Fermented Oyster Extract-induced Osteoblast Differentiation and Bone Formation by Activating the Wntβ-catenin Signaling Pathway

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dc.contributor.author Molagoda, I. M. N.
dc.contributor.author Jayasooriya, R. G. P. T.
dc.contributor.author Choi, Y. H.
dc.contributor.author Kim, G. Y.
dc.date.accessioned 2022-02-01T15:10:01Z
dc.date.available 2022-02-01T15:10:01Z
dc.date.issued 2021-12
dc.identifier.citation International Symposium of Rajarata University (ISYMRU 2021) en_US
dc.identifier.issn 2235-9710
dc.identifier.uri http://repository.rjt.ac.lk/handle/123456789/3414
dc.description.abstract The pacific oyster, Crassostrea gigas, is well-known as a nutritious food. Recently, we revealed that fermented extract of C. gigas (FO) inhibited ovariectomy-induced osteoporosis, resulting from suppression of osteoclastogenesis. However, since the beneficial effect of FO on osteogenesis is poorly understood, in this study it was examined in mouse preosteoblast MC3T3-E1 cells, human osteosarcoma MG-63 osteoblast-like cells, and zebrafish larvae. We found that FO increased mitochondrial activity from days 1 to 7; however, total cell number of MC3T3-E1 cells gradually decreased without any change in cell viability, which suggests that FO stimulates the differentiation of MC3T3-E1 cells. FO also promoted the expression of osteoblast marker genes, including runt-related transcription factor 2 (mRUNX2), alkaline phosphatase (mALP), collagen type I α1 (mCol1α1), osteocalcin (mOCN), osterix (mOSX), bone morphogenetic protein 2 (mBMP2), and mBMP4 in MC3T3-E1 cells accompanied by a significant increase in ALP activity. FO also increased nuclear translocation of RUNX2 and OSX transcription factors, ALP activity, and calcification in vitro along with the upregulated expression of osteoblast-specific marker proteins such as RUNX2, ALP, Col1α1, OCN, OSX, and BMP4. Additionally, FO enhanced bone mineralization (calcein intensity) in zebrafish larvae at 9 days post-fertilization comparable to that in the β-glycerophosphate (GP)-treated group. All the tested osteoblast marker genes, including zRUNX2a, zRUNX2b, zALP, zCol1a1, zOCN, zBMP2, and zBMP4, were also remarkably upregulated in the zebrafish larvae in response to FO. It also promoted tail fin regeneration in adult zebrafish as same as the GP-treated groups. Furthermore, not only FO positively regulate β-catenin expression and Wnt/β-catenin luciferase activity, but pretreatment with a Wnt/β-catenin inhibitor (FH535) also significantly decreased FO-mediated bone mineralization in zebrafish larvae, which indicates that FO-induced osteogenesis depends on the Wnt/β-catenin pathway. Altogether, the current study suggests that the supplemental intake of FO has a beneficial effect on osteogenesis. en_US
dc.language.iso en en_US
dc.publisher Faculty of Technology Rajarata University of Sri Lanka en_US
dc.subject Crassostrea gigas en_US
dc.subject oyster en_US
dc.subject bone formation en_US
dc.subject mineralization en_US
dc.subject Wnt/β-catenin en_US
dc.title Fermented Oyster Extract-induced Osteoblast Differentiation and Bone Formation by Activating the Wntβ-catenin Signaling Pathway en_US
dc.type Article en_US


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