Kim Jonggun, Park Yooheon, Park Yeonhwa
Department of Food Science, University of Massachusetts, Amherst, 102 Holdsworth Way, Amherst, MA 01003.
J Funct Foods. 2014 May 1;8:367-376. doi: 10.1016/j.jff.2014.04.006.
The inverse relationship between osteoblast and adipocyte differentiation in bone marrow mesenchymal stem cells has been linked to overall bone mass. It has previously been reported that conjugated linoleic acid (CLA) inhibits adipogenesis via a peroxisome-proliferator activated receptor-γ (PPARγ) mediated mechanism, while it increases osteoblastogenesis via a PPARγ-independent mechanism in mesenchymal stem cells. This suggests potential implication of CLA on improving bone mass. Thus the purpose of this study was to determine involvement of CLA on regulation of osteoblastogenesis in murine mesenchymal stem cells by focusing on the Mothers against decapentaplegic (MAD)-related family of molecules 8 (SMAD8), one of key regulators of osteoblastogenesis. The -10,-12 CLA, but not the -9,-11, significantly increased osteoblastogenesis via SMAD8, and inhibited adipogenesis independent of SMAD8, while inhibiting factors regulating osteoclastogenesis in this model. These suggest that CLA may help improve osteoblastogenesis via a SMAD8 mediated mechanism.
骨髓间充质干细胞中,成骨细胞与脂肪细胞分化之间的负相关关系与整体骨量有关。此前有报道称,共轭亚油酸(CLA)通过过氧化物酶体增殖物激活受体γ(PPARγ)介导的机制抑制脂肪生成,而在间充质干细胞中,它通过一种不依赖PPARγ的机制增加成骨细胞生成。这表明CLA在改善骨量方面具有潜在作用。因此,本研究的目的是通过聚焦成骨细胞生成的关键调节因子之一——与果蝇“抗五体不全”(MAD)相关分子家族8(SMAD8),来确定CLA在调节小鼠间充质干细胞成骨细胞生成中的作用。-10,-12 CLA而非-9,-11 CLA,通过SMAD8显著增加成骨细胞生成,并独立于SMAD8抑制脂肪生成,同时在该模型中抑制调节破骨细胞生成的因子。这些结果表明,CLA可能通过SMAD8介导的机制帮助改善成骨细胞生成。