Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK.
Immunity. 2012 Sep 21;37(3):487-500. doi: 10.1016/j.immuni.2012.06.013. Epub 2012 Sep 13.
Cell volume regulation is a primitive response to alterations in environmental osmolarity. The NLRP3 inflammasome is a multiprotein complex that senses pathogen- and danger-associated signals. Here, we report that, from fish to mammals, the basic mechanisms of cell swelling and regulatory volume decrease (RVD) are sensed via the NLRP3 inflammasome. We found that a decrease in extracellular osmolarity induced a K(+)-dependent conformational change of the preassembled NLRP3-inactive inflammasome during cell swelling, followed by activation of the NLRP3 inflammasome and caspase-1, which was controlled by transient receptor potential channels during RVD. Both mechanisms were necessary for interleukin-1β processing. Increased extracellular osmolarity prevented caspase-1 activation by different known NLRP3 activators. Collectively, our data identify cell volume regulation as a basic conserved homeostatic mechanism associated with the formation of the NLRP3 inflammasome and reveal a mechanism for NLRP3 inflammasome activation.
细胞体积调节是细胞对外界渗透压改变的原始反应。NLRP3 炎性小体是一种多蛋白复合物,可感知病原体和危险相关信号。在这里,我们报告称,从鱼类到哺乳动物,细胞肿胀和调节体积减少(RVD)的基本机制是通过 NLRP3 炎性小体感知的。我们发现,细胞肿胀期间细胞外渗透压降低诱导预组装的无活性 NLRP3 炎性小体发生依赖于 K(+)的构象变化,随后 NLRP3 炎性小体和半胱天冬酶-1 被激活,这在 RVD 期间受到瞬时受体电位通道的控制。这两种机制都是白细胞介素-1β加工所必需的。细胞外渗透压增加可防止不同已知的 NLRP3 激活剂激活半胱天冬酶-1。总之,我们的数据将细胞体积调节鉴定为与 NLRP3 炎性小体形成相关的基本保守稳态机制,并揭示了 NLRP3 炎性小体激活的一种机制。