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dc.contributor.authorHaase, HR
dc.contributor.authorIvanovski, S
dc.contributor.authorWaters, MJ
dc.contributor.authorBartold, PM
dc.date.accessioned2017-05-03T15:17:05Z
dc.date.available2017-05-03T15:17:05Z
dc.date.issued2003
dc.date.modified2009-03-02T06:52:08Z
dc.identifier.issn0022-3484
dc.identifier.urihttp://hdl.handle.net/10072/21578
dc.description.abstractBACKGROUND: Growth hormone (GH) is a potent regulator of bone formation. The proposed mechanism of GH action is through the stimulation of osteogenic precursor cell proliferation and, following clonal expansion of these cells, promotion of differentiation along the osteogenic lineage. OBJECTIVES: We tested this hypothesis by studying the effects of GH on primary cell populations of human periodontal ligament cells (PLC) and alveolar bone cells (ABC), which contain a spectrum of osteogenic precursors. METHODS: The cell populations were assessed for mineralization potential after long-term culture in media containing beta-glycerophosphate and ascorbic acid, by the demonstration of mineral deposition by Von Kossa staining. The proliferative response of the cells to GH was determined over a 48-h period using a crystal violet dye-binding assay. The profile of the cells in terms of osteogenic marker expression was established using quantitative reverse transcriptase polymerase chain reaction (RT-PCR) for alkaline phosphatase (ALP), osteopontin, osteocalcin, bone sialoprotein (BSP), as well as the bone morphogenetic proteins BMP-2, BMP-4 and BMP-7. RESULTS: As expected, a variety of responses were observed ranging from no mineralization in the PLC populations to dense mineralized deposition observed in one GH-treated ABC population. Over a 48-h period GH was found to be non-mitogenic for all cell populations. Quantitative reverse transcriptase polymerase chain reaction (RT-PCR) BSP mRNA expression correlated well with mineralizing potential of the cells. The change in the mRNA expression of the osteogenic markers was determined following GH treatment of the cells over a 48-h period. GH caused an increase in ALP in most cell populations, and also in BMP expression in some cell populations. However a decrease in BSP, osteocalcin and osteopontin expression in the more highly differentiated cell populations was observed in response to GH. CONCLUSION: The response of the cells indicates that while long-term treatment with GH may promote mineralization, short-term treatment does not promote proliferation of osteoblast precursors nor induce expression of late osteogenic markers.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoen_AU
dc.publisherBlackwell Munksgaard
dc.publisher.placeCopenhagen, Denmark
dc.relation.ispartofpagefrom366
dc.relation.ispartofpageto374
dc.relation.ispartofissue4
dc.relation.ispartofjournalJournal of periodontal research
dc.relation.ispartofvolume38
dc.subject.fieldofresearchDentistry
dc.subject.fieldofresearchcode1105
dc.titleGrowth hormone regulates osteogenic marker mRNA expression in human periodontal fibroblasts and alveolar bone-derived cells
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.date.issued2003
gro.hasfulltextNo Full Text
gro.griffith.authorIvanovski, Saso


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