Publication:
Retroviral transduction of human periodontal cells with a temperature-sensitive SV40 large T antigen

dc.contributor.authorsParkar, MH; Kuru, L; O'Hare, M; Newman, HN; Hughes, F; Olsen, I
dc.date.accessioned2022-03-12T17:16:15Z
dc.date.accessioned2026-01-11T14:37:10Z
dc.date.available2022-03-12T17:16:15Z
dc.date.issued1999
dc.description.abstractThe periodontal ligament (PDL) is considered to contain subpopulations of cells responsible for the development, repair and regeneration of the periodontium. Cell cultures have been used as model systems in order to understand the complex cellular and biochemical events underlying these processes, In order to obtain long-term cultures of these cells that can be cloned and characterized, primary cultures of PDL and gingival cells were infected with an amphotropic retroviral construct encoding a temperature-sensitive SV40 large T antigen (tsT). After selection for drug resistance, the cells expressed the T antigen and proliferated at 34 degrees C for more than 40 passages. However, when the T antigen was inactivated by incubation at 39 degrees C, the cultures became growth-arrested and the granularity of the cells increased, possibly as a result of differentiation. Reverse transcribed-polymerase chain reaction and flow cytometry showed that the tsT-transduced cells expressed a number of soft and hard connective-tissue antigens, including osteocalcin, osteonectin, osteopontin, collagen type I and alkaline phosphatase. Moreover, incubation of the transduced PDL cells at 39 degrees C was found to upregulate the expression of osteocalcin, osteopontin and collagen type I, but downregulate osteonectin. At this temperature, the presence of the dexamethasone downregulated type I collagen, while vitamin D-3 had no effect on the expression of any of the antigens examined. Under all culture conditions, antigen expression was far higher in the transduced PDL cells than the gingival cells. The findings thus show that growth of the tsT-transduced PDL and gingival cells is temperature-dependent and that the presence of the T antigen increases their lifespan but does not ablate the expression of certain of their characteristic phenotypic and functional features. (C) 1999 Elsevier Science Ltd. All rights reserved.
dc.identifier.doi10.1016/S0003-9969(99)00077-1
dc.identifier.eissn1879-1506
dc.identifier.issn0003-9969
dc.identifier.pubmed10530915
dc.identifier.urihttps://hdl.handle.net/11424/227486
dc.identifier.wosWOS:000082754600006
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relation.ispartofARCHIVES OF ORAL BIOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectperiodontal cells
dc.subjectSV40 T antigen
dc.subjectHUMAN GINGIVAL FIBROBLASTS
dc.subjectOSTEOBLAST-LIKE CELLS
dc.subjectLARGE TUMOR-ANTIGEN
dc.subjectLIGAMENT CELLS
dc.subjectALKALINE-PHOSPHATASE
dc.subjectGENE-EXPRESSION
dc.subjectIN-VITRO
dc.subjectFLOW-CYTOMETRY
dc.subjectINVITRO
dc.subjectLINE
dc.titleRetroviral transduction of human periodontal cells with a temperature-sensitive SV40 large T antigen
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage834
oaire.citation.issue10
oaire.citation.startPage823
oaire.citation.titleARCHIVES OF ORAL BIOLOGY
oaire.citation.volume44

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