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Phagocytosis is initiated by lateral clustering of receptors, which in turn activates Src-family kinases (SFKs). Activation of SFKs requires depletion of tyrosine phosphatases from the area of particle engagement. We investigated how the major phosphatase CD45 is excluded from contact sites, using single-molecule tracking. The mobility of CD45 increased markedly upon engagement of Fcγ receptors. While individual CD45 molecules moved randomly, they were displaced from the advancing phagocytic cup by an expanding diffusional barrier. By micropatterning IgG, the ligand of Fcγ receptors, we found that the barrier extended well beyond the perimeter of the receptor-ligand engagement zone. Second messengers generated by Fcγ receptors activated integrins, which formed an actin-tethered diffusion barrier that excluded CD45. The expanding integrin wave facilitates the zippering of Fcγ receptors onto the target and integrates the information from sparse receptor-ligand complexes, coordinating the progression and ultimate closure of the phagocytic cup.

Original publication

DOI

10.1016/j.cell.2015.11.048

Type

Journal article

Journal

Cell

Publication Date

14/01/2016

Volume

164

Pages

128 - 140

Keywords

Actins, Animals, Antigens, CD45, Humans, Integrins, Macrophages, Mice, Phagocytosis, Podosomes, Protein Structure, Tertiary, Receptor-Like Protein Tyrosine Phosphatases, Class 3, Receptors, IgG