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      Mediation by a CREB family transcription factor of NGF-dependent survival of sympathetic neurons.

      Science (New York, N.Y.)
      Animals, Apoptosis, Axons, drug effects, metabolism, Brain-Derived Neurotrophic Factor, pharmacology, Cell Nucleus, Cell Survival, Cells, Cultured, Cyclic AMP Response Element-Binding Protein, antagonists & inhibitors, Gene Expression Regulation, Genes, bcl-2, Genetic Vectors, Nerve Growth Factor, Neurons, cytology, PC12 Cells, Promoter Regions, Genetic, Proto-Oncogene Proteins c-bcl-2, genetics, Rats, Recombinant Fusion Proteins, Signal Transduction, Sympathetic Nervous System, Transfection

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          Abstract

          Nerve growth factor (NGF) and other neurotrophins support survival of neurons through processes that are incompletely understood. The transcription factor CREB is a critical mediator of NGF-dependent gene expression, but whether CREB family transcription factors regulate expression of genes that contribute to NGF-dependent survival of sympathetic neurons is unknown. CREB-mediated gene expression was both necessary for NGF-dependent survival and sufficient on its own to promote survival of sympathetic neurons. Moreover, expression of Bcl-2 was activated by NGF and other neurotrophins by a CREB-dependent transcriptional mechanism. Overexpression of Bcl-2 reduced the death-promoting effects of CREB inhibition. Together, these data support a model in which neurotrophins promote survival of neurons, in part through a mechanism involving CREB family transcription factor-dependent expression of genes encoding prosurvival factors.

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