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细胞死亡、炎症和疾病中的胱天蛋白酶。

Caspases in Cell Death, Inflammation, and Disease.

机构信息

Janssen Immunosciences, World Without Disease Accelerator, Pharmaceutical Companies of Johnson & Johnson, Beerse, 2340, Belgium.

Janssen Immunosciences, World Without Disease Accelerator, Pharmaceutical Companies of Johnson & Johnson, Beerse, 2340, Belgium; Department of Internal Medicine and Pediatrics, Ghent University, Ghent, 9000, Belgium.

出版信息

Immunity. 2019 Jun 18;50(6):1352-1364. doi: 10.1016/j.immuni.2019.05.020.

Abstract

Caspases are an evolutionary conserved family of cysteine proteases that are centrally involved in cell death and inflammation responses. A wealth of foundational insight into the molecular mechanisms that control caspase activation has emerged in recent years. Important advancements include the identification of additional inflammasome platforms and pathways that regulate activation of inflammatory caspases; the discovery of gasdermin D as the effector of pyroptosis and interleukin (IL)-1 and IL-18 secretion; and the existence of substantial crosstalk between inflammatory and apoptotic initiator caspases. A better understanding of the mechanisms regulating caspase activation has supported initial efforts to modulate dysfunctional cell death and inflammation pathways in a suite of communicable, inflammatory, malignant, metabolic, and neurodegenerative diseases. Here, we review current understanding of caspase biology with a prime focus on the inflammatory caspases and outline important topics for future experimentation.

摘要

Caspases 是一组进化上保守的半胱氨酸蛋白酶家族,它们在细胞死亡和炎症反应中起着核心作用。近年来,人们对控制半胱天冬酶激活的分子机制有了大量的基础性认识。重要的进展包括鉴定了额外的炎症小体平台和途径,这些平台和途径调节炎症半胱天冬酶的激活;发现了gasdermin D 作为细胞焦亡和白细胞介素 (IL)-1 和 IL-18 分泌的效应物;以及炎症和凋亡起始半胱天冬酶之间存在大量的串扰。对半胱天冬酶激活调节机制的更好理解,支持了最初在一系列传染性、炎症性、恶性、代谢性和神经退行性疾病中调节功能失调的细胞死亡和炎症途径的努力。在这里,我们综述了对半胱天冬酶生物学的现有理解,主要关注炎症半胱天冬酶,并概述了未来实验的重要课题。

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本文引用的文献

1
A20 prevents inflammasome-dependent arthritis by inhibiting macrophage necroptosis through its ZnF7 ubiquitin-binding domain.
Nat Cell Biol. 2019 Jun;21(6):731-742. doi: 10.1038/s41556-019-0324-3. Epub 2019 May 13.
2
Inflammasome Activation Triggers Blood Clotting and Host Death through Pyroptosis.
Immunity. 2019 Jun 18;50(6):1401-1411.e4. doi: 10.1016/j.immuni.2019.04.003. Epub 2019 May 7.
3
Caspase-1 initiates apoptosis in the absence of gasdermin D.
Nat Commun. 2019 May 7;10(1):2091. doi: 10.1038/s41467-019-09753-2.
4
cGAS in action: Expanding roles in immunity and inflammation.
Science. 2019 Mar 8;363(6431). doi: 10.1126/science.aat8657.
5
Macrophages, rather than DCs, are responsible for inflammasome activity in the GM-CSF BMDC model.
Nat Immunol. 2019 Apr;20(4):397-406. doi: 10.1038/s41590-019-0313-5. Epub 2019 Feb 11.
6
DPP8/DPP9 inhibition elicits canonical Nlrp1b inflammasome hallmarks in murine macrophages.
Life Sci Alliance. 2019 Feb 4;2(1). doi: 10.26508/lsa.201900313. Print 2019 Feb.
7
FAS and RAS related Apoptosis defects: From autoimmunity to leukemia.
Immunol Rev. 2019 Jan;287(1):50-61. doi: 10.1111/imr.12720.
10
Gasdermin D Promotes AIM2 Inflammasome Activation and Is Required for Host Protection against .
J Immunol. 2018 Dec 15;201(12):3662-3668. doi: 10.4049/jimmunol.1800788. Epub 2018 Nov 7.

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