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炎症小体多样性:探索先天免疫反应的新前沿。

Inflammasome diversity: exploring novel frontiers in the innate immune response.

机构信息

Department of Biological Science, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.

Center for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon, Republic of Korea.

出版信息

Trends Immunol. 2024 Apr;45(4):248-258. doi: 10.1016/j.it.2024.02.004. Epub 2024 Mar 21.

Abstract

Pathogens elicit complex mammalian immune responses by activating multiple sensors within inflammasomes, which recognize diverse pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs). This simultaneous activation induces the formation of protein complexes referred to as multiple inflammasomes, that orchestrate a spectrum of programmed cell death pathways, including pyroptosis, apoptosis, and necroptosis. This concept is crucial for comprehending the complexity of the innate immune system's response to diverse pathogens and its implications for various diseases. Novel contributions here include emphasizing simultaneous sensor activation by pathogens, proposing the existence of multiple inflammasome complexes, and advocating for further exploration of their structural basis. Understanding these mechanisms may offer insights into disease pathogenesis, paving the way for potential therapeutic interventions targeting inflammasome-mediated immune responses.

摘要

病原体通过激活炎症小体中的多种传感器来引发复杂的哺乳动物免疫反应,这些传感器可以识别多种病原体相关分子模式 (PAMPs) 和损伤相关分子模式 (DAMPs)。这种同时激活诱导了被称为多炎症小体的蛋白质复合物的形成,这些复合物协调了一系列程序性细胞死亡途径,包括细胞焦亡、细胞凋亡和细胞坏死。这一概念对于理解先天免疫系统对多种病原体的反应的复杂性及其对各种疾病的影响至关重要。这里的新贡献包括强调病原体的同时传感器激活,提出多炎症小体复合物的存在,并主张进一步探索其结构基础。理解这些机制可能为疾病发病机制提供新的见解,并为针对炎症小体介导的免疫反应的潜在治疗干预铺平道路。

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