WANG Yujie, AN Fangyu, YAN Chunlu, SONG Jiayi, CHANG Weirong, ZHANG Jie, XIAO Zhipan, GAO Peng, LI Zhonghong. Research Progress of Potential Regulatory Effects on Osteoporosis by BMP-mediated Smad Dependent and Smad Independent Pathways[J]. Chinese Journal of Modern Applied Pharmacy, 2024, 41(2): 277-286. DOI: 10.13748/j.cnki.issn1007-7693.20231899
    Citation: WANG Yujie, AN Fangyu, YAN Chunlu, SONG Jiayi, CHANG Weirong, ZHANG Jie, XIAO Zhipan, GAO Peng, LI Zhonghong. Research Progress of Potential Regulatory Effects on Osteoporosis by BMP-mediated Smad Dependent and Smad Independent Pathways[J]. Chinese Journal of Modern Applied Pharmacy, 2024, 41(2): 277-286. DOI: 10.13748/j.cnki.issn1007-7693.20231899

    Research Progress of Potential Regulatory Effects on Osteoporosis by BMP-mediated Smad Dependent and Smad Independent Pathways

    • Osteoporosis can be induced by various factors including prolonged glucocorticoid usage, diminished estrogen levels, secondary hyperparathyroidism, and alterations in the microenvironment of bone tissue. The bone metabolism imbalance(osteogenic-lipogenic imbalance) plays a crucial role in the development of osteoporosis. This imbalance is primarily driven by an increase in the differentiation of bone marrow mesenchymal stem cells into adipocytes and a decrease in their differentiation into osteoblasts, thus forming the core of the osteogenic-lipogenic imbalance observed in osteoporosis. The bone morphogenesis protein(BMP) plays a crucial role in the regulation of the osteogenic-lipid balance in osteoporosis. This regulatory function is accomplished through both the Smad-dependent and Smad-independent pathways. This review centers on the Smad-dependent and Smad-independent pathways facilitated by BMP, offering a comprehensive overview of the potential mechanisms through which BMP-2, 4, 6, 7, and 9 contribute to the regulation of osteogenesis and lipid metabolism in osteoporosis via these pathways. In order to present novel insights for the identification of efficacious targets for clinical anti-osteoporosis medications.
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