Zhang Lili, Liu Mengmeng, Zhou Xiaokang, Liu Yi, Jing Bo, Wang Xiaogang, Zhang Qi, Sun Yao
Department of Implantology, School and hospital of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, China.
Cell Physiol Biochem. 2016;40(3-4):681-692. doi: 10.1159/000452580. Epub 2016 Nov 30.
BACKGROUND/AIMS: Bone marrow adipogenesis is one of the major characteristics of aged bone. Bone marrow mesenchymal stem cells (BMMSCs) prefer to differentiate into adipocytes instead of osteoblasts in the bone marrow cavity in aged hosts. The mechanism of formation and function of adipocytes in aged bone marrow needs further investigation. Osteoprotegerin (OPG) is a member of the tumor necrosis factor receptor (TNFR) super family, and it can inhibit the activities of osteoclasts. We found that adipocyte numbers increased in the bone marrow of Opg knockout mice. In this study, we investigated the role of OPG in the differentiation of BMMSCs and bone marrow adipogenesis.
Histological analyses were performed on the bone tissues of Opg knockout (Opg-KO) and wild-type (WT) mice of different ages. BMMSCs obtained from mice were cultured in vitro to evaluate their differentiation abilities.
With aging, the expression of Opg in the bone marrow of WT mice markedly decreased, but that of the adipogenic specific transcription factor peroxisome proliferator-activated receptor γ (Ppar-γ) increased. Adipocytes formed in the bone marrow of Opg-KO mice at a relative young age, and the number of adipocytes increased dramatically with age. Compared with the WT control, the osteogenic differentiation of Opg-KO BMMSCs decreased, but the adipogenic differentiation increased. Moreover, exogenous OPG could inhibit the adipogenic differentiation and promote the osteogenic differentiation of Opg-KO BMMSCs in vitro.
OPG plays an important role in regulating BMMSC differentiation and bone marrow adipogenesis.
背景/目的:骨髓脂肪生成是衰老骨骼的主要特征之一。在老年宿主体内,骨髓间充质干细胞(BMMSCs)更倾向于在骨髓腔内分化为脂肪细胞而非成骨细胞。老年骨髓中脂肪细胞的形成机制和功能有待进一步研究。骨保护素(OPG)是肿瘤坏死因子受体(TNFR)超家族的成员,它可以抑制破骨细胞的活性。我们发现Opg基因敲除小鼠骨髓中的脂肪细胞数量增加。在本研究中,我们探讨了OPG在BMMSCs分化和骨髓脂肪生成中的作用。
对不同年龄的Opg基因敲除(Opg-KO)小鼠和野生型(WT)小鼠的骨组织进行组织学分析。对从小鼠获取的BMMSCs进行体外培养以评估其分化能力。
随着年龄增长,WT小鼠骨髓中Opg的表达显著降低,但脂肪生成特异性转录因子过氧化物酶体增殖物激活受体γ(Ppar-γ)的表达增加。Opg-KO小鼠在相对年轻时骨髓中就形成了脂肪细胞,且脂肪细胞数量随年龄急剧增加。与WT对照组相比,Opg-KO BMMSCs的成骨分化降低,但脂肪生成分化增加。此外,外源性OPG可在体外抑制Opg-KO BMMSCs的脂肪生成分化并促进其成骨分化。
OPG在调节BMMSC分化和骨髓脂肪生成中起重要作用。