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去卵巢大鼠骨质流失过程中骨髓间充质干细胞WNT/β-连环蛋白信号通路的变化及分化潜能

CHANGES OF WNT/B-CATENIN SIGNALING AND DIFFERENTIATION POTENTIAL OF BONE MARROW MESENCHYMAL STEM CELLS IN PROCESS OF BONE LOSS IN OVARIECTOMIZED RATS.

作者信息

Ren W, Gan D, Tan G, Xue H, Li N, Xu Z

机构信息

Weifang, China.

Jinan, China.

出版信息

Acta Endocrinol (Buchar). 2020 Apr-Jun;16(2):156-164. doi: 10.4183/aeb.2020.156.

Abstract

BACKGROUND

studies of the changes about osteoblastogenesis and adipogenesis potential of BMSCs were not clear. As it is the critical pathway for osteogenic differentiation and bone formation, whether or not Wnt/β-catenin signalling is involved in the changes of osteogenic and adipogenic potential of BMSCs and participates in bone content decrease of ovariectomized (OVX)osteoporosis rats has been rarely reported.

MATERIAL/METHODS: BMSCs from femurs of ovariectomzed rats were isolated and cultured . The proliferation potential of BMSCs was analysed by CCK-8 assays . Osteoblastic and adipogenic differentiation potential of the BMSCs was assessed by ALP activity assay, Alizarin red S staining, Oil red O staining and RT-PCR analysis.

RESULTS

The results demonstrated that BMSCs from bilateral ovariectomization rats were endowed with lower proliferation and osteoblastic differentiation potential but higher adipogenic potential than the control group . In addition, β-catenin was found to have been decreased in OVX BMSCs, indicating that Wnt/β-catenin signalling pathways were suppressed in OVX BMSCs .

CONCLUSIONS

Results suggested that changes in the Wnt canonical signalling pathway may be related to imbalances of osteogenic and adipogenic potential of BMSCs, and this may be an important factor related to bone content decrease in ovariectomized osteoporosis rats.

摘要

背景

关于骨髓间充质干细胞(BMSCs)成骨和成脂潜能变化的研究尚不明确。由于Wnt/β-连环蛋白信号通路是成骨分化和骨形成的关键途径,其是否参与BMSCs成骨和成脂潜能的变化以及是否参与去卵巢(OVX)骨质疏松大鼠骨量减少的过程,目前鲜有报道。

材料/方法:分离并培养去卵巢大鼠股骨中的BMSCs。通过CCK-8法分析BMSCs的增殖潜能。通过碱性磷酸酶(ALP)活性检测、茜素红S染色、油红O染色及逆转录-聚合酶链反应(RT-PCR)分析评估BMSCs的成骨和成脂分化潜能。

结果

结果表明,双侧去卵巢大鼠的BMSCs与对照组相比,增殖和成骨分化潜能较低,但成脂潜能较高。此外,发现OVX BMSCs中β-连环蛋白减少,表明OVX BMSCs中Wnt/β-连环蛋白信号通路受到抑制。

结论

结果提示,Wnt经典信号通路的变化可能与BMSCs成骨和成脂潜能失衡有关,这可能是去卵巢骨质疏松大鼠骨量减少的一个重要因素。

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