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丝裂原活化蛋白激酶信号通路在造血调控中的作用

MAPK signaling pathways in the regulation of hematopoiesis.

作者信息

Geest Christian R, Coffer Paul J

机构信息

Department of Immunology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

J Leukoc Biol. 2009 Aug;86(2):237-50. doi: 10.1189/jlb.0209097. Epub 2009 Jun 4.

Abstract

The MAPKs are a family of serine/threonine kinases that play an essential role in connecting cell-surface receptors to changes in transcriptional programs. MAPKs are part of a three-component kinase module consisting of a MAPK, an upstream MEK, and a MEKK that couples the signals from cell-surface receptors to trigger downstream pathways. Three major groups of MAPKs have been characterized in mammals, including ERKs, JNKs, and p38MAPKs. Over the last decade, extensive work has established that these proteins play critical roles in the regulation of a wide variety of cellular processes including cell growth, migration, proliferation, differentiation, and survival. It has been demonstrated that ERK, JNK, and p38MAPK activity can be regulated in response to a plethora of hematopoietic cytokines and growth factors that play critical roles in hematopoiesis. In this review, we summarize the current understanding of MAPK function in the regulation of hematopoiesis in general and myelopoiesis in particular. In addition, the consequences of aberrant MAPK activation in the pathogenesis of various myeloid malignancies will be discussed.

摘要

丝裂原活化蛋白激酶(MAPKs)是一类丝氨酸/苏氨酸激酶家族,在将细胞表面受体与转录程序的变化联系起来方面发挥着重要作用。MAPKs是一个由MAPK、上游MEK和MEKK组成的三组分激酶模块的一部分,该模块将来自细胞表面受体的信号耦合起来以触发下游途径。在哺乳动物中已鉴定出三大类MAPKs,包括细胞外信号调节激酶(ERKs)、c-Jun氨基末端激酶(JNKs)和p38丝裂原活化蛋白激酶(p38MAPKs)。在过去十年中,大量研究表明这些蛋白质在调节包括细胞生长、迁移、增殖、分化和存活在内的多种细胞过程中发挥着关键作用。已经证明,ERK、JNK和p38MAPK的活性可响应于在造血过程中起关键作用的大量造血细胞因子和生长因子而受到调节。在本综述中,我们总结了目前对MAPK在一般造血调节特别是髓系造血调节中的功能的理解。此外,还将讨论异常MAPK激活在各种髓系恶性肿瘤发病机制中的后果。

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