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JAK/STAT信号通路的负调控

Negative regulation of the JAK/STAT pathway.

作者信息

Starr R, Hilton D J

机构信息

Cooperative Research Centre for Cellular Growth Factors, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.

出版信息

Bioessays. 1999 Jan;21(1):47-52. doi: 10.1002/(SICI)1521-1878(199901)21:1<47::AID-BIES6>3.0.CO;2-N.

Abstract

Cytokines induce a variety of biological responses by binding to specific cell surface receptors and activating cytoplasmic signal transduction pathways, such as the JAK/STAT pathway. Although these responses are generally transient, few molecules have been characterised that switch the signal off. Several different steps of the signal transduction pathway appear to be targeted by negative regulators, including the receptor/ligand complex, JAK kinases, and STAT transcription factors. Negative regulation is achieved by dephosphorylation of signalling intermediates by protein tyrosine phosphatases such as SHP-1, and by proteolytic degradation. Recent studies have identified two new families of negative regulatory molecules, SOCS and PIAS, which function in novel ways to suppress signal transduction pathways. The duration and intensity of a cell's response to cytokine therefore appear to be determined by the net effect of several regulatory mechanisms.

摘要

细胞因子通过与特定的细胞表面受体结合并激活细胞质信号转导途径(如JAK/STAT途径)来诱导多种生物学反应。尽管这些反应通常是短暂的,但很少有分子被鉴定出能够关闭信号。信号转导途径的几个不同步骤似乎是负调控因子的作用靶点,包括受体/配体复合物、JAK激酶和STAT转录因子。负调控是通过蛋白酪氨酸磷酸酶(如SHP-1)对信号中间产物的去磷酸化作用以及蛋白水解降解来实现的。最近的研究已经鉴定出两个新的负调控分子家族,即SOCS和PIAS,它们以新的方式发挥作用来抑制信号转导途径。因此,细胞对细胞因子反应的持续时间和强度似乎是由几种调控机制的净效应决定的。

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