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激活 NLRP3 炎性小体的方法。

Methods to Activate the NLRP3 Inflammasome.

机构信息

Faculty of Medicine, Institute of Neuropathology, Medical Center - University of Freiburg, Freiburg, Germany.

Faculty of Biology, University of Freiburg, Freiburg, Germany.

出版信息

Methods Mol Biol. 2023;2696:169-197. doi: 10.1007/978-1-0716-3350-2_12.

DOI:10.1007/978-1-0716-3350-2_12
PMID:37578723
Abstract

The inflammasome-nucleating cytoplasmic sensor protein NLRP3 (NACHT-, LRR, and PYD domains-containing protein 3, also known as NOD-like receptor pyrin domain-containing 3, NALP3, or cryopyrin) is triggered by a broad spectrum of sterile endogenous danger signals and environmental irritants. Upon activation, NLRP3 engages the adapter protein ASC that in turn recruits the third inflammasome component, the protease caspase-1. Subsequent caspase-1 activation leads to its auto-processing and maturation of the leaderless IL-1 family cytokines IL-1β and IL-18 as well as cleavage of the pore-forming protein Gasdermin D (GSDMD). GSDMD plasma membrane pores, formed by its N-terminus, facilitate IL-1 release and, typically, subsequent cell lysis (pyroptosis). This protocol explains standard methods, which are routinely used in our laboratory to study NLRP3 inflammasome biology in vitro. It includes experimental approaches using primary murine bone marrow-derived macrophages (BMDMs) and bone marrow-derived dendritic cells (BMDCs), human peripheral blood mononuclear cells (PBMCs), as well as inflammasome-competent cell lines (HoxB8 and THP-1 cells). The protocol covers the use of a broad spectrum of established NLRP3 activators and outlines the use of common inhibitors blocking NLRP3 itself or its upstream triggering events. We also provide guidelines for experimental set-up and crucial experimental controls to investigate NLRP3 inflammasome signaling or study new activators and inhibitors.

摘要

胞质模式识别受体 NLRP3(NACHT、LRR 和 PYD 结构域包含蛋白 3,也称为 NOD 样受体吡咯结构域包含蛋白 3、NALP3 或冷诱导 RNA 结合蛋白 3)被广泛的内源性无菌危险信号和环境刺激物激活。NLRP3 激活后,与衔接蛋白 ASC 结合,后者招募第三个炎症小体成分半胱氨酸蛋白酶-1(caspase-1)。随后 caspase-1 的激活导致其自身加工和无领导的白细胞介素(IL)家族细胞因子 IL-1β 和 IL-18 的成熟,以及孔形成蛋白 Gasdermin D(GSDMD)的切割。GSDMD 细胞膜孔由其 N 端形成,促进 IL-1 的释放,通常随后导致细胞裂解(细胞焦亡)。本方案介绍了我们实验室常规用于体外研究 NLRP3 炎症小体生物学的标准方法。它包括使用原代小鼠骨髓来源的巨噬细胞(BMDMs)和骨髓来源的树突状细胞(BMDCs)、人外周血单核细胞(PBMCs)以及炎症小体活性细胞系(HoxB8 和 THP-1 细胞)的实验方法。该方案涵盖了广泛使用的已建立的 NLRP3 激活剂,并概述了使用常见抑制剂阻断 NLRP3 本身或其上游触发事件的方法。我们还提供了实验设置和关键实验对照的指南,以研究 NLRP3 炎症小体信号或研究新的激活剂和抑制剂。

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Methods to Activate the NLRP3 Inflammasome.激活 NLRP3 炎性小体的方法。
Methods Mol Biol. 2023;2696:169-197. doi: 10.1007/978-1-0716-3350-2_12.
2
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NLRP3 inflammasome activation triggers gasdermin D-independent inflammation.NLRP3 炎性小体激活触发 Gasdermin D 非依赖性炎症。
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The zebrafish NLRP3 inflammasome has functional roles in ASC-dependent interleukin-1β maturation and gasdermin E-mediated pyroptosis.斑马鱼 NLRP3 炎性小体在 ASC 依赖性白细胞介素-1β成熟和 GSDME 介导的细胞焦亡中发挥功能作用。
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IAPP/amylin deposition, which is correlated with expressions of ASC and IL-1β in β-cells of Langerhans' islets, directly initiates NLRP3 inflammasome activation.IAPP/胰岛淀粉样多肽沉积与胰岛β细胞中 ASC 和 IL-1β 的表达相关,直接引发 NLRP3 炎症小体激活。
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本文引用的文献

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NLRP3 cages revealed by full-length mouse NLRP3 structure control pathway activation.全长小鼠 NLRP3 结构揭示 NLRP3 小体控制通路激活。
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Caspase-8-dependent gasdermin D cleavage promotes antimicrobial defense but confers susceptibility to TNF-induced lethality.半胱天冬酶-8 依赖性的 GSDMD 切割促进抗菌防御,但易感染 TNF 诱导的致死性。
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The N-end rule ubiquitin ligase UBR2 mediates NLRP1B inflammasome activation by anthrax lethal toxin.N-端规则泛素连接酶 UBR2 通过炭疽致死毒素介导 NLRP1B 炎性体激活。
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Structural mechanism for NEK7-licensed activation of NLRP3 inflammasome.NEK7 许可激活 NLRP3 炎症小体的结构机制。
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