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弗瑞德红白血病细胞分化过程中p53合成的减少。与终末细胞分裂的关联。

Reduction in p53 synthesis during differentiation of Friend-erythroleukemia cells. Correlation with the commitment to terminal cell division.

作者信息

Ben-Dori R, Resnitzki D, Kimchi A

出版信息

FEBS Lett. 1983 Oct 17;162(2):384-9. doi: 10.1016/0014-5793(83)80792-3.

Abstract

The process of cell differentiation in Friend-erythroleukemia cells was accompanied by 80-90% inhibition of p53 synthesis. This decrease was found to be linked to changes in cell-cycle distribution characteristics of the growth arrest program during differentiation rather than to the induction of the globin genes. The shut-off in the expression of p53 always preceded the specific arrest of cells in the G0/G1 phase. Interferon did not modulate down the expression of p53 if added to transformed non-induced Friend-erythroleukemia cells; however, it slightly enhanced the extent of reduction in p53 synthesis if added during cell differentiation, thus suggesting a differential effect of interferon between cells at different stages of differentiation.

摘要

在弗瑞德-埃里氏白血病细胞中,细胞分化过程伴随着p53合成受到80%-90%的抑制。研究发现,这种减少与分化过程中生长停滞程序的细胞周期分布特征变化有关,而非与珠蛋白基因的诱导有关。p53表达的关闭总是先于细胞在G0/G1期的特异性停滞。如果将干扰素添加到转化的未诱导弗瑞德-埃里氏白血病细胞中,它不会下调p53的表达;然而,如果在细胞分化过程中添加,它会略微增强p53合成的减少程度,这表明干扰素在细胞分化的不同阶段对细胞有不同的作用。

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