4.8 Article

Amphiphysin IIm, a novel amphiphysin II isoform, is required for macrophage phagocytosis

Journal

IMMUNITY
Volume 12, Issue 3, Pages 285-292

Publisher

CELL PRESS
DOI: 10.1016/S1074-7613(00)80181-8

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Funding

  1. NIAID NIH HHS [AI-R37-25032, AI-R01-32972] Funding Source: Medline
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI032972, R37AI025032] Funding Source: NIH RePORTER

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Phagocytosis of pathogens by macrophages initiates the innate immune response, which in turn orchestrates the adaptive immune response. Amphiphysin II participates in receptor-mediated endocytosis, in part, by recruiting the GTPase dynamin to the nascent endosome. We demonstrate here that a novel isoform of amphiphysin II associates with early phagosomes in macrophages. We have ablated the dynamin-binding site of this protein and shown that this mutant form of amphiphysin II inhibits phagocytosis at the stage of membrane extension around the bound particles. We define a signaling cascade in which PI3K is required to recruit amphiphysin II to the phagosome, and amphiphysin II in turn recruits dynamin. Thus, amphiphysin II facilitates a critical initial step in host response to infection.

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