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全细胞程序性坏死:对缺血再灌注损伤机制的新见解。

PANoptosis: a new insight into the mechanism of ischaemia-reperfusion injury.

作者信息

Song Huapei, Liang Guangping, Wang Fengjun

机构信息

Institute of Burn Research, The First Affiliated Hospital of Army Medical University (The Third Military Medical University), State Key Laboratory of Trauma and Chemical Poisoning, Gaotanyan Street, Shapingba Disdrict, Chongqing 400038, China.

出版信息

Burns Trauma. 2025 Apr 10;13:tkaf026. doi: 10.1093/burnst/tkaf026. eCollection 2025.

DOI:10.1093/burnst/tkaf026
PMID:40625798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12230209/
Abstract

Programmed cell death, which occurs via modes such as apoptosis, necroptosis, and pyroptosis, is an important mechanism for host defence against pathogens and inflammation-mediated immune responses. Recently, interactions between various types of cell death have gradually been discovered. PANoptosis is a newly discovered mode of programmed cell death that involves apoptosis, necroptosis, and pyroptosis and is closely related to many diseases. Ischaemia-reperfusion injury (IRI) is common in patients with blood circulation disorders such as those related to burns, traumatic shock, surgery, organ transplantation, and thrombus. However, the literature on the role of PANoptosis in IRI is limited. Herein, we systematically described the emergence of PANoptosis as a cell death mode, clinical evidence of its occurrence, the molecular mechanisms of PANoptosis, and its role in IRI. This study is expected to provide novel approaches for the prevention and treatment of tissue and organ IRI after severe burns.

摘要

程序性细胞死亡通过凋亡、坏死性凋亡和焦亡等方式发生,是宿主抵御病原体和炎症介导的免疫反应的重要机制。最近,已逐渐发现各种类型细胞死亡之间的相互作用。PANoptosis是一种新发现的程序性细胞死亡模式,涉及凋亡、坏死性凋亡和焦亡,并且与许多疾病密切相关。缺血再灌注损伤(IRI)在患有血液循环障碍的患者中很常见,例如与烧伤、创伤性休克、手术、器官移植和血栓相关的患者。然而,关于PANoptosis在IRI中的作用的文献有限。在此,我们系统地描述了PANoptosis作为一种细胞死亡模式的出现、其发生的临床证据、PANoptosis的分子机制及其在IRI中的作用。本研究有望为严重烧伤后组织和器官IRI的防治提供新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2355/12230209/cfb2bc3af2dd/tkaf026f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2355/12230209/c0f6c72ceea4/tkaf026f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2355/12230209/cfb2bc3af2dd/tkaf026f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2355/12230209/c0f6c72ceea4/tkaf026f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2355/12230209/cfb2bc3af2dd/tkaf026f2.jpg

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本文引用的文献

1
Characterization of PANoptosis-related genes with immunoregulatory features in osteoarthritis.关节炎中具有免疫调节特征的 PANoptosis 相关基因的特征。
Int Immunopharmacol. 2024 Oct 25;140:112889. doi: 10.1016/j.intimp.2024.112889. Epub 2024 Aug 10.
2
The mechanosensitive Piezo1 channel exacerbates myocardial ischaemia/reperfusion injury by activating caspase-8-mediated PANoptosis.机械敏感性 Piezo1 通道通过激活 caspase-8 介导的 PANoptosis 加重心肌缺血/再灌注损伤。
Int Immunopharmacol. 2024 Sep 30;139:112664. doi: 10.1016/j.intimp.2024.112664. Epub 2024 Jul 14.
3
N6-methyladenosine demethylase ALKBH5 homologous protein protects against cerebral I/R injury though suppressing SNHG3-mediated neural PANoptosis: Involvement of m6A-related macromolecules in the diseases of nervous system.
N6-甲基腺苷去甲基酶 ALKBH5 同源蛋白通过抑制 SNHG3 介导的神经 PANoptosis 来保护大脑免受 I/R 损伤:神经系统疾病中 m6A 相关大分子的参与。
Int J Biol Macromol. 2024 Aug;274(Pt 2):133815. doi: 10.1016/j.ijbiomac.2024.133815. Epub 2024 Jul 10.
4
NLRC5 senses NAD depletion, forming a PANoptosome and driving PANoptosis and inflammation.NLRC5 感知 NAD 耗竭,形成 PANoptosome,并驱动 PANoptosis 和炎症反应。
Cell. 2024 Jul 25;187(15):4061-4077.e17. doi: 10.1016/j.cell.2024.05.034. Epub 2024 Jun 14.
5
ZBP1-mediated PANoptosis: A possible novel mechanism underlying the therapeutic effects of penehyclidine hydrochloride on myocardial ischemia-reperfusion injury.ZBP1 介导的 PANoptosis:盐酸戊乙奎醚治疗心肌缺血再灌注损伤的潜在新机制。
Int Immunopharmacol. 2024 Aug 20;137:112373. doi: 10.1016/j.intimp.2024.112373. Epub 2024 Jun 8.
6
Identification of PANoptosis-related subtypes, construction of a prognosis signature, and tumor microenvironment landscape of hepatocellular carcinoma using bioinformatic analysis and experimental verification.基于生物信息学分析和实验验证的肝细胞癌 PANoptosis 相关亚型鉴定、预后特征构建和肿瘤微环境分析。
Front Immunol. 2024 Apr 29;15:1323199. doi: 10.3389/fimmu.2024.1323199. eCollection 2024.
7
Ischemia-Reperfusion Injury in Kidney Transplantation: Mechanisms and Potential Therapeutic Targets.肾移植中的缺血再灌注损伤:机制与潜在治疗靶点
Int J Mol Sci. 2024 Apr 14;25(8):4332. doi: 10.3390/ijms25084332.
8
Identification and experimental validation of PYCARD as a crucial PANoptosis-related gene for immune response and inflammation in COPD.鉴定和实验验证 PYCARD 作为 COPD 免疫反应和炎症中关键的 PANoptosis 相关基因。
Apoptosis. 2024 Dec;29(11-12):2091-2107. doi: 10.1007/s10495-024-01961-6. Epub 2024 Apr 23.
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Propofol and salvianolic acid A synergistically attenuated cardiac ischemia-reperfusion injury in diabetic mice via modulating the CD36/AMPK pathway.丙泊酚和丹酚酸A通过调节CD36/AMPK途径协同减轻糖尿病小鼠的心脏缺血再灌注损伤。
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Brief Bioinform. 2024 Mar 27;25(3). doi: 10.1093/bib/bbae124.