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dc.contributor.authorGatto, Cheryl L.
dc.contributor.authorWalker, Barbara J.
dc.contributor.authorLambert, Stephen
dc.date2022-08-11T08:08:57.000
dc.date.accessioned2022-08-23T16:13:52Z
dc.date.available2022-08-23T16:13:52Z
dc.date.issued2003-08-06
dc.date.submitted2008-09-11
dc.identifier.citationJ Cell Biol. 2003 Aug 4;162(3):489-98. <a href="http://dx.doi.org/10.1083/jcb.200303039">Link to article on publisher's site</a>
dc.identifier.issn0021-9525 (Print)
dc.identifier.doi10.1083/jcb.200303039
dc.identifier.pmid12900397
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33725
dc.description.abstractNodes of Ranvier are specialized, highly polarized axonal domains crucial to the propagation of saltatory action potentials. In the peripheral nervous system, axo-glial cell contacts have been implicated in Schwann cell (SC) differentiation and formation of the nodes of Ranvier. SC microvilli establish axonal contact at mature nodes, and their components have been observed to localize early to sites of developing nodes. However, a role for these contacts in node formation remains controversial.Using a myelinating explant culture system, we have observed that SCs reorganize and polarize microvillar components, such as the ezrin-binding phosphoprotein 50 kD/regulatory cofactor of the sodium-hydrogen exchanger isoform 3 (NHERF-1), actin, and the activated ezrin, radixin, and moesin family proteins before myelination in response to inductive signals. These components are targeted to the SC distal tips where live cell imaging reveals novel, dynamic growth cone-like behavior. Furthermore, localized activation of the Rho signaling pathway at SC tips gives rise to these microvillar component-enriched "caps" and influences the efficiency of node formation.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12900397&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1083/jcb.200303039
dc.subjectActins; Animals; Animals, Newborn; Cell Communication; Cell Differentiation; Cell Membrane; Cells, Cultured; Cytoskeletal Proteins; Fetus; Ganglia, Spinal; Growth Cones; Neurons, Afferent; Organ Culture Techniques; Peripheral Nervous System; Phosphoproteins; Ranvier's Nodes; Rats; Rats, Wistar; Schwann Cells; Signal Transduction; Sodium-Hydrogen Antiporter; rho GTP-Binding Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleLocal ERM activation and dynamic growth cones at Schwann cell tips implicated in efficient formation of nodes of Ranvier
dc.typeJournal Article
dc.source.journaltitleThe Journal of cell biology
dc.source.volume162
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/388
dc.identifier.contextkey627225
html.description.abstract<p>Nodes of Ranvier are specialized, highly polarized axonal domains crucial to the propagation of saltatory action potentials. In the peripheral nervous system, axo-glial cell contacts have been implicated in Schwann cell (SC) differentiation and formation of the nodes of Ranvier. SC microvilli establish axonal contact at mature nodes, and their components have been observed to localize early to sites of developing nodes. However, a role for these contacts in node formation remains controversial.Using a myelinating explant culture system, we have observed that SCs reorganize and polarize microvillar components, such as the ezrin-binding phosphoprotein 50 kD/regulatory cofactor of the sodium-hydrogen exchanger isoform 3 (NHERF-1), actin, and the activated ezrin, radixin, and moesin family proteins before myelination in response to inductive signals. These components are targeted to the SC distal tips where live cell imaging reveals novel, dynamic growth cone-like behavior. Furthermore, localized activation of the Rho signaling pathway at SC tips gives rise to these microvillar component-enriched "caps" and influences the efficiency of node formation.</p>
dc.identifier.submissionpathgsbs_sp/388
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages489-98


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