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炎性小体在衰老过程中的潜在作用。

Potential Role of Inflammasomes in Aging.

作者信息

Lee Gilyoung, Lee Geun-Shik

机构信息

College of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon 24341, Republic of Korea.

出版信息

Int J Mol Sci. 2025 Jul 15;26(14):6768. doi: 10.3390/ijms26146768.

DOI:10.3390/ijms26146768
PMID:40725015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12296179/
Abstract

The aging process is associated with the emergence of low-grade, sterile inflammation, called inflammaging, which can accelerate aging-related diseases, such as neurodegenerative, cardiovascular, and musculoskeletal diseases. Recent studies have focused on the novel concept that inflammasomes represent a key innate immune pathway, mechanistically participating in aging-induced stress recognition. This review summarizes the advancements in inflammasome research related to aging. Particular attention is given to the close relationship between aging and inflammasomes and how these processes impact the health of the elderly. Inflammaging has various causes, such as metabolic disorders, changes in the gut microbiota, and immunosenescence. Hence, the connection between inflammasomes and these causes must be explored. This paper describes inflammasomes as a significant contributing factor among the mechanisms that make individuals susceptible to aging-related diseases and discusses the potential role of inflammasome regulation in effectively counteracting aging.

摘要

衰老过程与一种称为炎症衰老的低度无菌性炎症的出现有关,这种炎症会加速与衰老相关的疾病,如神经退行性疾病、心血管疾病和肌肉骨骼疾病。最近的研究集中在一个新的概念上,即炎性小体代表了一条关键的固有免疫途径,在机制上参与衰老诱导的应激识别。这篇综述总结了与衰老相关的炎性小体研究的进展。特别关注衰老与炎性小体之间的密切关系,以及这些过程如何影响老年人的健康。炎症衰老有多种原因,如代谢紊乱、肠道微生物群变化和免疫衰老。因此,必须探索炎性小体与这些原因之间的联系。本文将炎性小体描述为使个体易患与衰老相关疾病的机制中的一个重要促成因素,并讨论了炎性小体调节在有效对抗衰老方面的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f257/12296179/6e5f82813fc6/ijms-26-06768-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f257/12296179/6e5f82813fc6/ijms-26-06768-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f257/12296179/6e5f82813fc6/ijms-26-06768-g001.jpg

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本文引用的文献

1
The Role of Immunosenescence and Inflammaging in the Susceptibility of Older Adults to SARS-CoV-2 Infection.免疫衰老和炎症衰老在老年人对SARS-CoV-2感染易感性中的作用
Curr Pharm Biotechnol. 2025 Feb 13. doi: 10.2174/0113892010328697250210065420.
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Inflammaging and Brain Aging.炎症与大脑衰老。
Int J Mol Sci. 2024 Sep 30;25(19):10535. doi: 10.3390/ijms251910535.
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Characterization of age-associated inflammasome activation reveals tissue specific differences in transcriptional and post-translational inflammatory responses.
与年龄相关的炎性小体激活的特征揭示了转录和翻译后炎症反应中的组织特异性差异。
Immun Ageing. 2024 Sep 10;21(1):60. doi: 10.1186/s12979-024-00462-z.
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Participation of T cells in generating immune protection against cancers.T 细胞在产生针对癌症的免疫保护中的作用。
Pathol Res Pract. 2024 Oct;262:155534. doi: 10.1016/j.prp.2024.155534. Epub 2024 Aug 12.
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Anti-inflammatory effect of proanthocyanidins from blueberry through NF-κβ/NLRP3 signaling pathway and .蓝莓原花青素通过 NF-κβ/NLRP3 信号通路的抗炎作用及机制
Immunopharmacol Immunotoxicol. 2024 Aug;46(4):425-435. doi: 10.1080/08923973.2024.2358770. Epub 2024 May 30.
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NLRP3 inflammasome-mediated premature immunosenescence drives diabetic vascular aging dependent on the induction of perivascular adipose tissue dysfunction.NLRP3炎性小体介导的过早免疫衰老通过诱导血管周围脂肪组织功能障碍驱动糖尿病血管衰老。
Cardiovasc Res. 2025 Apr 15;121(1):77-96. doi: 10.1093/cvr/cvae079.
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Microglial ApoD-induced NLRC4 inflammasome activation promotes Alzheimer's disease progression.小胶质细胞载脂蛋白D诱导的NLRC4炎性小体激活促进阿尔茨海默病进展。
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Immun Ageing. 2024 Feb 5;21(1):14. doi: 10.1186/s12979-023-00395-z.
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Commun Biol. 2023 Dec 16;6(1):1274. doi: 10.1038/s42003-023-05684-3.
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