This item is licensed Korea Open Government License
dc.contributor.author
문성희
dc.contributor.author
김성환
dc.contributor.author
김익연
dc.date.accessioned
2019-08-28T07:42:05Z
dc.date.available
2019-08-28T07:42:05Z
dc.date.issued
2017-10-12
dc.identifier.issn
0253-6269
dc.identifier.uri
https://repository.kisti.re.kr/handle/10580/14638
dc.description.abstract
Bone morphogenetic protein 2 (BMP-2) has been used clinically to encourage bone regeneration; although, there can be major side effects with larger doses. Therefore, there is a need to identify new small molecules to potentiate the osteogenic action of BMP-2. In this study, we investigated the effect of mollugin on bone formation in murine bi-potential mesenchymal progenitor C2C12 cells by combination with BMP-2. We found mollugin could enhance the BMP-2-mediated osteoblast differentiation of C2C12 cells. This was accompanied by the induction of other osteogenic BMPs. We also found the enhancing potential of mollugin may involve activation of the p38-Smad1/5/8 signaling axis. Furthermore, mollugin promoted skeletal development in zebrafish. The combination of BMP-2 with small molecules, including mollugin, could minimize its clinical limitations, and these molecules might lead to the development of effective stem cell stimulants for bone regeneration and fracture healing.
dc.language
eng
dc.relation.ispartofseries
Archives of Pharmacal Research
dc.title
Mollugin enhances the osteogenic action of BMP-2 via the p-38-Smad signaling pathway