Department of Microbiology and Immunology, Stanford School of Medicine, Stanford University, 299 Campus Drive, Mail Code 5124, Stanford, CA 94305, United States.
Curr Opin Immunol. 2013 Feb;25(1):34-9. doi: 10.1016/j.coi.2012.11.009. Epub 2012 Dec 20.
Pattern recognition receptors recognize signals originating from pathogens and comprise a large part of the arsenal in innate immune responses. The NOD-like receptors (NLRs) are one particular class of these receptors that survey the cytoplasm for signs of pathogen invasion. Upon detection, they trigger the formation of a macromolecular complex called the inflammasome that is required for elimination of the pathogen, as well as amplifying a pro-inflammatory response. Although the core machinery has been defined, recent data emphasize the complexity of how NLR inflammasomes function. Here, we highlight new discoveries that reveal how precisely fine-tuned NLR inflammasome functions are, and how that may be modulated by antagonistic effects of concomitant inflammasome activation as well as novel regulatory factors.
模式识别受体识别源自病原体的信号,是先天免疫反应的重要组成部分。NOD 样受体(NLRs)是这些受体的一个特殊类别,它们在细胞质中检测病原体入侵的迹象。一旦检测到,它们就会触发一种叫做炎症小体的大分子复合物的形成,这种复合物对于消除病原体以及放大促炎反应是必需的。尽管核心机制已经确定,但最近的数据强调了 NLR 炎症小体如何发挥作用的复杂性。在这里,我们强调了新的发现,这些发现揭示了 NLR 炎症小体的功能是如何精确调整的,以及伴随的炎症小体激活以及新的调节因子如何通过拮抗作用来调节。