Phagocytosis involves the receptor-mediated extension of plasmalemmal protrusions, called pseudopods, which fuse at their tip to engulf a particle. Actin polymerizes under the nascent phagosome and may propel the protrusion of pseudopods. Alternatively, membrane extension could result from the localized insertion of intracellular membranes into the plasmalemma next to the particle. Here we show focal accumulation of VAMP3-containing vesicles, likely derived from recycling endosomes, in the vicinity of the nascent phagosome. Using green fluorescent protein (GFP) as both a fluorescent indicator and an exofacial epitope tag, we show that polarized fusion of VAMP3 vesicles precedes phagosome sealing. It is therefore likely that targeted delivery of endomembranes contributes to the elongation of pseudopods. In addition to mediating pseudopod formation, receptor-triggered focal secretion of endosomes may contribute to polarized membrane extension in processes such as lamellipodial elongation or chemotaxis.
Focal Exocytosis of Vamp3-Containing Vesicles at Sites of Phagosome Formation
Abbreviations used in this paper: CHO-IIA, Chinese hamster ovary cells stably transfected with FcγRIIA receptors; EEA1, early endosome-associated antigen-1; FcγR, opsonin receptor that recognizes the Fc domain of immunoglobulin G; GFP, green fluorescent protein; ITAM, immunoreceptor tyrosine activation motif; LAMP1, lysosome-associated membrane protein 1; PM-GFP, membrane-targeted form of GFP; RBC-Ig, rabbit IgG-opsonized sheep RBC; TeTx, tetanus toxin; VAMP-Ig, chimera of VAMP3 and the constant region of the human IgG heavy chain.
Lydia Bajno, Xiao-Rong Peng, Alan D. Schreiber, Hsiao-Ping Moore, William S. Trimble, Sergio Grinstein; Focal Exocytosis of Vamp3-Containing Vesicles at Sites of Phagosome Formation. J Cell Biol 1 May 2000; 149 (3): 697–706. doi: https://doi.org/10.1083/jcb.149.3.697
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