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解析细胞死亡的复杂性:对意外性和程序性细胞死亡的见解

Navigating the complexities of cell death: Insights into accidental and programmed cell death.

作者信息

Lotfi Mohammad-Sadegh, Rassouli Fatemeh B

机构信息

Novel Diagnostics and Therapeutics Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran.

Novel Diagnostics and Therapeutics Research Group, Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran.

出版信息

Tissue Cell. 2024 Dec;91:102586. doi: 10.1016/j.tice.2024.102586. Epub 2024 Oct 16.

DOI:10.1016/j.tice.2024.102586
PMID:39426124
Abstract

Cell death is a critical biological phenomenon that can be categorized into accidental cell death (ACD) and programmed cell death (PCD), each exhibiting distinct signaling, mechanistic and morphological characteristics. This paper provides a comprehensive overview of seven types of ACD, including coagulative, liquefactive, caseous, fat, fibrinoid, gangrenous and secondary necrosis, discussing their pathological implications in conditions such as ischemia and inflammation. Additionally, we review eighteen forms of PCD, encompassing autophagy, apoptosis, necroptosis, pyroptosis, paraptosis, ferroptosis, anoikis, entosis, NETosis, eryptosis, parthanatos, mitoptosis, and newly recognized types such as methuosis, autosis, alkaliptosis, oxeiptosis, cuprotosis and erebosis. The implications of these cell death modalities for cellular processes, development, and disease-particularly in the context of neoplastic and neurodegenerative disorders-are also covered. Furthermore, we explore the crosstalk between various forms of PCD, emphasizing how apoptotic mechanisms can influence pathways like necroptosis and pyroptosis. Understanding this interplay is crucial for elucidating cellular responses to stress, as well as for its potential relevance in clinical applications and therapeutic strategies. Future research should focus on clarifying the molecular mechanisms that govern different forms of PCD and their interactions.

摘要

细胞死亡是一种关键的生物学现象,可分为意外性细胞死亡(ACD)和程序性细胞死亡(PCD),每种类型都具有独特的信号传导、机制和形态学特征。本文全面概述了七种类型的ACD,包括凝固性、液化性、干酪样、脂肪性、纤维素样、坏疽性和继发性坏死,并讨论了它们在缺血和炎症等情况下的病理意义。此外,我们回顾了十八种形式的PCD,包括自噬、凋亡、坏死性凋亡、焦亡、副凋亡、铁死亡、失巢凋亡、内吞凋亡、中性粒细胞胞外陷阱形成、红细胞凋亡、PARP-1依赖性坏死、线粒体凋亡,以及新发现的类型,如大自噬性细胞死亡、自噬性细胞死亡、碱中毒诱导的细胞死亡、氧化应激诱导的细胞死亡、铜死亡和衰老相关的细胞死亡。这些细胞死亡方式对细胞过程、发育和疾病的影响,特别是在肿瘤和神经退行性疾病背景下的影响,也在本文中进行了阐述。此外,我们探讨了各种形式的PCD之间的相互作用,强调凋亡机制如何影响坏死性凋亡和焦亡等途径。理解这种相互作用对于阐明细胞对压力的反应,以及其在临床应用和治疗策略中的潜在相关性至关重要。未来的研究应集中于阐明调控不同形式PCD及其相互作用的分子机制。

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