IFN-γ signaling-Does it mean JAK-STAT?

被引：245

作者：

Gough, Daniel J. ^{[2
]}

Levy, David E. ^{[2
]}

Johnstone, Ricky W. ^{[1
]}

Clarke, Christopher J. ^{[1
]}

机构：

[1] Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic, Australia

[2] NYU, Langone Sch Med, Dept Pathol, NYU Canc Inst, New York, NY 10016 USA

来源：

CYTOKINE & GROWTH FACTOR REVIEWS | 2008年 / 19卷 / 5-6期

关键词：

Interferon gamma; STAT1; independent;

D O I：

10.1016/j.cytogfr.2008.08.004

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The molecular pathways involved in the cellular response to interferon (IFN)gamma have been the focus of much research effort due to their importance in host defense against infection and disease, as well as its potential as a therapeutic agent. The discovery of the JAK-STAT signaling pathway greatly enhanced our understanding of the mechanism of IFN gamma-mediated gene transcription. However, in recent years it has become apparent that other pathways, including MAP kinase, PI3-K, CaMKII and NF-kappa B, either co-operate with or act in parallel to JAK-STAT signaling to regulate the many facets of IFN gamma biology in a gene- and cell type-specific manner. The complex interactions between JAK/STAT and alternate pathways and the impact of these signaling networks on the biological responses to IFN gamma are beginning to be understood. This review summarizes and appraises current advances in our understanding of these complex interactions, their specificity and proposed biological outcomes. (c) 2008 Elsevier Ltd. All rights reserved.

引用

页码：383 / 394

页数：12

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