炎症体
流出
炎症
钾通道
细胞生物学
生物
巨噬细胞
免疫学
化学
生物物理学
生物化学
体外
作者
Anke Di,Shan Xiong,Zhiming Ye,R. K. Subbarao Malireddi,Satoshi Kometani,Ming Zhong,Manish Mittal,Zhigang Hong,Thirumala‐Devi Kanneganti,Jalees Rehman,Asrar B. Malik
出处
期刊:Immunity
[Elsevier]
日期:2018-07-01
卷期号:49 (1): 56-65.e4
被引量:282
标识
DOI:10.1016/j.immuni.2018.04.032
摘要
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.
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