| Literature DB >> 29958799 |
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.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