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NLRP7 包含的炎性体介导体人巨噬细胞中微生物脂肽的识别。

An NLRP7-containing inflammasome mediates recognition of microbial lipopeptides in human macrophages.

机构信息

Division of Rheumatology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

出版信息

Immunity. 2012 Mar 23;36(3):464-76. doi: 10.1016/j.immuni.2012.02.001. Epub 2012 Feb 21.

Abstract

Cytosolic pathogen- and damage-associated molecular patterns are sensed by pattern recognition receptors, including members of the nucleotide-binding domain and leucine-rich repeat-containing gene family (NLR), which cause inflammasome assembly and caspase-1 activation to promote maturation and release of the inflammatory cytokines interleukin-1β (IL-1β) and IL-18 and induction of pyroptosis. However, the contribution of most of the NLRs to innate immunity, host defense, and inflammasome activation and their specific agonists are still unknown. Here we describe identification and characterization of an NLRP7 inflammasome in human macrophages, which is induced in response to microbial acylated lipopeptides. Activation of NLRP7 promoted ASC-dependent caspase-1 activation, IL-1β and IL-18 maturation, and restriction of intracellular bacterial replication, but not caspase-1-independent secretion of the proinflammatory cytokines IL-6 and tumor necrosis factor-α. Our study therefore increases our currently limited understanding of NLR activation, inflammasome assembly, and maturation of IL-1β and IL-18 in human macrophages.

摘要

细胞质病原体和损伤相关分子模式被模式识别受体识别,包括核苷酸结合域和富含亮氨酸重复序列基因家族(NLR)的成员,这些受体导致炎症小体组装和半胱天冬酶-1 的激活,以促进炎性细胞因子白细胞介素-1β(IL-1β)和 IL-18 的成熟和释放,并诱导细胞焦亡。然而,大多数 NLR 对先天免疫、宿主防御以及炎症小体激活及其特定激动剂的贡献仍然未知。在这里,我们描述了人巨噬细胞中 NLRP7 炎症小体的鉴定和特征,该炎症小体响应微生物酰化脂肽而被诱导。NLRP7 的激活促进 ASC 依赖性半胱天冬酶-1 的激活、IL-1β 和 IL-18 的成熟以及细胞内细菌复制的限制,但不促进促炎细胞因子 IL-6 和肿瘤坏死因子-α的非半胱天冬酶-1 依赖性分泌。因此,我们的研究增加了我们目前对人类巨噬细胞中 NLR 激活、炎症小体组装和 IL-1β 和 IL-18 成熟的有限理解。

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