Abstract
In the mouse fibrosarcoma cell line L929sA, tumor necrosis factor (TNF) stimulates activation of the stress-responsive p38 mitogen-activated protein kinase (MAPK), as well as the classical p42 and p44 MAPK. TNF signaling can be mediated by p55 or p75 TNF receptors. Here, we demonstrate that TNF-R55 is sufficient to activate p42/p44 MAPK and p38 MAPK. Moreover, by expressing different membrane-bound or purely cytoplasmic truncations of TNF-R55, we show that the intracellular death domain of TNF-R55 is the crucial domain involved. The cytoplasmic membrane-proximal region of TNF-R55, known to induce neutral sphingomyelinase activation, is not required for activation of p38 MAPK or p421p44 MAPK.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Antigens, CD / chemistry
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Antigens, CD / physiology*
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Base Sequence
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Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
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DNA Primers
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Enzyme Activation
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Fibrosarcoma / enzymology
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Fibrosarcoma / pathology
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Mice
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Mitogen-Activated Protein Kinases*
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Molecular Sequence Data
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Receptors, Tumor Necrosis Factor / chemistry
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Receptors, Tumor Necrosis Factor / physiology*
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Receptors, Tumor Necrosis Factor, Type I
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Recombinant Proteins / metabolism
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Tumor Cells, Cultured
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Tumor Necrosis Factor-alpha / physiology*
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p38 Mitogen-Activated Protein Kinases
Substances
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Antigens, CD
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DNA Primers
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Receptors, Tumor Necrosis Factor
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Receptors, Tumor Necrosis Factor, Type I
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Recombinant Proteins
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Tumor Necrosis Factor-alpha
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Calcium-Calmodulin-Dependent Protein Kinases
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Mitogen-Activated Protein Kinases
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p38 Mitogen-Activated Protein Kinases