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引用次数: 18
摘要
TNF是一种有效的细胞因子,在调节多种细胞反应和协调免疫和炎症反应中发挥重要作用。TNF通过结合TNFR1-和tnfr2特异性细胞表面受体发挥其作用,这些受体激活了许多细胞内信号级联反应,包括核因子κ b (nf - κ b)和丝裂原激活的蛋白激酶途径。NF-kappaB的激活通过将信息从细胞表面TNF受体传递到细胞核来介导TNF的许多功能,在细胞核中它协调一个基因表达程序,使细胞存活并引发其反应。TNF与NF-kappaB信号通路的密切相互作用通过在NF-kappaB信号成分缺陷的转基因和敲除小鼠中获得的结果得到强调,TNF已被证明有助于在这些小鼠中观察到的不同病理。本章重点讨论TNF在NF-kappaB缺乏引起的病理中的功能,并讨论这些发现对我们理解炎症性疾病的意义。
Role of TNF in pathologies induced by nuclear factor kappaB deficiency.
TNF is a potent cytokine with an important role in the regulation of a multitude of cellular responses and in coordinating immune and inflammatory reactions. TNF exerts its effects by binding to the TNFR1- and TNFR2-specific cell surface receptors, which activate a number of intracellular signaling cascades including the nuclear factor kappaB (NF-kappaB) and mitogen-activated protein kinase pathways. Activation of NF-kappaB mediates many of the functions of TNF by transmitting information from the cell surface TNF receptors to the nucleus, where it coordinates a gene expression program that allows the cell to survive and elicit its responses. The intimate interplay of TNF with the NF-kappaB signaling pathway is highlighted by results obtained in transgenic and knockout mice with defects in NF-kappaB signaling components, where TNF has been shown to contribute to different pathologies observed in these mice. This chapter focuses on the function of TNF in pathologies induced by NF-kappaB deficiency and discusses the implications of these findings for our understanding of inflammatory diseases.