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MKP-2:走出 DUSP 家族,重回聚光灯下。

MKP-2: out of the DUSP-bin and back into the limelight.

机构信息

Division of Cell Biology, University of Strathclyde, Strathclyde Institute of Pharmacy and Biomedical Sciences, 161 Cathedral Street, Glasgow G4 0RE, UK.

出版信息

Biochem Soc Trans. 2012 Feb;40(1):235-9. doi: 10.1042/BST20110648.

Abstract

The MKPs (mitogen-activated protein kinase phosphatases) are a family of at least ten DUSPs (dual-specificity phosphatases) which function to terminate the activity of the MAPKs (mitogen-activated protein kinases). Several members have already been demonstrated to have distinct roles in immune function, cancer, fetal development and metabolic disorders. One DUSP of renewed interest is the inducible nuclear phosphatase MKP-2, which dephosphorylates both ERK (extracellular-signal-regulated kinase) and JNK (c-Jun N-terminal kinase) in vitro. Recently, the understanding of MKP-2 function has been advanced due to the development of mouse knockout models, which has resulted in the discovery of novel roles for MKP-2 in the regulation of sepsis, infection and cell-cycle progression that are distinct from those of other DUSPs. However, many functions for MKP-2 still await to be characterized.

摘要

MKP 蛋白(丝裂原活化蛋白激酶磷酸酶)是一个至少包含十个双特异性磷酸酶(DUSP)的家族,其功能是终止 MAPK(丝裂原活化蛋白激酶)的活性。已经有几个成员被证明在免疫功能、癌症、胎儿发育和代谢紊乱中具有不同的作用。重新引起关注的 DUSP 之一是诱导性核磷酸酶 MKP-2,它在体外使 ERK(细胞外信号调节激酶)和 JNK(c-Jun N-末端激酶)去磷酸化。最近,由于开发了小鼠敲除模型,对 MKP-2 功能的理解得到了推进,这导致发现了 MKP-2 在调节败血症、感染和细胞周期进展中的新作用,这些作用与其他 DUSP 不同。然而,MKP-2 的许多功能仍有待进一步研究。

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