Abstract
Overexpression of gp120, the major coat protein of the HIV-1 virus, in central glial cells, or treatment of neurons with gp120 in culture, produces apoptotic neuronal death. Here we demonstrate that CEP-1347 (KT7515), an inhibitor of mixed lineage kinase 3 (MLK3), an upstream activator of JNK, inhibits gp120IIIB-induced apoptosis of hippocampal neurons. Furthermore, expression of wild type MLK3 in hippocampal pyramidal neurons enhanced gp120IIIB-induced neurotoxicity, whereas expression of a dominant negative MLK3 protected neurons from the toxic effects of the glycoprotein. These results indicate a role for MLK3 signaling in gp120IIIB-induced neuronal death, and suggest potential clinical utility of CEP-1347 in inhibiting the progression of AIDS dementia.
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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Apoptosis / drug effects
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CD4 Antigens / pharmacology
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Carbazoles / pharmacology
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Cells, Cultured
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Coculture Techniques
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Culture Media, Conditioned / pharmacology
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Dose-Response Relationship, Drug
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Enzyme Activation / drug effects
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Enzyme Inhibitors / pharmacology
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Genes, Dominant
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HIV Envelope Protein gp120 / toxicity*
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HIV-1*
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Hippocampus
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Indoles / pharmacology
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MAP Kinase Kinase Kinases / antagonists & inhibitors
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MAP Kinase Kinase Kinases / genetics
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MAP Kinase Kinase Kinases / metabolism*
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Membrane Potentials / drug effects
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Mitochondria / drug effects
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Mitogen-Activated Protein Kinase Kinase Kinase 11
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Neuroglia / cytology
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Neurons / cytology
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Neurons / drug effects*
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Neurons / metabolism*
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Neuroprotective Agents
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Pyramidal Cells / cytology
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Pyramidal Cells / drug effects
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Pyramidal Cells / metabolism
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Rats
Substances
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CD4 Antigens
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Carbazoles
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Culture Media, Conditioned
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Enzyme Inhibitors
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HIV Envelope Protein gp120
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Indoles
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Neuroprotective Agents
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3,9-bis((ethylthio)methyl)-K-252a
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MAP Kinase Kinase Kinases