Anoctamin 6 mediates effects essential for innate immunity downstream of P2X₇ receptors in macrophages

摘要

Purinergic P2X₇ receptors ( P2X₇R ) are fundamental to innate immune response. In macrophages, transient stimulation of P2X₇R activates several transport mechanisms and induces the scrambling of phospholipids with subsequent membrane blebbing and apoptosis. These processes support phagocytosis and subsequent killing of phagocytosed bacteria. Here we demonstrate that the stimulation of P2X₇ receptors activates anoctamin 6 ( ANO6 , TMEM16F ), a protein that functions as Ca2+ dependent phospholipid scramblase and Ca2+-activated Cl? channel. Inhibition or knockdown of ANO6 attenuates ATP -induced cell shrinkage, cell migration and phospholipid scrambling. In mouse macrophages, Ano6 produces large ion currents by stimulation of P2X₇ receptors and contributes to ATP -induced membrane blebbing and apoptosis, which is largely reduced in macrophages from Ano6 ?/? mice. ANO6 supports bacterial phagocytosis and killing by mouse and human THP-1 macrophages. Our data demonstrate that anoctamin 6 is an essential component of the immune defense by macrophages.