Suppr超能文献

血小板生成素诱导的ERK激活对巨核细胞分化的需求以及p38对红系分化的需求。

Requirement of thrombopoietin-induced activation of ERK for megakaryocyte differentiation and of p38 for erythroid differentiation.

作者信息

Miyazaki R, Ogata H, Kobayashi Y

机构信息

Department of Pediatrics, Kansai Medical University, Osaka, Japan.

出版信息

Ann Hematol. 2001 May;80(5):284-91. doi: 10.1007/s002770000285.

Abstract

Thrombopoietin (TPO) plays a critical role not only in proliferation and differentiation of megakaryocytes but also in erythroid differentiation. We have investigated whether the different pathway of mitogen-activated protein kinase (MAPK) after TPO stimulation may discriminate megakaryocyte and erythroid differentiation. In this study, we have used human CD34+ hematopoietic progenitor cells (HPCs) from cord blood (CB) in serum-free liquid culture supplemented with TPO, to compare the respective effects of specific inhibitors of MAPK kinase (MEK) (PD98059) and p38 MAP kinase (p38) (SB203580) on megakaryocyte and erythroid development. PD98059, but not SB203580, significantly suppressed TPO-induced megakaryocyte differentiation when examined by the expression of CD41 and polyploidy assay. In the presence of SB203580, CD34+/CD36+ erythroid progenitors clearly decreased, whereas they increased when cultured with PD98059. These results indicate that activation of extracellular-signal-regulated kinase (ERK) is required for TPO-induced megakaryocyte differentiation and that p38 is required for TPO-induced erythroid differentiation.

摘要

血小板生成素(TPO)不仅在巨核细胞的增殖和分化中起关键作用,还在红系分化中起关键作用。我们研究了TPO刺激后丝裂原活化蛋白激酶(MAPK)的不同信号通路是否能区分巨核细胞和红系分化。在本研究中,我们使用来自脐带血(CB)的人CD34+造血祖细胞(HPCs),在添加TPO的无血清液体培养基中培养,以比较MAPK激酶(MEK)(PD98059)和p38 MAP激酶(p38)(SB203580)的特异性抑制剂对巨核细胞和红系发育的各自影响。当通过CD41表达和多倍体分析检测时,PD98059而非SB203580能显著抑制TPO诱导的巨核细胞分化。在存在SB203580的情况下,CD34+/CD36+红系祖细胞明显减少,而与PD98059一起培养时它们增加。这些结果表明,细胞外信号调节激酶(ERK)的激活是TPO诱导巨核细胞分化所必需的,而p38是TPO诱导红系分化所必需的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验