A NOVEL MEMBER OF THE INTEGRIN RECEPTOR FAMILY MEDIATES ARG-GLY-ASP STIMULATED NEUTROPHIL PHAGOCYTOSIS
A NOVEL MEMBER OF THE INTEGRIN RECEPTOR FAMILY MEDIATES ARG-GLY-ASP STIMULATED NEUTROPHIL PHAGOCYTOSIS
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DOI:
10.1083/jcb.108.5.1935
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发表时间:
1989-05-01
影响因子:
7.8
通讯作者:
BROWN, EJ
中科院分区:
文献类型:
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作者:
GRESHAM, HD;GOODWIN, JL;BROWN, EJ
Human neutrophils (PMN) express a heterodimeric receptor that has ligand binding specificity for the Arg-Gly-Asp (RGD) sequence within many adhesive proteins. A monoclonal antibody, B6H12, which binds to this receptor, inhibits both RGD-mediated ligand binding and stimulation of IgG-mediated phagocytosis by fibronectin, fibrinogen, vitronectin, von Willebrand''s factor, and collagen type IV. By several criteria this receptor is neither a known very late antigen, a known cytoadhesin (gp IIb/IIIa-vitronectin receptor), nor a member of the LFA-1, Mac-1, p150,95 group of integrin receptors. Ligand binding via this receptor is rapidly inactivated by products of the myeloperoxidase-hydrogen peroxide-halide system of PMN. We conclude that this receptor, for which we propose the name leukocyte response integrin, is a signal-transducing molecule on PMN which may have a significant early role in modulation of PMN function at inflammatory sites.