Literature DB >> 29958799

The TWIK2 Potassium Efflux Channel in Macrophages Mediates NLRP3 Inflammasome-Induced Inflammation.

Anke Di1, Shiqin Xiong1, Zhiming Ye1, R K Subbarao Malireddi2, Satoshi Kometani1, Ming Zhong1, Manish Mittal1, Zhigang Hong1, Thirumala-Devi Kanneganti2, Jalees Rehman1, Asrar B Malik3.   

Abstract

Potassium (K+) efflux across the plasma membrane is thought to be an essential mechanism for ATP-induced NLRP3 inflammasome activation, yet the identity of the efflux channel has remained elusive. Here we identified the two-pore domain K+ channel (K2P) TWIK2 as the K+ efflux channel triggering NLRP3 inflammasome activation. Deletion of Kcnk6 (encoding TWIK2) prevented NLRP3 activation in macrophages and suppressed sepsis-induced lung inflammation. Adoptive transfer of Kcnk6-/- macrophages into mouse airways after macrophage depletion also prevented inflammatory lung injury. The K+ efflux channel TWIK2 in macrophages has a fundamental role in activating the NLRP3 inflammasome and consequently mediates inflammation, pointing to TWIK2 as a potential target for anti-inflammatory therapies.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  KCNK6; NLRP3 inflammasome; P2X7 receptor; TWIK2; inflammation; potassium channel

Mesh:

Substances:

Year:  2018        PMID: 29958799      PMCID: PMC6051907          DOI: 10.1016/j.immuni.2018.04.032

Source DB:  PubMed          Journal:  Immunity        ISSN: 1074-7613            Impact factor:   31.745


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