Preptin promotes proliferation and osteogenesis of MC3T3-E1 cells by upregulating β-catenin expression

被引:15
|
作者
Xiao, Chunyuan [1 ]
Li, Wei [1 ]
Lu, Tianlin [1 ]
Wang, Jiayi [1 ]
Han, Jie [1 ]
机构
[1] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Rheumatol, Shanghai 200120, Peoples R China
关键词
preptin; Wnt; beta-catenin signalling pathway; osteoporosis; osteogenesis; WNT SIGNALING PATHWAY; GROWTH-FACTOR-II; BONE-FORMATION; IN-VITRO; DIFFERENTIATION; INSULIN; RUNX2; OSTEOPOROSIS; PLAYERS; MASS;
D O I
10.1002/iub.2016
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
Preptin, an oligopeptide secreted by pancreatic beta-cell, plays a significant role in glycometabolism and bone metabolism. Preptin strengthens proliferation and differentiation of osteoblasts, but the mechanism is unclear. Here, we explored the role of the Wnt/beta-catenin signaling pathway which is well known to affect bone development and remodelling in the function of preptin. We found that preptin promoted the cell proliferative activity and osteoblastic differentiation in osteoblast-like MC3T3-E1 cells in a dose-independent manner, as evidenced by elevation in osteogenic genes, alkaline phosphatase activity and alizarin red staining in a dose-independent manner. Additionally, our findings demonstrated that the beta-catenin expression level and runt-related transcription factor 2, which is the key downstream target of this pathway, were increased. The Wnt/beta-catenin signalling pathway antagonist DKK1 abrogated the proliferative effect and differentiation function of preptin in MC3T3-E1 cells. These data indicated that preptin may be a potential therapeutic target for the treatment of osteoporosis and that osteogenic impact of preptin in MC3T3-E1 cells might be mediated by the Wnt/beta-catenin signalling pathway. (c) 2019 IUBMB Life, 9999(9999):1-9, 2019
引用
收藏
页码:854 / 862
页数:9
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