Scinovex
articleTop 10% cited

F4/80, a monoclonal antibody directed specifically against the mouse macrophage

European Journal of Immunology · 1981 · Vol. 11(10) · pp. 805–815
Jonathan M. AustynSiamon Gordon

Abstract

A hybridoma clone which secretes a macrophage (M phi)-specific monoclonal antibody, F4/80, was produced by fusing spleen cells from a rat hyperimmunized with cultured thioglycollate-induced mouse peritoneal M phi with a mouse myeloma, NS1. Binding of antibody to primary cells and cell lines was detected by radioimmune indirect binding assay, autoradiography or fluorescence-activated cell sorter analysis. F4/80 binds to mouse M phi from the peritoneal cavity or other sources, blood monocytes, M phi derived from bone marrow precursors in culture and M phi-like cell lines, but not to other cells, including polymorphonuclear leukocytes, lymphocytes or fibroblasts. F4/80 does not bind to M phi via Fc receptors, is not cytotoxic and is of the rat IgG2b subclass. Since F4/80 binds to all M phi defined by adherence, morphology and immune phagocytosis, it provides a new marker to define the M phi in the mouse. Large differences in expression of antigen F4/80 were found, depending on intraperitoneal stimulation, time in culture and stage of maturation. Immunoprecipitation experiments demonstrated that the antigen F4/80 is part of a component of Mr 160000 which is synthesized by the M phi and, at least in part, exposed on the cell surface.

Monoclonal and Polyclonal Antibodies ResearchComplement system in diseasesGalectins and Cancer BiologyBiologyMolecular biologyMonoclonal antibodyAntigenPeritoneal cavityCytotoxic T cellAntibodyclone (Java method)MacrophageSpleen

MeSH terms

AnimalsAntibodies, MonoclonalAntibody SpecificityAntigensAutoradiographyBinding Sites, AntibodyCell LineCell SeparationFemaleFlow CytometryGuinea PigsMacrophagesMaleMice, Inbred C57BLMice, Inbred Strains
Citations
1,604
FWCI
12.64
field-weighted impact
References
39
Percentile
99%
vs. same field & year
Citations per year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.