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hal.structure.identifierDepartment of Anatomy and Cell Biology
hal.structure.identifierRoudebush Veterans Administration Medical Center Indiana
dc.contributor.authorPLOTKIN, Lilian
hal.structure.identifierDepartment of Anatomy and Cell Biology
dc.contributor.authorLAIRD, Dale
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorAMÉDÉE, Joëlle
dc.date.accessioned2021-06-10T07:05:47Z
dc.date.available2021-06-10T07:05:47Z
dc.date.issued2016-05
dc.identifier.issn1471-2121
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/79042
dc.description.abstractEnElectron micrographs revealed the presence of gap junctions in osteoblastic cells over 40 years ago. These intercellular channels formed from connexins are present in bone forming osteoblasts, bone resorbing osteoclasts, and osteocytes (mature osteoblasts embedded in the mineralized bone matrix). More recently, genetic and pharmacologic studies revealed the role of connexins, and in particular Cx43, in the differentiation and function of all bone types. Furthermore, mutations in the gene encoding Cx43 were found to be causally linked to oculodentodigital dysplasia, a condition that results in an abnormal skeleton. Pannexins, molecules with similar structure and single-membrane channel forming potential as connexins when organized as hemichannels, are also expressed in osteoblastic cells. The function of pannexins in bone and cartilage is beginning to be uncovered, but more research is needed to determine the role of pannexins in bone development, adult bone mass and skeletal homeostasis. We describe here the current knowledge on the role of connexins and pannexins on skeletal health and disease.
dc.language.isoen
dc.publisherBioMed Central
dc.title.enRole of connexins and pannexins during ontogeny, regeneration, and pathologies of bone
dc.typeArticle de revue
dc.identifier.doi10.1186/s12860-016-0088-6
dc.subject.halSciences du Vivant [q-bio]
bordeaux.journalBMC Cell Biology
bordeaux.page19
bordeaux.volume17
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - U1026*
bordeaux.issueSuppl 1
bordeaux.institutionCNRS
bordeaux.institutionINSERM
bordeaux.institutionCHU de Bordeaux
bordeaux.institutionInstitut Bergonié
bordeaux.peerReviewedoui
hal.identifierinserm-01322569
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//inserm-01322569v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=BMC%20Cell%20Biology&rft.date=2016-05&rft.volume=17&rft.issue=Suppl%201&rft.spage=19&rft.epage=19&rft.eissn=1471-2121&rft.issn=1471-2121&rft.au=PLOTKIN,%20Lilian&LAIRD,%20Dale&AM%C3%89D%C3%89E,%20Jo%C3%ABlle&rft.genre=article


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