Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Investigating the Role of FGF18 in the Cultivation and Osteogenic Differentiation of Mesenchymal Stem Cells

Full metadata record
DC Field Value Language
dc.contributor.authorJeon, Eunyi-
dc.contributor.authorYun, Ye-Rang-
dc.contributor.authorKang, Wonmo-
dc.contributor.authorLee, Sujin-
dc.contributor.authorKoh, Young-Hyag-
dc.contributor.authorKim, Hae-Won-
dc.contributor.authorSuh, Chang Kook-
dc.contributor.authorJang, Jun-Hyeog-
dc.date.accessioned2021-09-06T16:22:57Z-
dc.date.available2021-09-06T16:22:57Z-
dc.date.created2021-06-18-
dc.date.issued2012-08-24-
dc.identifier.issn1932-6203-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/107682-
dc.description.abstractFibroblast growth factor18 (FGF18) belongs to the FGF family and is a pleiotropic protein that stimulates proliferation in several tissues. Bone marrow mesenchymal stem cells (BMSCs) participate in the normal replacement of damaged cells and in disease healing processes within bone and the haematopoietic system. In this study, we constructed FGF18 and investigated its effects on rat BMSCs (rBMSCs). The proliferative effects of FGF18 on rBMSCs were examined using an MTS assay. To validate the osteogenic differentiation effects of FGF18, ALP and mineralization activity were examined as well as osteogenic differentiation-related gene levels. FGF18 significantly enhanced rBMSCs proliferation (p < 0.001) and induced the osteogenic differentiation by elevating ALP and mineralization activity of rBMSCs (p < 0.001). Furthermore, these osteogenic differentiation effects of FGF18 were confirmed via increasing the mRNA levels of collagen type I (Col I), bone morphogenetic protein 4 (BMP4), and Runt-related transcription factor 2 (Runx2) at 3 and 7 days. These results suggest that FGF18 could be used to improve bone repair and regeneration.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPUBLIC LIBRARY SCIENCE-
dc.subjectFIBROBLAST-GROWTH-FACTOR-
dc.subjectFACTOR (FGF)-18-
dc.subjectOSTEOBLAST-
dc.subjectPROLIFERATION-
dc.subjectFACTOR-18-
dc.subjectFGF-18-
dc.subjectEXPRESSION-
dc.subjectTHERAPY-
dc.subjectSIGNALS-
dc.subjectPROTEIN-
dc.titleInvestigating the Role of FGF18 in the Cultivation and Osteogenic Differentiation of Mesenchymal Stem Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKoh, Young-Hyag-
dc.identifier.doi10.1371/journal.pone.0043982-
dc.identifier.scopusid2-s2.0-84866607725-
dc.identifier.wosid000308225500132-
dc.identifier.bibliographicCitationPLOS ONE, v.7, no.8-
dc.relation.isPartOfPLOS ONE-
dc.citation.titlePLOS ONE-
dc.citation.volume7-
dc.citation.number8-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusFIBROBLAST-GROWTH-FACTOR-
dc.subject.keywordPlusFACTOR (FGF)-18-
dc.subject.keywordPlusOSTEOBLAST-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusFACTOR-18-
dc.subject.keywordPlusFGF-18-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusSIGNALS-
dc.subject.keywordPlusPROTEIN-
Files in This Item
There are no files associated with this item.
Appears in
Collections
Graduate School > Department of Bioengineering > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Koh, Young Hag photo

Koh, Young Hag
Department of Bioengineering
Read more

Altmetrics

Total Views & Downloads

BROWSE