Abstract
CD45 is a high-molecular-weight transmembrane protein tyrosine phosphatase expressed only by nucleated cells of hematopoietic origin. To examine function, mouse CD8+ cytolytic T-cell clones were derived that had a specific defect in the expression of CD45. Northern (RNA) blot analysis indicates that the CD45 deficiency is due to either a transcriptional defect or mRNA instability. The CD45-deficient cells were greatly diminished in their ability to respond to antigen. All functional parameters of T-cell receptor signalling analyzed (cytolysis of targets, proliferation, and cytokine production) were markedly diminished. A CD45+ revertant was isolated, and the ability to respond to antigen was restored. These results support a central and immediate role for this transmembrane protein tyrosine phosphatase in T-cell receptor signalling.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antigens, CD / biosynthesis*
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Antigens, CD / metabolism
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Antigens, Differentiation, T-Lymphocyte*
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Blotting, Northern
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CD8 Antigens
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Cell Division
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Cell Line
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Clone Cells
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Female
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Flow Cytometry
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Histocompatibility Antigens / biosynthesis*
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Histocompatibility Antigens / metabolism
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Leukocyte Common Antigens
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Lymphokines / metabolism
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Mice
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Mice, Inbred CBA
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Mice, Inbred DBA
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Phosphoprotein Phosphatases / metabolism*
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Protein Tyrosine Phosphatases
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Receptors, Antigen, T-Cell / metabolism*
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Signal Transduction
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T-Lymphocytes, Cytotoxic / enzymology*
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T-Lymphocytes, Cytotoxic / immunology
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T-Lymphocytes, Cytotoxic / metabolism
Substances
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Antigens, CD
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Antigens, Differentiation, T-Lymphocyte
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CD8 Antigens
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Histocompatibility Antigens
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Lymphokines
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Receptors, Antigen, T-Cell
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Phosphoprotein Phosphatases
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Leukocyte Common Antigens
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Protein Tyrosine Phosphatases