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促红细胞生成素和干细胞因子对丝裂原活化蛋白激酶(ERK1/2)的协同激活作用对于增强红细胞生成至关重要。

Synergistic activation of MAP kinase (ERK1/2) by erythropoietin and stem cell factor is essential for expanded erythropoiesis.

作者信息

Sui X, Krantz S B, You M, Zhao Z

机构信息

Hematology Division, Department of Medicine, Department of Veterans Affairs Medical Center, and Vanderbilt Cancer Center, Vanderbilt University, Nashville, TN 37232-6305, USA.

出版信息

Blood. 1998 Aug 15;92(4):1142-9.

PMID:9694701
Abstract

Stem cell factor (SCF) and erythropoietin (EPO) work synergistically to support erythropoiesis, but the mechanism for this synergism is unknown. By using purified human erythroid colony-forming cells (ECFC), we have found that SCF and EPO synergistically activate MAP kinase (MAPK, ERK1/2), which correlates with the cell growth and thus may be responsible for the synergistic effects. Treatment of the cells with PD98059 and wortmannin, inhibitors of MEK and PI-3 kinase, respectively, inhibited the synergistic activation of MAPK and also the cell growth, further supporting this conclusion. Wortmannin only inhibits MAPK activation induced by EPO but not that by SCF, suggesting that SCF and EPO may activate MAPK through different pathways, which would facilitate synergy. Furthermore, EPO, but not SCF, led to activation of STAT5, whereas SCF and wortmannin had no effect on the EPO-induced STAT5 activation, suggesting that STAT5 is not involved in the synergistic action of SCF and EPO. Together, the data suggest that synergistic activation of MAPK by SCF and EPO is essential for expanded erythropoiesis.

摘要

干细胞因子(SCF)和促红细胞生成素(EPO)协同作用以支持红细胞生成,但其协同作用机制尚不清楚。通过使用纯化的人红系集落形成细胞(ECFC),我们发现SCF和EPO协同激活丝裂原活化蛋白激酶(MAPK,ERK1/2),这与细胞生长相关,因此可能是协同效应的原因。分别用MEK和PI-3激酶抑制剂PD98059和渥曼青霉素处理细胞,抑制了MAPK的协同激活以及细胞生长,进一步支持了这一结论。渥曼青霉素仅抑制EPO诱导的MAPK激活,而不抑制SCF诱导的MAPK激活,这表明SCF和EPO可能通过不同途径激活MAPK,这将促进协同作用。此外,EPO而非SCF导致STAT5激活,而SCF和渥曼青霉素对EPO诱导的STAT5激活没有影响,这表明STAT5不参与SCF和EPO的协同作用。总之,数据表明SCF和EPO对MAPK的协同激活对于红细胞生成的扩增至关重要。

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