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雷帕霉素抑制J2E细胞增殖但不抑制其红系分化。

Inhibition of proliferation but not erythroid differentiation of J2E cells by rapamycin.

作者信息

Jaster R, Bittorf T, Klinken S P, Brock J

机构信息

Institute of Medical Biochemistry, Medical Faculty of the University of Rostock, Germany.

出版信息

Biochem Pharmacol. 1996 May 3;51(9):1181-5. doi: 10.1016/0006-2952(96)00044-5.

Abstract

During erythropoiesis, replication and maturation are tightly coupled processes. Here, we show that the immunosuppressant rapamycin inhibited basal- as well as erythropoietin-stimulated proliferation of the erythroid cell line J2E. In addition, it enhanced the antiproliferative effect of sodium butyrate. Although rapamycin suppressed erythroid cell division, it did not affect terminal differentiation induced by erythropoietin or sodium butyrate. The proliferative status of J2E cells correlated well with the activity of the ribosomal S6 kinase p70S6k, an enzyme effectively blocked by rapamycin. It was concluded from this study that erythroid maturation proceeded normally despite the rapamycin-induced inhibition of mitosis and of p70S6k activity. These data provide further evidence that separate signalling pathways for proliferation and differentiation exist in erythroid cells.

摘要

在红细胞生成过程中,复制和成熟是紧密耦合的过程。在此,我们表明免疫抑制剂雷帕霉素可抑制红系细胞系J2E的基础增殖以及促红细胞生成素刺激的增殖。此外,它增强了丁酸钠的抗增殖作用。虽然雷帕霉素抑制红系细胞分裂,但它不影响促红细胞生成素或丁酸钠诱导的终末分化。J2E细胞的增殖状态与核糖体S6激酶p70S6k的活性密切相关,该酶可被雷帕霉素有效阻断。从这项研究得出的结论是,尽管雷帕霉素诱导有丝分裂和p70S6k活性受到抑制,但红系成熟仍正常进行。这些数据进一步证明红系细胞中存在增殖和分化的独立信号通路。

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