Abstract
An IFN-gamma-inducible protein, IP-10, has previously been described to belong to a gene family of chemotactic and mitogenic proteins, associated with inflammation and proliferation. Biochemical characterization of this predicted protein has been pursued through the development of polyclonal monospecific antisera to recombinant protein and synthetic peptides. These reagents establish that the IP-10 protein is secreted from a variety of cells (endothelial, monocyte, fibroblast, and keratinocyte) in response to IFN-gamma. Posttranslational processing occurs in the biosynthesis of this protein, resulting in a 6-7-kD species, which may reflect COOH-terminal cleavage. Pulse-chase studies indicate that this processing is a rapid event in the primary cell lines studied, completed in the 30-min labeling period. A model is presented for the processing and secondary structure of this protein. In an accompanying study, Kaplan, et al. using these antisera, demonstrate that the IP-10 protein is associated, in vivo, with a delayed-type hypersensitivity response.
MeSH Terms
Amino Acid Sequence
Biological Products/biosynthesis,genetics
Cells, Cultured
Chromatography, High Pressure Liquid
Cytokines
Electrophoresis, Polyacrylamide Gel
Enzyme-Linked Immunosorbent Assay
Escherichia coli/genetics,metabolism
Humans
Immunity, Cellular
Injections, Intradermal
Interferon-gamma/pharmacology
Molecular Sequence Data
RNA/analysis
Chemicals
Biological Products
Cytokines
RNA
Interferon-gamma
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Luster A D
Dewitt Wallace Research Laboratory Memorial Sloan-Kettering Cancer Center, New York.
Ravetch J V
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