MAPK signaling pathways in the regulation of hematopoiesis

被引:222
作者
Geest, Christian R. [1 ]
Coffer, Paul J. [1 ,2 ]
机构
[1] Univ Med Ctr Utrecht, Dept Immunol, Mol Immunol Lab, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Pediat Immunol, NL-3584 CX Utrecht, Netherlands
关键词
CD34+; signal transduction; transcription; ERK; p38; JNK; ACTIVATED PROTEIN-KINASE; ACUTE MYELOID-LEUKEMIA; N-TERMINAL KINASE; GROWTH-FACTOR RECEPTOR; INDUCED ERYTHROID-DIFFERENTIATION; TRANSCRIPTION FACTOR; P38; MAPK; C/EBP-ALPHA; CELL-CYCLE; MEGAKARYOCYTIC DIFFERENTIATION;
D O I
10.1189/jlb.0209097
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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. J. Leukoc. Biol. 86: 237-250; 2009.
引用
收藏
页码:237 / 250
页数:14
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