Abstract
Fas is an apoptosis-signaling receptor molecule on the surface of a number of cell types. Molecular cloning and nucleotide sequence analysis revealed a human Fas messenger RNA variant capable of encoding a soluble Fas molecule lacking the transmembrane domain because of the deletion of an exon encoding this region. The expression of soluble Fas was confirmed by flow cytometry and immunocytochemical analysis. Supernatants from cells transfected with the variant messenger RNA blocked apoptosis induced by the antibody to Fas. Levels of soluble Fas were elevated in patients with systemic lupus erythematosus, and mice injected with soluble Fas displayed autoimmune features.
Publication types
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Antibodies / immunology
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Antigens, Surface / chemistry
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Antigens, Surface / genetics
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Antigens, Surface / immunology
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Antigens, Surface / physiology*
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Apoptosis*
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Arthritis, Rheumatoid / blood
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Base Sequence
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Cell Line
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Cell Membrane / chemistry
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Humans
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Lupus Erythematosus, Systemic / blood
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Mice
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Molecular Sequence Data
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RNA, Messenger / genetics
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Solubility
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T-Lymphocyte Subsets / immunology
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Transfection
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fas Receptor
Substances
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Antibodies
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Antigens, Surface
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RNA, Messenger
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fas Receptor
Associated data
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GENBANK/X83490
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GENBANK/X83491
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GENBANK/X83492
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GENBANK/X83493