High water-soluble curcuminoids-rich extract regulates osteogenic differentiation of MC3T3-E1 cells: Involvement of Wnt/β-catenin and BMP signaling pathway

被引:9
|
作者
Pengjam, Yutthana [1 ]
Syazwani, Nurul [2 ]
Inchai, Jakkapong [1 ]
Numit, Amornkan [1 ]
Yodthong, Thanintorn [3 ]
Pitakpornpreecha, Thanawat [3 ]
Panichayupakaranant, Pharkphoom [2 ]
机构
[1] Prince Songkla Univ, Fac Med Technol, Hat Yai 90110, Thailand
[2] Prince Songkla Univ, Fac Pharmaceut Sci, Hat Yai 90112, Thailand
[3] Prince Songkla Univ, Fac Sci, Hat Yai 90110, Thailand
关键词
BMP signaling; curcuminoid; osteoporosis; solid dispersion; water soluble; Wnt/beta-catenin; OSTEOBLAST DIFFERENTIATION; CHEMOPREVENTIVE AGENT; BONE LOSS; MECHANISMS; WNT; ACTIVATION; PIPERINE;
D O I
10.1016/j.chmed.2021.01.003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Objective: The present study aimed to evaluate the effect of a high water-soluble curcuminoids-rich extract (CRE) in a solid dispersion form (CRE-SD) using polyvinylpyrrolidone K30 on osteogenic induction of MC3T3-E1 cells. Methods: CRE was pre-purified using a microwave assisted extraction couple with a Diaion (R) HP-20 column chromatography. The osteoblastic cell proliferation and differentiation potentials of CRE-SD in MC3T3-E1 cells were tested by cell viability, alkaline phosphatase (ALP) activity, and Alizarin red S activity assays. The mRNA expressions of osteoblast-specific genes and underline mechanisms were assessed by a real time PCR and western blot analysis. Results: CRE-SD 50 mu g/mL increased alkaline phosphatase (ALP) activity, an early differentiation marker of osteoblasts in both MC3T3-E1 cells and non-osteogenic mouse pluripotent cell line, C3H10T1/2, indicating the action of CRE-SD was not cell-type specific. Alizarin red S activity showed a significant amount of calcium deposition in cells treated with CRE-SD. CRE-SD also upregulated the mRNA expression levels of transcription factors that favor osteoblast differentiation including Bmp-2, Runx2 and Collagen 1a, in a dose dependent manner. Western blot analysis revealed that noggin attenuated CRE-SD-promoted expressions of Bmp-2 and Runx2 proteins. siRNA mediated blocking of Wnt/beta-catenin signaling pathway also annulled the influence of CRE-SD, indicating Wnt/beta-catenin dependent activity. Inhibition of the different signaling pathways abolished the influence of CRE-SD on ALP activity, confirming that CRE-SD induced MC3T3-E1 cells into osteoblasts through Wnt/beta-catenin and BMP signaling pathway. Conclusion: These results collectively demonstrate that CRE-SD may be a potential therapeutic agent for the treatment of osteoporosis. (C) 2021 Tianjin Press of Chinese Herbal Medicines. Published by ELSEVIER B.V.
引用
收藏
页码:534 / 540
页数:7
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