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Rachael Z. Murray,Jason G. Kay,Daniele G. Sangermani,Jennifer L. Stow*
Membrane traffic in activated macrophages is required for twocritical events in innate immunity: proinflammatory cytokinesecretion and phagocytosis of pathogens. We found a joint traffickingpathway linking both actions, which may economize membrane transportand augment the immune response. Tumor necrosis factor (TNF)is trafficked from the Golgi to the recycling endosome (RE),where vesicle-associated membrane protein 3 mediates its deliveryto the cell surface at the site of phagocytic cup formation.Fusion of the RE at the cup simultaneously allows rapid releaseof TNF and expands the membrane for phagocytosis.
Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland 4072, Australia.
* To whom correspondence should be addressed. E-mail: j.stow{at}imb.uq.edu.au
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