传出细胞增多
TRPM7型
吞噬体
细胞生物学
吞噬作用
巨噬细胞
细胞凋亡
生物
瞬时受体电位通道
体外
受体
生物化学
作者
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
标识
DOI:10.1038/s41467-022-30959-4
摘要
Abstract 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 Ca 2+ signals, are poorly understood. Using an siRNA screen, we identify TRPM7 as a Ca 2+ -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 Ca 2+ sensor, we observe that phagosome maturation requires peri-phagosomal Ca 2+ -signals dependent on TRPM7. Overall, we reveal TRPM7 as a central regulator of phagosome maturation during macrophage efferocytosis.
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