目标2
上睑下垂
先天免疫系统
吡喃结构域
炎症
半胱氨酸蛋白酶1
受体
免疫系统
促炎细胞因子
作者
Vincent Compan,Alberto Baroja-Mazo,Gloria Lopez-Castejon,Ana I. Gomez,Carlos Martinez,Diego Angosto,María T. Montero,Antonio S. Herranz,Eulalia Bazán,Diana Reimers,Victoriano Mulero,Pablo Pelegrín
出处
期刊:Immunity
[Elsevier]
日期:2012-09-21
卷期号:37 (3): 487-500
被引量:254
标识
DOI:10.1016/j.immuni.2012.06.013
摘要
Summary 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.
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