Fermented Oyster Extract Promotes Osteoblast Differentiation by Activating the Wnt/β-Catenin Signaling Pathway, Leading to Bone Formation

被引:44
作者
Molagoda, Ilandarage Menu Neelaka [1 ]
Karunarathne, Wisurumuni Arachchilage Hasitha Maduranga [1 ]
Choi, Yung Hyun [2 ]
Park, Eui Kyun [3 ]
Jeon, You-Jin [1 ]
Lee, Bae-Jin [4 ]
Kang, Chang-Hee [5 ]
Kim, Gi-Young [1 ]
机构
[1] Jeju Natl Univ, Dept Marine Life Sci, Jeju 63243, South Korea
[2] Dong Eui Univ, Dept Biochem, Coll Oriental Med, Busan 47227, South Korea
[3] Kyungpook Natl Univ, Sch Dent, Inst Hard Tissue & Biotooth Regenerat, Dept Oral Pathol & Regenerat Med, Daegu 41940, South Korea
[4] Marine Bioproc Co Ltd, Busan 46048, South Korea
[5] Nakdonggang Natl Inst Biol Resources, Bioresources Industrializat Support Dept, Sangju 37242, South Korea
关键词
Crassostrea gigas; oyster; bone formation; mineralization; Wnt/beta-catenin; PEPTIDE; PURIFICATION; OSTEOPOROSIS; METABOLISM; OSTERIX; ACID;
D O I
10.3390/biom9110711
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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, it was examined in mouse preosteoblast MC3T3-E1 cells, human osteosarcoma MG-63 osteoblast-like cells, and zebrafish larvae in this study. 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 alpha 1 (mCol1 alpha 1), 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, Col1 alpha 1, OCN, OSX, and BMP4. Additionally, FO enhanced bone mineralization (calcein intensity) in zebrafish larvae at 9 days post-fertilization comparable to that in the beta-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 beta-catenin expression and Wnt/beta-catenin luciferase activity, but pretreatment with a Wnt/beta-catenin inhibitor (FH535) also significantly decreased FO-mediated bone mineralization in zebrafish larvae, which indicates that FO-induced osteogenesis depends on the Wnt/beta-catenin pathway. Altogether, the current study suggests that the supplemental intake of FO has a beneficial effect on osteogenesis.
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页数:19
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