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靶向细胞坏死性凋亡:呼吸系统疾病治疗的新途径。

Targeting necroptosis: a promising avenue for respiratory disease treatment.

机构信息

School of Integrated Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan, 410208, People's Republic of China.

Hunan Provincial Key Laboratory of Vascular Biology and Translational Medicine, Changsha, Hunan, 410208, People's Republic of China.

出版信息

Cell Commun Signal. 2024 Aug 28;22(1):418. doi: 10.1186/s12964-024-01804-6.

DOI:10.1186/s12964-024-01804-6
PMID:39192326
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11350980/
Abstract

Respiratory diseases are a growing concern in public health because of their potential to endanger the global community. Cell death contributes critically to the pathophysiology of respiratory diseases. Recent evidence indicates that necroptosis, a unique form of programmed cell death (PCD), plays a vital role in the molecular mechanisms underlying respiratory diseases, distinguishing it from apoptosis and conventional necrosis. Necroptosis is a type of inflammatory cell death governed by receptor-interacting serine/threonine protein kinase 1 (RIPK1), RIPK3, and mixed-lineage kinase domain-like protein (MLKL), resulting in the release of intracellular contents and inflammatory factors capable of initiating an inflammatory response in adjacent tissues. These necroinflammatory conditions can result in significant organ dysfunction and long-lasting tissue damage within the lungs. Despite evidence linking necroptosis to various respiratory diseases, there are currently no specific alternative treatments that target this mechanism. This review provides a comprehensive overview of the most recent advancements in understanding the significance and mechanisms of necroptosis. Specifically, this review emphasizes the intricate association between necroptosis and respiratory diseases, highlighting the potential use of necroptosis as an innovative therapeutic approach for treating these conditions.

摘要

呼吸道疾病是公共卫生领域日益关注的问题,因为它们有可能危及全球社会。细胞死亡是呼吸道疾病病理生理学的关键因素。最近的证据表明,细胞程序性坏死(necroptosis),一种独特的细胞死亡形式(PCD),在呼吸道疾病的分子机制中起着至关重要的作用,使其有别于细胞凋亡和传统坏死。细胞程序性坏死由受体相互作用丝氨酸/苏氨酸蛋白激酶 1(RIPK1)、RIPK3 和混合谱系激酶结构域样蛋白(MLKL)调控,导致细胞内内容物和炎症因子的释放,从而引发相邻组织的炎症反应。这些坏死性炎症条件可导致肺部重要器官功能障碍和持久的组织损伤。尽管有证据表明细胞程序性坏死与各种呼吸道疾病有关,但目前尚无针对该机制的特定替代治疗方法。本综述全面概述了对细胞程序性坏死意义和机制的最新研究进展。具体而言,本综述强调了细胞程序性坏死与呼吸道疾病之间的复杂关联,突出了将细胞程序性坏死作为治疗这些疾病的创新治疗方法的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/46e5124263ab/12964_2024_1804_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/335aa12199b9/12964_2024_1804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/9a0eba219622/12964_2024_1804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/682a1bfa85e0/12964_2024_1804_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/afbd94fb1099/12964_2024_1804_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/46e5124263ab/12964_2024_1804_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/335aa12199b9/12964_2024_1804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/9a0eba219622/12964_2024_1804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/682a1bfa85e0/12964_2024_1804_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/afbd94fb1099/12964_2024_1804_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d216/11350980/46e5124263ab/12964_2024_1804_Fig5_HTML.jpg

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RIPK1 inhibitor ameliorates pulmonary injury by modulating the function of neutrophils and vascular endothelial cells.RIPK1抑制剂通过调节中性粒细胞和血管内皮细胞的功能来改善肺损伤。
Cell Death Discov. 2024 Mar 23;10(1):152. doi: 10.1038/s41420-024-01921-8.
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RIPK3 cleavage is dispensable for necroptosis inhibition but restricts NLRP3 inflammasome activation.
RIPK3 裂解对于抑制细胞坏死性凋亡是可有可无的,但限制了 NLRP3 炎性小体的激活。
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Immunogenic cell death in cancer: targeting necroptosis to induce antitumour immunity.肿瘤中的免疫原性细胞死亡:靶向坏死性凋亡诱导抗肿瘤免疫。
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