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丝裂原活化蛋白激酶激酶4(MKK4)。

Mitogen-activated protein kinase kinase 4 (MKK4).

作者信息

Cuenda A

机构信息

Medical Research Council Protein Phosphorylation Unit, Department of Biochemistry, University of Dundee, MSI/WTB Complex, Dundee, UK.

出版信息

Int J Biochem Cell Biol. 2000 Jun;32(6):581-7. doi: 10.1016/s1357-2725(00)00003-0.

Abstract

The Mitogen-Activated Protein Kinase Kinase 4 (MKK4), a member of the MAP kinase kinase family, directly phosphorylates and activates the c-Jun NH2-terminal kinases (JNK), in response to cellular stresses and proinflammatory cytokines. JNK is a member of the MAP kinase family and a key component of a stress activated protein kinase signalling pathway. MKK4 mRNA is widely expressed in adult mouse tissues, but is especially abundant in skeletal muscle and brain. Mice lacking the MKK4 gene had abnormal hepatogenesis and died before embryonic day 14. However cell lines lacking MKK4 have been obtained and these exhibited defective activation of JNK and AP-1 dependent transcription activity in response to some, but not all cellular stresses. Furthermore, T lymphocytes deficient in MKK4 showed impaired IL-2 production following activation of the T cell receptor, suggesting a key role of the MKK4/JNK pathway in inflammation. The mutation of the MKK4 gene in some carcinomas indicates that it may also have a role as a tumor suppressor. Control of the MKK4 activity and expression may provide novel approaches to cancer or anti-inflammatory therapy.

摘要

丝裂原活化蛋白激酶激酶4(MKK4)是丝裂原活化蛋白激酶激酶家族的成员之一,可响应细胞应激和促炎细胞因子,直接磷酸化并激活c-Jun氨基末端激酶(JNK)。JNK是丝裂原活化蛋白激酶家族的成员,也是应激激活蛋白激酶信号通路的关键组成部分。MKK4 mRNA在成年小鼠组织中广泛表达,但在骨骼肌和大脑中尤为丰富。缺乏MKK4基因的小鼠发生了异常的肝脏发育,并在胚胎第14天之前死亡。然而,已获得缺乏MKK4的细胞系,这些细胞系在响应某些(但不是全部)细胞应激时,JNK和AP-1依赖性转录活性的激活存在缺陷。此外,缺乏MKK4的T淋巴细胞在T细胞受体激活后,IL-2产生受损,这表明MKK4/JNK途径在炎症中起关键作用。某些癌症中MKK4基因的突变表明它可能也具有肿瘤抑制作用。对MKK4活性和表达的控制可能为癌症治疗或抗炎治疗提供新的方法。

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