Schroder Kate, Hertzog Paul J, Ravasi Timothy, Hume David A
Institute for Molecular Bioscience, University of Queensland, St. Lucia, Brisbane 4072, Australia.
J Leukoc Biol. 2004 Feb;75(2):163-89. doi: 10.1189/jlb.0603252. Epub 2003 Oct 2.
Interferon-gamma (IFN-gamma) coordinates a diverse array of cellular programs through transcriptional regulation of immunologically relevant genes. This article reviews the current understanding of IFN-gamma ligand, receptor, signal transduction, and cellular effects with a focus on macrophage responses and to a lesser extent, responses from other cell types that influence macrophage function during infection. The current model for IFN-gamma signal transduction is discussed, as well as signal regulation and factors conferring signal specificity. Cellular effects of IFN-gamma are described, including up-regulation of pathogen recognition, antigen processing and presentation, the antiviral state, inhibition of cellular proliferation and effects on apoptosis, activation of microbicidal effector functions, immunomodulation, and leukocyte trafficking. In addition, integration of signaling and response with other cytokines and pathogen-associated molecular patterns, such as tumor necrosis factor-alpha, interleukin-4, type I IFNs, and lipopolysaccharide are discussed.
γ干扰素(IFN-γ)通过对免疫相关基因的转录调控来协调一系列不同的细胞程序。本文综述了目前对IFN-γ配体、受体、信号转导和细胞效应的理解,重点是巨噬细胞反应,以及在感染过程中影响巨噬细胞功能的其他细胞类型的反应(程度相对较小)。讨论了当前的IFN-γ信号转导模型,以及信号调节和赋予信号特异性的因素。描述了IFN-γ的细胞效应,包括病原体识别、抗原加工和呈递的上调、抗病毒状态、细胞增殖的抑制和对细胞凋亡的影响、杀菌效应功能的激活、免疫调节和白细胞运输。此外,还讨论了信号转导和反应与其他细胞因子和病原体相关分子模式(如肿瘤坏死因子-α、白细胞介素-4、I型IFN和脂多糖)的整合。