神经侵袭性病毒感染过程中 RIP 激酶信号转导的结果

3区 医学 Q2 Medicine Current topics in microbiology and immunology Pub Date : 2023-01-01 DOI:10.1007/82_2020_204
Brian P Daniels, Andrew Oberst
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引用次数: 0

摘要

神经侵袭性病毒疾病对全球公共卫生造成了巨大且日益沉重的负担。尽管如此,人们对这些感染仍然知之甚少,而控制感染的保护性神经炎症反应和病理性神经炎症反应的分子机制也是一个需要深入研究的问题。最近的证据表明,坏死(一种程序性细胞死亡的免疫原性形式)可能是病毒性脑炎的发病机制之一。然而,协调坏死凋亡的受体相互作用蛋白(RIP)激酶 RIPK1 和 RIPK3 在中枢神经系统(CNS)中似乎也有意想不到的、不依赖于细胞死亡的功能,在神经侵入性感染期间促进有益的神经炎症。在此,我们回顾了这一领域新出现的证据,并进一步讨论了最近研究 RIPK 信号传导和坏死在中枢神经系统非感染性病理过程中的作用的工作,因为这些研究为 RIP 激酶发挥特殊神经免疫功能的潜力提供了重要的补充见解。
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Outcomes of RIP Kinase Signaling During Neuroinvasive Viral Infection.

Neuroinvasive viral diseases are a considerable and growing burden on global public health. Despite this, these infections remain poorly understood, and the molecular mechanisms that govern protective versus pathological neuroinflammatory responses to infection are a matter of intense investigation. Recent evidence suggests that necroptosis, an immunogenic form of programmed cell death, may contribute to the pathogenesis of viral encephalitis. However, the receptor-interacting protein (RIP) kinases that coordinate necroptosis, RIPK1 and RIPK3, also appear to have unexpected, cell death-independent functions in the central nervous system (CNS) that promote beneficial neuroinflammation during neuroinvasive infection. Here, we review the emerging evidence in this field, with additional discussion of recent work examining roles for RIPK signaling and necroptosis during noninfectious pathologies of the CNS, as these studies provide important additional insight into the potential for specialized neuroimmune functions for the RIP kinases.

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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: The review series Current Topics in Microbiology and Immunology provides a synthesis of the latest research findings in the areas of molecular immunology, bacteriology and virology. Each timely volume contains a wealth of information on the featured subject. This review series is designed to provide access to up-to-date, often previously unpublished information.
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