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Janus 激酶的分子结构与功能:对抑制剂开发的影响。

Molecular Structure and Function of Janus Kinases: Implications for the Development of Inhibitors.

机构信息

Department of Gastroenterology, Institut d'Investigacions Biomèdiques August Pi i Sunyer [IDIBAPS] - CIBEREHD, Barcelona, Spain.

出版信息

J Crohns Colitis. 2020 Aug 1;14(Supplement_2):S713-S724. doi: 10.1093/ecco-jcc/jjz206.

Abstract

Cytokines can trigger multiple signalling pathways, including Janus tyrosine kinases [JAK] and signal transducers and activators of transcription [STATS] pathways. JAKs are cytoplasmic proteins that, following the binding of cytokines to their receptors, transduce the signal by phosphorylating STAT proteins which enter the nuclei and rapidly target gene promoters to regulate gene transcription. Due to the critical involvement of JAK proteins in mediating innate and adaptive immune responses, these family of kinases have become desirable pharmacological targets in inflammatory diseases, including ulcerative colitis and Crohn's disease. In this review we provide an overview of the main cytokines that signal through the JAK/STAT pathway and the available in vivo evidence on mutant or deleted JAK proteins, and discuss the implications of pharmacologically targeting this kinase family in the context of inflammatory diseases.

摘要

细胞因子可以触发多种信号通路,包括 Janus 酪氨酸激酶 [JAK] 和信号转导子和转录激活子 [STAT] 通路。JAK 是细胞质蛋白,在细胞因子与其受体结合后,通过磷酸化 STAT 蛋白转导信号,STAT 蛋白进入细胞核并迅速靶向基因启动子以调节基因转录。由于 JAK 蛋白在介导先天和适应性免疫反应中的关键作用,这些激酶家族已成为炎症性疾病(包括溃疡性结肠炎和克罗恩病)中理想的药物靶点。在这篇综述中,我们概述了通过 JAK/STAT 通路信号传递的主要细胞因子以及关于突变或缺失 JAK 蛋白的体内现有证据,并讨论了在炎症性疾病背景下靶向该激酶家族的药理学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a843/7395311/60477a4e08c2/jjz206f0001.jpg

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