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细胞程序性死亡方式:细胞坏死、细胞焦亡与细胞凋亡。

Necroptosis, pyroptosis and apoptosis: an intricate game of cell death.

机构信息

Institute of Innate Immunity, University Hospitals Bonn, University of Bonn, Bonn, NRW, Germany.

Department of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

Cell Mol Immunol. 2021 May;18(5):1106-1121. doi: 10.1038/s41423-020-00630-3. Epub 2021 Mar 30.


DOI:10.1038/s41423-020-00630-3
PMID:33785842
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8008022/
Abstract

Cell death is a fundamental physiological process in all living organisms. Its roles extend from embryonic development, organ maintenance, and aging to the coordination of immune responses and autoimmunity. In recent years, our understanding of the mechanisms orchestrating cellular death and its consequences on immunity and homeostasis has increased substantially. Different modalities of what has become known as 'programmed cell death' have been described, and some key players in these processes have been identified. We have learned more about the intricacies that fine tune the activity of common players and ultimately shape the different types of cell death. These studies have highlighted the complex mechanisms tipping the balance between different cell fates. Here, we summarize the latest discoveries in the three most well understood modalities of cell death, namely, apoptosis, necroptosis, and pyroptosis, highlighting common and unique pathways and their effect on the surrounding cells and the organism as a whole.

摘要

细胞死亡是所有生物体的基本生理过程。它的作用范围从胚胎发育、器官维持和衰老,到免疫反应和自身免疫的协调。近年来,我们对调节细胞死亡的机制及其对免疫和内稳态的影响有了更深入的了解。已经描述了不同形式的所谓“程序性细胞死亡”,并且已经确定了这些过程中的一些关键参与者。我们对微调常见参与者活性并最终塑造不同类型细胞死亡的复杂性有了更多的了解。这些研究强调了在不同细胞命运之间取得平衡的复杂机制。在这里,我们总结了三种最被理解的细胞死亡方式(即细胞凋亡、细胞坏死和细胞焦亡)的最新发现,强调了它们的共同和独特途径及其对周围细胞和整个生物体的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/75ad829a4feb/41423_2020_630_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/6a24d22e26a2/41423_2020_630_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/5a397d32c0b8/41423_2020_630_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/12288374e40b/41423_2020_630_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/75ad829a4feb/41423_2020_630_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/6a24d22e26a2/41423_2020_630_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/5a397d32c0b8/41423_2020_630_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/12288374e40b/41423_2020_630_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1132/8093267/75ad829a4feb/41423_2020_630_Fig4_HTML.jpg

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引用本文的文献

[1]
The molecular mechanisms and therapeutic implications of PANoptosis in ischemic diseases.

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[2]
NLRP3 Inflammasome Activation Restricts Viral Replication by Inducing Pyroptosis in Chicken HD11 Cells During Infectious Bronchitis Virus Infection.

Biology (Basel). 2025-8-14

[3]
Regulated cell death in fungi from a comparative immunology perspective.

Cell Death Differ. 2025-9-3

[4]
FGFC1 overcomes Ara-C resistance in acute myeloid leukemia by inducing apoptosis and pyroptosis.

Front Pharmacol. 2025-8-14

[5]
Construction and immunohistochemical validation of a necroptosis-related prognostic signature in bladder cancer and its association with tumor immune infiltration.

Front Genet. 2025-8-14

[6]
Recent advances in copper sulfide nanoparticles for cancer diagnosis and therapy.

Mater Today Bio. 2025-8-13

[7]
MAP3K13-232aa encoded by circMAP3K13 enhances cisplatin-induced pyroptosis by directly binding to IKKα in gastric adenocarcinoma.

Cell Death Dis. 2025-9-1

[8]
From gum inflammation to oral cancers: pyroptosis as the molecular torchbearer in periodontitis-driven carcinogenesis.

Discov Oncol. 2025-9-1

[9]
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[10]
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本文引用的文献

[1]
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[2]
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Cell Death Dis. 2020-8-14

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