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dc.contributor.authorMelloni, Richard H.
dc.contributor.authorApostolides, Paul J.
dc.contributor.authorHamos, James E.
dc.contributor.authorDeGennaro, Louis J.
dc.date2022-08-11T08:09:01.000
dc.date.accessioned2022-08-23T16:15:52Z
dc.date.available2022-08-23T16:15:52Z
dc.date.issued1994-02-01
dc.date.submitted2008-11-21
dc.identifier.citationNeuroscience. 1994 Feb;58(4):683-703.
dc.identifier.issn0306-4522 (Print)
dc.identifier.pmid7514766
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34193
dc.description.abstractSynapse development and injury-induced reorganization have been extensively characterized morphologically, yet relatively little is known about the underlying molecular and biochemical events. To examine molecular mechanisms of synaptic development and rearrangement, we looked at the developmental pattern of expression of the neuron-specific gene synapsin I in granule cell neurons of the dentate gyrus and their accompanying mossy fibers during the main period of synaptogenic differentiation in the rat hippocampus. We found a significant difference between the temporal expression of synapsin I messenger RNA in dentate granule somata and the appearance of protein in their mossy fiber terminals during the postnatal development of these neurons. Next, to investigate the regulation of neuron-specific gene expression during the restoration of synaptic contacts in the central nervous system, we examined the expression of the synapsin I gene following lesions of hippocampal circuitry. These studies show marked changes in the pattern and intensity of synapsin I immunoreactivity in the dendritic fields of dentate granule cell neurons following perforant pathway transection. In contrast, changes in synapsin I messenger RNA expression in target neurons, and in those neurons responsible for the reinnervation of this region of the hippocampus, were not found to accompany new synapse formation. On a molecular level, both developmental and lesion data suggest that the expression of the synapsin I gene is tightly regulated in the central nervous system, and that considerable changes in synapsin I protein may occur in neurons without concomitant changes in the levels of its messenger RNA. Finally, our results suggest that the appearance of detectable levels of synapsin I protein in in developing and sprouting synapses coincides with the acquisition of function by those central synapses.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7514766&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/0306-4522(94)90448-0
dc.subjectAcetylcholinesterase; Animals; Animals, Newborn; Blotting, Western; DNA Probes; Denervation; Gene Expression Regulation; Hippocampus; Image Processing, Computer-Assisted; Immunohistochemistry; In Situ Hybridization; Male; RNA; RNA, Messenger; Rats; Rats, Sprague-Dawley; Synapses; Synapsins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleDynamics of synapsin I gene expression during the establishment and restoration of functional synapses in the rat hippocampus
dc.typeJournal Article
dc.source.journaltitleNeuroscience
dc.source.volume58
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/850
dc.identifier.contextkey670506
html.description.abstract<p>Synapse development and injury-induced reorganization have been extensively characterized morphologically, yet relatively little is known about the underlying molecular and biochemical events. To examine molecular mechanisms of synaptic development and rearrangement, we looked at the developmental pattern of expression of the neuron-specific gene synapsin I in granule cell neurons of the dentate gyrus and their accompanying mossy fibers during the main period of synaptogenic differentiation in the rat hippocampus. We found a significant difference between the temporal expression of synapsin I messenger RNA in dentate granule somata and the appearance of protein in their mossy fiber terminals during the postnatal development of these neurons. Next, to investigate the regulation of neuron-specific gene expression during the restoration of synaptic contacts in the central nervous system, we examined the expression of the synapsin I gene following lesions of hippocampal circuitry. These studies show marked changes in the pattern and intensity of synapsin I immunoreactivity in the dendritic fields of dentate granule cell neurons following perforant pathway transection. In contrast, changes in synapsin I messenger RNA expression in target neurons, and in those neurons responsible for the reinnervation of this region of the hippocampus, were not found to accompany new synapse formation. On a molecular level, both developmental and lesion data suggest that the expression of the synapsin I gene is tightly regulated in the central nervous system, and that considerable changes in synapsin I protein may occur in neurons without concomitant changes in the levels of its messenger RNA. Finally, our results suggest that the appearance of detectable levels of synapsin I protein in in developing and sprouting synapses coincides with the acquisition of function by those central synapses.</p>
dc.identifier.submissionpathgsbs_sp/850
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentDepartment of Neurology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages683-703


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