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Conference Paper: Lipopolysaccharide differentially affects osteogenesis of healthy and inflammatory periodontium

TitleLipopolysaccharide differentially affects osteogenesis of healthy and inflammatory periodontium
Authors
Issue Date2019
PublisherInternational Association for Dental Research. The Journal's web site is located at http://www.iadr.org/
Citation
The 97th General Session of the International Association of Dental Research (IADR) held with the 48th Annual Meeting of the American Association for Dental Research (AADR) & the 43rd Annual Meeting of the Canadian Association for Dental Research (CADR), Vancouver, BC, Canada, 19-22 June 2019. In Journal of Dental Research, 2019, v. 98 n. Spec Iss A, abstract no. 2171 How to Cite?
AbstractObjectives: The aim of this study was to compare the proliferation and osteogenic capacities of human periodontal ligament stem cells (PDLSC) from healthy and inflammatory periodontal tissues, and to investigate the influence of P. gingivalis lipopolysaccharide (LPS) on them. Methods: Human PDL stem cells (PDLSC) were isolated from root-attached healthy (PDLSC-h), and inflammatory (PDLSC-i) periodontal tissue from healthy orthodontic (n=4), and ongoing periodontitis (n=4) patients. The PDLSCs were characterized by flow cytometry, and then challenged by P. gingivalis LPS (0.1, 1, 10 μg/ml). Their proliferative potentials and osteogenic differentiation capacities were evaluated and compared. Results: Both groups of PDLSCs exhibited similar mesenchymal stem cell surface markers. The proliferative rates of PDLSC-h were higher than PDLSC-i, both of which were not affected by LPS challenge. Upon 7 days of LPS challenge, there were increasing trends in expression levels of osteogenic markers (ALP, COL1, RUNX2 and OCN): the PDLSC-h peaked at 1 μg/ml LPS challenge, while PDLSC-i peaked at 0.1 μg/ml. However, after 14 days of LPS challenge, decreased expressions of osteogenic markers were detected upon 10 μg/ml LPS challenge in both groups of PDLSCs, with no significant difference among 0, 0.1 and 1 μg/ml LPS challenge. Generally, the osteogenic capacity of PDLSC-i was lower than PDLSC-h, with less expression of osteogenic markers and decreased Alizarin Red S staining. Conclusions: The osteogenic differentiation potential was lower in inflammatory periodontal tissue, and PDLSCs from healthy and periodontitis donors respond to LPS in different manners.
DescriptionPoster Session: Periodontal Research: Pathogenesis II - Final Presentation ID: 2171
Persistent Identifierhttp://hdl.handle.net/10722/273027

 

DC FieldValueLanguage
dc.contributor.authorLin, Y-
dc.contributor.authorJin, L-
dc.contributor.authorYang, Y-
dc.date.accessioned2019-08-06T09:21:10Z-
dc.date.available2019-08-06T09:21:10Z-
dc.date.issued2019-
dc.identifier.citationThe 97th General Session of the International Association of Dental Research (IADR) held with the 48th Annual Meeting of the American Association for Dental Research (AADR) & the 43rd Annual Meeting of the Canadian Association for Dental Research (CADR), Vancouver, BC, Canada, 19-22 June 2019. In Journal of Dental Research, 2019, v. 98 n. Spec Iss A, abstract no. 2171-
dc.identifier.urihttp://hdl.handle.net/10722/273027-
dc.descriptionPoster Session: Periodontal Research: Pathogenesis II - Final Presentation ID: 2171-
dc.description.abstractObjectives: The aim of this study was to compare the proliferation and osteogenic capacities of human periodontal ligament stem cells (PDLSC) from healthy and inflammatory periodontal tissues, and to investigate the influence of P. gingivalis lipopolysaccharide (LPS) on them. Methods: Human PDL stem cells (PDLSC) were isolated from root-attached healthy (PDLSC-h), and inflammatory (PDLSC-i) periodontal tissue from healthy orthodontic (n=4), and ongoing periodontitis (n=4) patients. The PDLSCs were characterized by flow cytometry, and then challenged by P. gingivalis LPS (0.1, 1, 10 μg/ml). Their proliferative potentials and osteogenic differentiation capacities were evaluated and compared. Results: Both groups of PDLSCs exhibited similar mesenchymal stem cell surface markers. The proliferative rates of PDLSC-h were higher than PDLSC-i, both of which were not affected by LPS challenge. Upon 7 days of LPS challenge, there were increasing trends in expression levels of osteogenic markers (ALP, COL1, RUNX2 and OCN): the PDLSC-h peaked at 1 μg/ml LPS challenge, while PDLSC-i peaked at 0.1 μg/ml. However, after 14 days of LPS challenge, decreased expressions of osteogenic markers were detected upon 10 μg/ml LPS challenge in both groups of PDLSCs, with no significant difference among 0, 0.1 and 1 μg/ml LPS challenge. Generally, the osteogenic capacity of PDLSC-i was lower than PDLSC-h, with less expression of osteogenic markers and decreased Alizarin Red S staining. Conclusions: The osteogenic differentiation potential was lower in inflammatory periodontal tissue, and PDLSCs from healthy and periodontitis donors respond to LPS in different manners.-
dc.languageeng-
dc.publisherInternational Association for Dental Research. The Journal's web site is located at http://www.iadr.org/-
dc.relation.ispartofJournal of Dental Research (Spec Issue)-
dc.relation.ispartofIADR/AADR/CADR 2019 General Session & Exhibition-
dc.titleLipopolysaccharide differentially affects osteogenesis of healthy and inflammatory periodontium-
dc.typeConference_Paper-
dc.identifier.emailJin, L: ljjin@hkucc.hku.hk-
dc.identifier.emailYang, Y: yangyanq@hku.hk-
dc.identifier.authorityJin, L=rp00028-
dc.identifier.authorityYang, Y=rp00045-
dc.identifier.hkuros299751-
dc.identifier.hkuros304564-
dc.identifier.volume98-
dc.identifier.issueSpec Iss A-
dc.identifier.spageabstract no. 2171-
dc.identifier.epageabstract no. 2171-
dc.publisher.placeUnited States-

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