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Cinobufotalin prevents bone loss induced by ovariectomy in mice through the BMPs/SMAD and Wnt/β-catenin signaling pathways
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作者 Da-zhuang Lu Li-jun Zeng +8 位作者 Yang Li Ran-li Gu Meng-long Hu Ping Zhang Peng Yu Xiao Zhang Zheng-wei Xie Hao Liu Yong-sheng Zhou 《Animal Models and Experimental Medicine》 CAS CSCD 2024年第3期208-221,共14页
Background:Osteoporosis is a chronic bone disease characterized by bone loss and decreased bone strength.However,current anti-resorptive drugs carry a risk of various complications.The deep learning-based efficacy pre... Background:Osteoporosis is a chronic bone disease characterized by bone loss and decreased bone strength.However,current anti-resorptive drugs carry a risk of various complications.The deep learning-based efficacy prediction system(DLEPS)is a forecasting tool that can effectively compete in drug screening and prediction based on gene expression changes.This study aimed to explore the protective effect and potential mechanisms of cinobufotalin(CB),a traditional Chinese medicine(TCM),on bone loss.Methods:DLEPS was employed for screening anti-osteoporotic agents according to gene profile changes in primary osteoporosis.Micro-CT,histological and morphological analysis were applied for the bone protective detection of CB,and the osteogenic differentiation/function in human bone marrow mesenchymal stem cells(hBMMSCs)were also investigated.The underlying mechanism was verified using qRT-PCR,Western blot(WB),immunofluorescence(IF),etc.Results:A safe concentration(0.25mg/kg in vivo,0.05μM in vitro)of CB could effectively preserve bone mass in estrogen deficiency-induced bone loss and promote osteogenic differentiation/function of hBMMSCs.Both BMPs/SMAD and Wnt/β-catenin signaling pathways participated in CB-induced osteogenic differentiation,further regulating the expression of osteogenesis-associated factors,and ultimately promoting osteogenesis.Conclusion:Our study demonstrated that CB could significantly reverse estrogen deficiency-induced bone loss,further promoting osteogenic differentiation/function of hBMMSCs,with BMPs/SMAD and Wnt/β-catenin signaling pathways involved. 展开更多
关键词 BMPs/SMAD bone loss cinobufotalin hbmmscs OSTEOGENESIS OSTEOPOROSIS Wnt/β-catenin signaling pathways
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人骨髓间质干细胞的培养及成骨功能研究 被引量:4
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作者 王衣祥 李盛林 +3 位作者 武登诚 章魁华 于世凤 崔胜先 《中华口腔医学杂志》 CAS CSCD 北大核心 2003年第6期467-469,C007,共4页
目的 体外扩增人骨髓间质干细胞 (humanbonemarrow derivedmesonchymalstemcells,hBMMSCs) ,研究其生物学特征及体内、外成骨功能。方法 分离培养hBMMSCs,并对其形态、增殖动力学、碱性磷酸酶 (alkalinephosphatase,ALP)表达及体内、... 目的 体外扩增人骨髓间质干细胞 (humanbonemarrow derivedmesonchymalstemcells,hBMMSCs) ,研究其生物学特征及体内、外成骨功能。方法 分离培养hBMMSCs,并对其形态、增殖动力学、碱性磷酸酶 (alkalinephosphatase,ALP)表达及体内、外成骨功能进行研究。结果 hBMMSCs可在体外培养扩增 ,群体倍增时间约为 3 5d。ALP检测表明 ,未经矿化诱导的hBMMSCs可表达少量ALP ,诱导后其表达量明显增高。vonkossa染色证实在矿化诱导液作用下hBMMSCs在体外可形成钙结节。体内成骨实验证实 ,1× 10 5个hBMMSCs接种到 30mm3 块状HA/TCP载体移植BALB/C裸小鼠皮下 3个月 ,可观察到层板状骨组织生成。结论 hBMMSCs是一种具有成骨潜能的前体细胞 ,经培养、扩增、诱导后 ,在体外可形成矿化结节 ,体内可在载体表面形成骨组织。 展开更多
关键词 骨髓间质干细胞 hbmmscs 成骨功能 碱性磷酸酶 细胞培养 口腔颌面部
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