| Literature DB >> 22981536 |
Vincent Compan1, Alberto Baroja-Mazo, Gloria López-Castejón, Ana I Gomez, Carlos M Martínez, Diego Angosto, María T Montero, Antonio S Herranz, Eulalia Bazán, Diana Reimers, Victoriano Mulero, Pablo Pelegrín.
Abstract
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.Mesh:
Substances:
Year: 2012 PMID: 22981536 DOI: 10.1016/j.immuni.2012.06.013
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745