焦亡诱导与检测。

Q2 Immunology and Microbiology Current Protocols in Immunology Pub Date : 2018-08-01 Epub Date: 2018-07-20 DOI:10.1002/cpim.52
Andreas B den Hartigh, Susan L Fink
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引用次数: 11

摘要

焦亡是程序性促炎细胞死亡的一种形式,在宿主对感染的反应中起保护作用,但也可以促进致病性炎症。焦亡是由半胱氨酸蛋白酶caspase-1介导的。Caspase-1裂解gasdermin D,释放n端成孔结构域,该结构域插入质膜并驱动渗透裂解。Caspase-1还可以蛋白水解激活炎症细胞因子白介素1β (IL-1β)和IL-18。本单元描述了刺激热亡和评估随后质膜完整性损失的方法。我们还描述了一种定量释放IL-1β的ELISA。这些方法可以应用于许多不同类型的实验。©2018 by John Wiley & Sons, Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Pyroptosis Induction and Detection.

Pyroptosis is a form of programmed pro-inflammatory cell death that plays a protective role in the host response to infection, but can also promote pathogenic inflammation. Pyroptosis is mediated by the cysteine protease, caspase-1. Caspase-1 cleaves gasdermin D, releasing the N-terminal pore-forming domain, which inserts into the plasma membrane and drives osmotic lysis. Caspase-1 also proteolytically activates the inflammatory cytokines interleukin 1β (IL-1β) and IL-18. This unit describes methods for stimulating pyroptosis and assessing subsequent loss of plasma membrane integrity. We also describe an ELISA to quantify released IL-1β. These methods can be applied to many different types of experiments. © 2018 by John Wiley & Sons, Inc.

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Current Protocols in Immunology
Current Protocols in Immunology Immunology and Microbiology-Immunology
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