期刊
JOURNAL OF CELL BIOLOGY
卷 174, 期 7, 页码 997-1007出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.200605004
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- NCI NIH HHS [R01CA098727, R01 CA098727] Funding Source: Medline
- NIAID NIH HHS [R37AI34867, R37 AI034867] Funding Source: Medline
- NIGMS NIH HHS [R01 GM064625, GM56827, R01 GM056827, R01GM064625] Funding Source: Medline
- NIMH NIH HHS [R01 MH061876, MH61876] Funding Source: Medline
Synaptotagmin (Syt) VII is a ubiquitously expressed member of the Syt family of Ca2+ sensors. It is present on lysosomes in several cell types, where it regulates Ca2+-dependent exocytosis. Because [Ca2+](i) and exocytosis have been associated with phagocytosis, we investigated the phagocytic ability of macrophages from Syt VII-/- mice. Syt VII-/- macrophages phagocytose normally at low particle/cell ratios but show a progressive inhibition in particle uptake under high load conditions. Complementation with Syt VII rescues this phenotype, but only when functional Ca2+-binding sites are retained. Reinforcing a role for Syt VII in Ca2+-dependent phagocytosis, particle uptake in Syt VII-/- macrophages is significantly less dependent on [Ca2+](i). Syt VII is concentrated on peripheral domains of lysosomal compartments, from where it is recruited to nascent phagosomes. Syt VII recruitment is rapidly followed by the delivery of Lamp1 to phagosomes, a process that is inhibited in Syt VII-/- macrophages. Thus, Syt VII regulates the Ca2+-dependent mobilization of lysosomes as a supplemental source of membrane during phagocytosis.
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