Abstract
gp34, which we had identified as a target molecule of the trans-activation by Tax of human T-cell leukemia virus type I (HTLV-I), has been found to bind OX40, a member of the tumor necrosis factor receptor family, resulting in growth stimulation of activated T cells. We here demonstrate that not only gp34 (OX40L), but also OX40 can be transcriptionally activated by Tax. Three Tax-producing human T-cell lines carrying the HTLV-I genome expressed OX40 on their surfaces. Furthermore, Tax-induced transcriptional activation of OX40 was shown in Tax-inducible JPX-9 cells. These results demonstrate that both OX40 and its ligand (gp34) are constitutively expressed on the surfaces of Tax-expressing T lymphocytes, suggesting that the OX40L/OX40 system contributes to growth stimulation of the virus-infected T cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cadmium / pharmacology
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Cadmium Chloride
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Chlorides / pharmacology
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Culture Media, Conditioned / pharmacology
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Gene Expression Regulation, Leukemic / drug effects
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Gene Expression Regulation, Viral* / drug effects
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Gene Products, tax / physiology*
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Human T-lymphotropic virus 1 / physiology*
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Humans
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Leukemia-Lymphoma, Adult T-Cell / pathology
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Membrane Glycoproteins*
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Neoplasm Proteins / biosynthesis
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Neoplasm Proteins / genetics
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OX40 Ligand
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Receptors, OX40
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Receptors, Tumor Necrosis Factor / biosynthesis*
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Receptors, Tumor Necrosis Factor / genetics
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T-Lymphocytes / metabolism
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T-Lymphocytes / virology*
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Transcriptional Activation*
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Tumor Cells, Cultured / drug effects
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Tumor Necrosis Factor Receptor Superfamily, Member 7 / biosynthesis*
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Tumor Necrosis Factor Receptor Superfamily, Member 7 / genetics
Substances
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Chlorides
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Culture Media, Conditioned
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Gene Products, tax
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Membrane Glycoproteins
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Neoplasm Proteins
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OX40 Ligand
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Receptors, OX40
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Receptors, Tumor Necrosis Factor
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TNFRSF4 protein, human
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TNFSF4 protein, human
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Tumor Necrosis Factor Receptor Superfamily, Member 7
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Cadmium
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Cadmium Chloride