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The NLRP3 Inflammasome Renders Cell Death Pro-inflammatory

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 430, Issue 2, Pages 133-141

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2017.11.013

Keywords

NLRP3; Inflammasome; IL-1 beta; Potassium efflux; Inflammation; programmed cell death

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NLRP3 is the most studied inflammasome sensor due to its crucial involvement in sterile and infection-triggered inflammation. Although its molecular mode of activation remains to be defined, it is well established that low intracellular potassium concentrations result in its activation. This functionality allows the classical NLRP3 pathway to serve as a highly sensitive, but non-specific surveillance mechanism responding to any type of perturbation that breaches plasma membrane integrity and the associated potassium gradient across the membrane. Here, we review our current knowledge on potassium efflux-dependent NLRP3 activation, with a special focus on how major cell death programs are rendered pro-inflammatory by secondary NLRP3 activation. Apart from the alternative inflammasome as the major exception to the rule, this connection explains the fundamental importance of NLRP3 in cell death-associated inflammation and firmly establishes NLRP3 as a principal surveillance mechanism of cellular integrity. (C) 2017 Published by Elsevier Ltd.

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