SummaryPhagocytosis of large extracellular particles such as apoptotic bodies requires delivery of the intracellular endosomal and lysosomal membranes to form plasmalemmal pseudopods. Here, we identified mucolipin TRP channel 1 (TRPML1) as the key lysosomal Ca2+ channel regulating focal exocytosis and phagosome biogenesis. Both particle ingestion and lysosomal exocytosis are inhibited by synthetic TRPML1 blockers and are defective in macrophages isolated from TRPML1 knockout mice. Furthermore, TRPML1 overexpression and TRPML1 agonists facilitate both lysosomal exocytosis and particle uptake. Using time-lapse confocal imaging and direct patch clamping of phagosomal membranes, we found that particle binding induces lysosomal PI(3,5)P2 elevati...
B-lymphocytes possess a specialized lysosomal compartment, the regulated transformation of which has...
Mutations in TRPML1 cause the lysosomal storage disease mucolipidosis type IV (MLIV). The role of TR...
The lysosomal calcium channel TRPML1, whose mutations cause the lysosomal storage disorder (LSD) muc...
Macrophages participate in two main biological functions; they actively participate in apoptotic bod...
Abstract TRPML1 channel is a non-selective group-2 transient receptor potential (TRP) channel with C...
Both TRPML1 and TRPML3 are members of the mucolipin subfamily of Transient Receptor Potential (TRP) ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Transient receptor potential (TRP) mucolipins (TRPMLs), encoded by the MCOLN genes, are patho-physio...
AbstractThe mucolipin family of Transient Receptor Potential (TRPML) proteins is predicted to encode...
Membrane fusion and fi ssion events in intracellular traffi cking are controlled by both intralumina...
B-lymphocytes possess a specialized lysosomal compartment, the regulated transformation of which has...
B-lymphocytes possess a specialized lysosomal compartment, the regulated transformation of which has...
Mutations in TRPML1 cause the lysosomal storage disease mucolipidosis type IV (MLIV). The role of TR...
The lysosomal calcium channel TRPML1, whose mutations cause the lysosomal storage disorder (LSD) muc...
Macrophages participate in two main biological functions; they actively participate in apoptotic bod...
Abstract TRPML1 channel is a non-selective group-2 transient receptor potential (TRP) channel with C...
Both TRPML1 and TRPML3 are members of the mucolipin subfamily of Transient Receptor Potential (TRP) ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Macrophages clear invading pathogens by phagocytosis. Phagocytosis is a complex mechanism involving ...
Transient receptor potential (TRP) mucolipins (TRPMLs), encoded by the MCOLN genes, are patho-physio...
AbstractThe mucolipin family of Transient Receptor Potential (TRPML) proteins is predicted to encode...
Membrane fusion and fi ssion events in intracellular traffi cking are controlled by both intralumina...
B-lymphocytes possess a specialized lysosomal compartment, the regulated transformation of which has...
B-lymphocytes possess a specialized lysosomal compartment, the regulated transformation of which has...
Mutations in TRPML1 cause the lysosomal storage disease mucolipidosis type IV (MLIV). The role of TR...
The lysosomal calcium channel TRPML1, whose mutations cause the lysosomal storage disorder (LSD) muc...