Efferocytosis requires periphagosomal Ca2+-signaling and TRPM7-mediated electrical activity

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Michael S. Schappe
Marta E. Stremska
Gregory W. Busey
Taylor K. Downs
Philip V. Seegren
Suresh K. Mendu
Zachary Flegal
Catherine A. Doyle
Eric J. Stipes
Bimal N. Desai
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[1] University of Virginia,Pharmacology Department
[2] University of Virginia,Carter Immunology Center
[3] University of Virginia,Robert M. Berne Cardiovascular Research Center
[4] Harvard Medical School,Department of Cell Biology
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Efficient clearance of apoptotic cells by phagocytosis, also known as efferocytosis, is fundamental to developmental biology, organ physiology, and immunology. Macrophages use multiple mechanisms to detect and engulf apoptotic cells, but the signaling pathways that regulate the digestion of the apoptotic cell cargo, such as the dynamic Ca2+ signals, are poorly understood. Using an siRNA screen, we identify TRPM7 as a Ca2+-conducting ion channel essential for phagosome maturation during efferocytosis. Trpm7-targeted macrophages fail to fully acidify or digest their phagosomal cargo in the absence of TRPM7. Through perforated patch electrophysiology, we demonstrate that TRPM7 mediates a pH-activated cationic current necessary to sustain phagosomal acidification. Using mice expressing a genetically-encoded Ca2+ sensor, we observe that phagosome maturation requires peri-phagosomal Ca2+-signals dependent on TRPM7. Overall, we reveal TRPM7 as a central regulator of phagosome maturation during macrophage efferocytosis.
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