。在此我们表明,作为凋亡程序的一部分,mRNA水平会普遍下降然后再升高。几种编码细胞周期功能的mRNA水平,包括细胞周期蛋白D2、细胞周期蛋白D3、细胞周期蛋白B1、c-myc和max,在白细胞介素-2剥夺后1.5 - 3小时均下降。值得注意的是,已证实在增殖、生长停滞和分化细胞中表达的maxmRNA,其下调动力学与其他mRNA相同。令人惊讶的是,在1.5 - 3小时水平下降的mRNA在10 - 14小时再次上升,这个时间紧接在8小时首次检测到凋亡性DNA降解之后,但在14小时实际丧失活力之前(通过台盼蓝排斥法测定)。在所有分析的基因中,只有S期特异性组蛋白H4基因的表达抵抗最初的下降,并在细胞死亡过程中逐渐下降。在凋亡程序后期对c-Myc蛋白合成的测量表明,积累的重新诱导的mRNA没有翻译成蛋白质。由于转录调控已被证明依赖于染色质结构,这种重新诱导可能是由凋亡细胞染色质结构改变导致的染色质松弛所触发的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/ef62bb46a0fa/nar00023-0127-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/bf143d7450be/nar00023-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/707c4d043c52/nar00023-0127-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/ef62bb46a0fa/nar00023-0127-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/bf143d7450be/nar00023-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/707c4d043c52/nar00023-0127-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a1/307475/ef62bb46a0fa/nar00023-0127-b.jpg

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本文引用的文献

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