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pubmed-article:9653188pubmed:abstractTextAxonal injury increases intracellular Ca2+ and cAMP and has been shown to induce gene expression, which is thought to be a key event for regeneration. Increases in intracellular Ca2+ and/or cAMP can alter gene expression via activation of a family of transcription factors that bind to and modulate the expression of CRE (Ca2+/cAMP response element) sequence-containing genes. We have used Aplysia motor neurons to examine the role of CRE-binding proteins in axonal regeneration after injury. We report that axonal injury increases the binding of proteins to a CRE sequence-containing probe. In addition, Western blot analysis revealed that the level of ApCREB2, a CRE sequence-binding repressor, was enhanced as a result of axonal injury. The sequestration of CRE-binding proteins by microinjection of CRE sequence-containing plasmids enhanced axon collateral formation (both number and length) as compared with control plasmid injections. These findings show that Ca2+/cAMP-mediated gene expression via CRE-binding transcription factors participates in the regeneration of motor neuron axons.lld:pubmed
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pubmed-article:9653188pubmed:authorpubmed-author:MooreA NANlld:pubmed
pubmed-article:9653188pubmed:authorpubmed-author:DashP KPKlld:pubmed
pubmed-article:9653188pubmed:authorpubmed-author:ThamM NMNlld:pubmed
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pubmed-article:9653188pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:9653188pubmed:articleTitleSequestration of cAMP response element-binding proteins by transcription factor decoys causes collateral elaboration of regenerating Aplysia motor neuron axons.lld:pubmed
pubmed-article:9653188pubmed:affiliationDepartment of Neurobiology and Anatomy, University of Texas-Houston Health Science Center, Houston, TX 77225, USA. pdash@nba19.med.uth.tmc.edulld:pubmed
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pubmed-article:9653188pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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