Rudolf-Buchheim-Institute of Pharmacology, Justus-Liebig-University Giessen, 35392 Giessen, Germany.
Sci Signal. 2010 Jan 19;3(105):cm2. doi: 10.1126/scisignal.3105cm2.
The innate immune system senses molecular patterns from invading microorganisms. Once activated, it orchestrates the inflammatory response by secreting proinflammatory cytokines, such as interleukin-1 (IL-1)-type cytokines, in particular IL-1beta. IL-1 mediates the expression of a vast array of genes involved in secondary inflammation. IL-1-responsive genes coordinate all aspects of local inflammation and also attract and activate cells of the adaptive immune system at sites of infection. Moreover, the innate immune system can also sense a wide range of nonmicrobial molecular patterns that represent danger or damage signals. These signals activate the NALP3-inflammasome pathway, which plays a central role in acute and chronic sterile inflammation. Here, we describe the essential components of the NALP3-inflammasome that control processing and release of IL-1beta.
天然免疫系统可识别来自入侵微生物的分子模式。一旦被激活,它就会通过分泌促炎细胞因子(如白细胞介素-1(IL-1)-样细胞因子,特别是 IL-1β)来协调炎症反应。IL-1 介导与二次炎症相关的大量基因的表达。IL-1 响应基因协调局部炎症的各个方面,并在感染部位吸引和激活适应性免疫系统的细胞。此外,天然免疫系统还可以感知广泛的非微生物分子模式,这些模式代表危险或损伤信号。这些信号激活 NALP3-炎症小体途径,该途径在急性和慢性无菌性炎症中起核心作用。在这里,我们描述了控制 IL-1β加工和释放的 NALP3-炎症小体的基本组成部分。