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Expression patterns of neurotrophic factor mRNAs in developing human teeth

dc.contributor.authorOlson, Larsen_US
dc.contributor.authorSeiger, Åkeen_US
dc.contributor.authorNosrat, Irina V.en_US
dc.contributor.authorNosrat, Christopher A.en_US
dc.date.accessioned2006-09-08T20:09:42Z
dc.date.available2006-09-08T20:09:42Z
dc.date.issued2002-11en_US
dc.identifier.citationNosrat, Irina; Seiger, Åke; Olson, Lars; Nosrat, Christopher A.; (2002). "Expression patterns of neurotrophic factor mRNAs in developing human teeth." Cell and Tissue Research 310(2): 177-187. <http://hdl.handle.net/2027.42/42275>en_US
dc.identifier.issn0302-766Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42275
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12397373&dopt=citationen_US
dc.description.abstractNeurotrophic factors regulate survival, differentiation, growth and plasticity in the nervous system. In addition, based on their specific and shifting temporospatial expression patterns, neurotrophic factors have been implicated in morphogenetic events during tooth development in rodents. To determine whether these findings in rodents could be related to humans, we have now studied nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4), glial cell-line derived neurotrophic factor (GDNF), and neurturin (NTN) mRNA expression patterns in developing human teeth during gestational weeks 6.5–11. Using in situ hybridization histochemistry, we found distinct and specific patterns of neurotrophin and GDNF mRNA expression in the developing human teeth. NGF mRNA labeling was weak and confined predominantly to the dental papilla. BDNF mRNA labeling was stronger than NGF mRNA and was seen in the mesenchyme located lateral to the dental organ, as well as in epithelial structures (inner dental epithelium and enamel knot). NT-3 mRNA was observed in the dental papilla and in the area of the cervical loop. NT-4 mRNA was expressed in both oral and dental epithelia in all stages studied. GDNF mRNA was found in the dental follicle and at different sites in the inner dental epithelium. Weak NTN mRNA labeling was also found in the developing teeth. Based on these findings, we suggest that neurotrophins, GDNF and NTN might be involved in morphogenetic events during early stages of tooth development in humans. Protein gene product (PGP) 9.5-immunoreactive nerve fibers were observed in the dental follicle by 11 weeks coinciding with the labeling for neurotrophic factor mRNAs in this structure. This suggests that these neurotrophic factors might be involved in the innervation of dental structures. The rich expression of neurotrophic factors in developing dental tissues suggests that developing, or possibly adult, dental tissue might be used as an allograft source of trophic support for diseases of the nervous system.en_US
dc.format.extent789335 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherLegacyen_US
dc.subject.otherNeurotrophin Development Tooth Differentiation Odontogenesis Epithelial-mesenchymal Interactions Humanen_US
dc.titleExpression patterns of neurotrophic factor mRNAs in developing human teethen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumLaboratory of Oral Neurobiology, BMS, University of Michigan Dental School, Ann Arbor, MI 48109-1078, USA,en_US
dc.contributor.affiliationumLaboratory of Oral Neurobiology, BMS, University of Michigan Dental School, Ann Arbor, MI 48109-1078, USA,en_US
dc.contributor.affiliationotherDepartment of Neuroscience, Karolinska Institutet, 171 77 Stockholm, Sweden,en_US
dc.contributor.affiliationotherDepartment of Clinical Neuroscience and Family Medicine, Karolinska Institutet, 14186 Huddinge, Sweden,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12397373en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42275/1/s00441-002-0618-8.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00441-002-0618-8en_US
dc.identifier.sourceCell and Tissue Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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