干扰素的诱导和作用机制。

J Content
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引用次数: 0

摘要

由于发现干扰素应答构成了对感染性微生物的先天免疫和适应性免疫之间的有效过渡,这些细胞因子的功能和作用得到了更好的理解。干扰素作用于特定的细胞受体,激活明确的转导途径,增强数百种不同的干扰素刺激基因(ISGs)的表达,从而导致所谓的抗病毒状态。其中一些基因,包括那些编码蛋白质的基因(如PKR、OAS和ADAR1),依赖于细胞内双链RNA的存在来激活它们的酶功能,这些基因被更详细地研究了。近年来,在了解I型干扰素表达是如何被诱导以应对病毒感染方面取得了相当大的进展。这意味着几种toll样受体(TLRs)和几种新描述的细胞质蛋白传感器(RIG-I, MDA5, DAI)检测病毒核酸的存在并转导细胞内信号,导致干扰素调节因子(IRFs)家族的几个成员的激活,这些成员是I型干扰素表达所必需的,或者直接激活一些ISGs本身。这些转导途径的发现主要来源于对基因缺陷细胞和动物的研究。这些蛋白的重要性通过发现几种病毒编码拮抗剂得到进一步证实,这些拮抗剂可以特异性地中断I型干扰素诱导或作用的各个步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of induction and action of interferons.

Since the discovery that interferons responses constitute an efficient transition between innate and adaptive immunity to infectious microorganisms, the function and role of these cytokines are better understood. Interferons act on specific cell receptors, which activate well-defined transduction pathways to enhance the expression of hundreds of different Interferon-Stimulated Genes (ISGs) leading to the so-called antiviral state. Several of these genes including those encoding proteins (such as PKR, OAS, and ADAR1) depending on the presence of intracellular double stranded RNA for the activation of their enzymatic function, were studied in more detail. Considerable progress has been made recently in understanding how type I interferons expression is induced in response to virus infection. These imply several Toll-like Receptors (TLRs) and several newly described cytoplasmic protein sensors (RIG-I, MDA5, DAI) that detect the presence of viral nucleic acids and transduce intracellular signals leading to the activation of several members of the family of interferon regulatory factors (IRFs) required for the expression of type I interferons or directly some of the ISGs themselves. The discovery of these transduction pathways derives largely from the study of gene deficient cells and animals. The importance of these proteins is further attested by the discovery of several virally encoded antagonists that can interrupt specifically various steps of either the induction or the action of type I interferons.

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