Czibener Cecilia, Sherer Nathan M, Becker Steven M, Pypaert Marc, Hui Enfu, Chapman Edwin R, Mothes Walther, Andrews Norma W
Section of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06510, USA.
J Cell Biol. 2006 Sep 25;174(7):997-1007. doi: 10.1083/jcb.200605004. Epub 2006 Sep 18.
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.
突触结合蛋白(Syt)VII是Ca2+传感器Syt家族中一种广泛表达的成员。它存在于多种细胞类型的溶酶体上,在那里调节Ca2+依赖性胞吐作用。由于细胞内Ca2+浓度([Ca2+]i)和胞吐作用与吞噬作用相关,我们研究了Syt VII基因敲除小鼠巨噬细胞的吞噬能力。Syt VII基因敲除的巨噬细胞在低颗粒/细胞比例下正常吞噬,但在高负荷条件下颗粒摄取呈现逐渐抑制。用Syt VII进行互补可挽救此表型,但仅当功能性Ca2+结合位点得以保留时。强化了Syt VII在Ca2+依赖性吞噬作用中的作用,Syt VII基因敲除巨噬细胞中的颗粒摄取对[Ca2+]i的依赖性显著降低。Syt VII集中在溶酶体区室的外周结构域,从那里它被招募到新生吞噬体。Syt VII的招募迅速伴随着溶酶体相关膜蛋白1(Lamp1)递送至吞噬体,这一过程在Syt VII基因敲除的巨噬细胞中受到抑制。因此,Syt VII在吞噬作用期间调节溶酶体的Ca2+依赖性动员,作为膜的补充来源。