Symons Antony, Beinke Soren, Ley Steven C
Division of Immune Cell Biology, National Institute for Medical Research, Mill Hill, London NW7 1AA, UK.
Trends Immunol. 2006 Jan;27(1):40-8. doi: 10.1016/j.it.2005.11.007. Epub 2005 Dec 13.
Toll-like receptors, which respond to invariant microbial molecules, and receptors for the proinflammatory cytokines tumour necrosis factor and interleukin-1 are crucial for initiation and regulation of innate immune responses. These receptors activate each of the major mitogen-activated protein (MAP) kinase subtypes, extracellular signal-regulated protein kinases, c-Jun amino-terminal kinases and p38 MAP kinases, which are crucial for cell survival and controlling the expression of immune mediators. Here we discuss recent studies characterizing the specific MAP kinase kinase kinases (MAP 3-kinases) that link MAP kinases to receptors involved in innate immunity and the mechanisms by which the activity of MAP 3-kinases is regulated by such receptors.
Toll样受体可对恒定的微生物分子作出反应,而促炎细胞因子肿瘤坏死因子和白细胞介素-1的受体对于先天免疫反应的启动和调节至关重要。这些受体激活每种主要的丝裂原活化蛋白(MAP)激酶亚型、细胞外信号调节蛋白激酶、c-Jun氨基末端激酶和p38 MAP激酶,它们对于细胞存活和控制免疫介质的表达至关重要。在此,我们讨论了最近的研究,这些研究描述了将MAP激酶与先天免疫相关受体联系起来的特定MAP激酶激酶激酶(MAP 3激酶),以及此类受体调节MAP 3激酶活性的机制。