[PDF][PDF] The TWIK2 potassium efflux channel in macrophages mediates NLRP3 inflammasome-induced inflammation

A Di, S Xiong, Z Ye, RKS Malireddi, S Kometani… - Immunity, 2018 - cell.com
A Di, S Xiong, Z Ye, RKS Malireddi, S Kometani, M Zhong, M Mittal, Z Hong, TD Kanneganti
Immunity, 2018cell.com
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 (K 2P) 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 …
Summary
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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