Department of Biologic and Materials Sciences and Division of Prosthodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
Department of Orthodontics, Jilin University School and Hospital of Stomatology, Changchun, Jilin, China.
J Bone Miner Res. 2018 Nov;33(11):2021-2034. doi: 10.1002/jbmr.3530. Epub 2018 Jul 19.
A reduction in trabecular bone mass is often associated with an increase in marrow fat in osteoporotic bones. The molecular mechanisms underlying this inverse correlation are incompletely understood. Here, we report that mice lacking tuberous sclerosis 1 (Tsc1) in Osterix-expressing cells had a significant decrease in trabecular bone mass characterized by decreased osteoblastogenesis, increased osteoclastogenesis, and increased bone marrow adiposity in vivo. In vitro study showed that Tsc1-deficient bone marrow stromal cells (BMSCs) had decreased proliferation, decreased osteogenic differentiation, and increased adipogenic differentiation in association with the downregulation of Wnt/β-catenin signaling. Mechanistically, TSC1 deficiency led to autophagy suppression and consequent Notch1 protein increase, which mediated the GSK3β-independent β-catenin degradation. Together, our results indicate that Tsc1 controls the balance between osteoblast and adipocyte differentiation of BMSCs. © 2018 American Society for Bone and Mineral Research.
松质骨量减少通常与骨质疏松骨骨髓脂肪增加有关。这种负相关的分子机制尚不完全清楚。在这里,我们报告说,在成骨细胞特异性表达 Osterix 的细胞中缺乏结节性硬化症 1 (Tsc1) 的小鼠,体内表现出明显的小梁骨量减少,其特征为成骨细胞生成减少、破骨细胞生成增加和骨髓脂肪增多。体外研究表明,Tsc1 缺陷型骨髓基质细胞 (BMSCs) 的增殖减少,成骨分化减少,脂肪生成分化增加,与 Wnt/β-catenin 信号转导下调有关。在机制上,TSC1 缺陷导致自噬抑制和随后 Notch1 蛋白增加,从而介导 GSK3β 非依赖性 β-catenin 降解。总之,我们的研究结果表明,Tsc1 控制着 BMSCs 中成骨细胞和脂肪细胞分化之间的平衡。