• Anke Di, Tomohiro Kiya, Haixia Gong, Xiaopei Gao, and Asrar B Malik.
• Department of Pharmacology and the Center for Lung and Vascular Biology, The University of Illinois College of Medicine, Chicago, IL 60612, USA.
• J. Cell. Sci. 2017 Feb 15; 130 (4): 735-744.

AbstractAcidification of macrophage phagosomes serves an important bactericidal function. We show here that the redox-sensitive transient receptor potential (TRP) cation channel TRPM2 is expressed in the phagosomal membrane and regulates macrophage bactericidal activity through the activation of phagosomal acidification. Measurement of the TRPM2 current in phagosomes identified TRPM2 as a functional redox-sensitive cation channel localized in the phagosomal membrane. Simultaneous measurements of phagosomal Ca(2+) changes and phagosome acidification in macrophages undergoing phagocytosis demonstrated that TRPM2 was required to mediate the efflux of cations and for phagosomal acidification during the process of phagosome maturation. Acidification in phagosomes was significantly reduced in macrophages isolated from Trpm2(-/-) mice as compared to wild type, and acidification was coupled to reduced bacterial clearance in Trpm2(-/-) mice. Trpm2(+/+) macrophages treated with the vacuolar H(+)-ATPase inhibitor bafilomycin showed reduced bacterial clearance, similar to that in Trpm2(-/-) macrophages. Direct activation of TRPM2 using adenosine diphosphate ribose (ADPR) induced both phagosomal acidification and bacterial killing. These data collectively demonstrate that TRPM2 regulates phagosomal acidification, and is essential for the bacterial killing function of macrophages.© 2017. Published by The Company of Biologists Ltd.

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