Department of Laboratory Medicine, University of California, San Francisco, 94143, USA.
Cold Spring Harb Perspect Biol. 2011 Mar 1;3(3):a002352. doi: 10.1101/cshperspect.a002352.
The response of innate immune cells to growth factors, immune complexes, extracellular matrix proteins, cytokines, pathogens, cellular damage, and many other stimuli is regulated by a complex net of intracellular signal transduction pathways. The majority of these pathways are either initiated or modulated by Src-family or Syk tyrosine kinases present in innate cells. The Src-family kinases modulate the broadest range of signaling responses, including regulating immunoreceptors, C-type lectins, integrins, G-protein-coupled receptors, and many others. Src-family kinases also modulate the activity of other kinases, including the Tec-family members as well as FAK and Pyk2. Syk kinase is required for initiation of signaling involving receptors that utilize immunoreceptor tyrosine activation (ITAM) domains. This article reviews the major activating and inhibitory signaling pathways regulated by these cytoplasmic tyrosine kinases, illuminating the many examples of signaling cross talk between pathways.
先天免疫细胞对生长因子、免疫复合物、细胞外基质蛋白、细胞因子、病原体、细胞损伤和许多其他刺激的反应是由细胞内信号转导途径的复杂网络调节的。这些途径中的大多数是由先天细胞中存在的Src 家族或 Syk 酪氨酸激酶启动或调节的。Src 家族激酶调节最广泛的信号反应,包括调节免疫受体、C 型凝集素、整合素、G 蛋白偶联受体等。Src 家族激酶还调节其他激酶的活性,包括 Tec 家族成员以及 FAK 和 Pyk2。Syk 激酶是涉及利用免疫受体酪氨酸激活 (ITAM) 结构域的受体的信号转导起始所必需的。本文综述了这些细胞质酪氨酸激酶调节的主要激活和抑制信号通路,阐明了通路之间信号交叉对话的许多实例。