信号转导
细胞因子
炎症
肿瘤坏死因子α
细胞生物学
免疫学
生物
细胞因子信号抑制因子1
细胞因子信号抑制因子
促炎细胞因子
转录因子
白细胞介素
SOCS3
车站3
生物化学
抑制器
基因
作者
Toshitkatsu Hanada,Akihiko Yoshimura
标识
DOI:10.1016/s1359-6101(02)00026-6
摘要
Inflammation progresses by the action of pro-inflammatory cytokines, including interleukin-1 (IL-1), the tumor necrosis factor (TNF), gamma-interferon (IFNgamma), IL-12, IL-18, and the granulocyte-macrophage colony-stimulating factor, and is resolved by anti-inflammatory cytokines such as IL-4, IL-10, IL-13, IFNalpha, and the transforming growth factor (TGF)beta. The intracellular signal transduction pathways of these cytokines have been studied extensively, and these pathways ultimately activate transcription factors, such as NF-kappaB, Smad, and STATs. Recently, the negative-feedback regulation of these pathways has been identified. In this review, we provide examples of the relationship between cytokine signal transduction, negative-signal regulation, and inflammatory disease models. Furthermore, we illustrate several approaches for treating inflammatory diseases by modulating extracellular and intracellular signaling pathways.
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