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促红细胞生成素诱导的J2E细胞分化和增殖刺激不能通过化学诱导模拟。

Erythropoietin-induced stimulation of differentiation and proliferation in J2E cells is not mimicked by chemical induction.

作者信息

Busfield S J, Klinken S P

机构信息

Department of Biochemistry, University of Western Australia, Nedlands.

出版信息

Blood. 1992 Jul 15;80(2):412-9.

PMID:1627799
Abstract

The J2E cell line is a novel erythroid cell line that differentiates in response to erythropoietin (Epo), the physiologic stimulus for erythropoiesis. After exposure to Epo, the cells synthesize hemoglobin, and we show here that this process is tightly linked to increases in cellular proliferation and DNA synthesis. The hormone-induced terminal differentiation also results in morphologic alterations and the accumulation of transcripts for alpha, beta maj, and beta min globins. c-myc messenger RNA levels increase rapidly after exposure to Epo and precede the increase in cell division, while c-myb undergoes a transient decrease. Differentiation of J2E cells can also be achieved with sodium butyrate, but, in contrast with Epo, this is associated with a retardation of replication and a sudden decrease in c-myc levels. These results show that, in this system, chemically induced differentiation differs from terminal maturation promoted by Epo and that the processes of proliferation and differentiation in J2E cells can be uncoupled.

摘要

J2E细胞系是一种新型的红细胞系,可响应促红细胞生成素(Epo)(红细胞生成的生理刺激因子)进行分化。暴露于Epo后,细胞合成血红蛋白,并且我们在此表明该过程与细胞增殖和DNA合成的增加紧密相关。激素诱导的终末分化还导致形态学改变以及α、βmaj和βmin珠蛋白转录本的积累。暴露于Epo后,c-myc信使RNA水平迅速增加,并先于细胞分裂的增加,而c-myb则经历短暂下降。用丁酸钠也可实现J2E细胞的分化,但与Epo相反,这与复制延迟和c-myc水平突然下降有关。这些结果表明,在该系统中,化学诱导的分化不同于Epo促进的终末成熟,并且J2E细胞中的增殖和分化过程可以解偶联。

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