Genetic Regulation of Cell Death: Insights from Autoinflammatory Diseases.

IF 26.9 1区 医学 Q1 IMMUNOLOGY
Hirotsugu Oda, Alessandro Annibaldi, Daniel L Kastner, Ivona Aksentijevich
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引用次数: 0

Abstract

Metazoans have evolved innate antimicrobial defenses that promote cellular survival and proliferation. Countering the inevitable molecular mechanisms by which microbes sabotage these pathways, multicellular organisms rely on an alternative, perhaps more ancient, strategy that is the immune equivalent of suicide bombing: Infection triggers cell death programs that summon localized or even systemic inflammation. The study of human genetics has now unveiled a level of complexity that refutes the naive view that cell death is merely a blunt instrument or an evolutionary afterthought. To the contrary, findings from patients with rare diseases teach us that cell death-induced inflammation is a sophisticated, tightly choreographed process. We herein review the emerging body of evidence describing a group of illnesses-inborn errors of cell death, which define many of the molecular building blocks and regulatory elements controlling cell death-induced inflammation in humans-and provide a possible road map to countering this process across the spectrum of rare and common illnesses.

细胞死亡的遗传调控:来自自身炎症性疾病的见解。
后生动物已经进化出先天的抗微生物防御,促进细胞存活和增殖。为了对抗微生物破坏这些途径的不可避免的分子机制,多细胞生物依靠另一种可能更古老的策略,这是一种相当于自杀式炸弹的免疫策略:感染触发细胞死亡程序,引发局部甚至全身炎症。人类遗传学的研究现在已经揭示了某种程度的复杂性,驳斥了细胞死亡只是一种钝器或进化后的想法的天真观点。相反,来自罕见疾病患者的发现告诉我们,细胞死亡引起的炎症是一个复杂的、紧密编排的过程。我们在此回顾了描述一组疾病的新证据——细胞死亡的先天性错误,它定义了许多分子构建块和控制人类细胞死亡诱导炎症的调节元件——并提供了一个可能的路线图,以应对罕见和常见疾病的这一过程。
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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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