首页> 美国卫生研究院文献>Journal of Cellular and Molecular Medicine >Protective effect of Agrimonia pilosa polysaccharides on dexamethasone‐treated MC3T3‐E1 cells via Wnt/β‐Catenin pathway
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Protective effect of Agrimonia pilosa polysaccharides on dexamethasone‐treated MC3T3‐E1 cells via Wnt/β‐Catenin pathway

机译:仙鹤草多糖通过Wnt /β-Catenin途径对地塞米松处理的MC3T3-E1细胞的保护作用

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摘要

A water‐soluble polysaccharide (APP‐AW) was isolated from and prepared to three sulphated derivatives (S1, S2 and S3). The results showed that pre‐treatment with APP‐AW, S1, S2 and S3 each at the concentration of 50 μg/mL for 48 hours was able to prevent cytotoxicity induced by 1 μmol/L dexamethasone (Dex) in MC3T3‐E1 cells via inhibition of apoptosis, which is in line with the findings in flow cytometry analysis. Meanwhile, the decreased ALP activity, collagen content, mineralization, BMP2, Runx2, OSX and OCN protein expression in DEX‐treated MC3T3‐E1 cells were reversed by the addition of APP‐AW, S1, S2 and S3. Moreover, APP‐AW, S1, S2 and S3 rescued DEX‐induced increase of Bax, cytochrome c and caspase‐3 and decrease of Bcl‐2, Wnt3, β‐catenin and c‐Myc protein expression in MC3T3‐E1 cells. Our findings suggest that pre‐treatment with APP‐AW, S1, S2 and S3 could significantly protect MC3T3‐E1 cells against Dex‐induced cell injury via inhibiting apoptosis and activating Wnt/β‐Catenin signalling pathway, thus application of these polysaccharides may be a promising alternative strategy for steroid‐induced avascular necrosis of the femoral head (SANFH) therapy.
机译:从三种硫酸化衍生物(S1,S2和S3)中分离出水溶性多糖(APP-AW)并制备成水溶性的多糖。结果表明,分别以50μg/ mL的浓度对APP‐AW,S1,S2和S3进行48小时的预处理可以通过1μmol/ L地塞米松(Dex)通过MC3T3-E1细胞预防细胞毒性抑制细胞凋亡,这与流式细胞仪分析的结果一致。同时,通过添加APP‐AW,S1,S2和S3可以逆转DEX处理的MC3T3-E1细胞中ALP活性,胶原蛋白含量,矿化,BMP2,Runx2,OSX和OCN蛋白表达的下降。此外,APP‐AW,S1,S2和S3挽救了DEX诱导的MC3T3-E1细胞中Bax,细胞色素c和caspase-3的增加以及Bcl-2,Wnt3,β-catenin和c-Myc蛋白表达的减少。我们的发现表明,用APP‐AW,S1,S2和S3进行预处理可以通过抑制细胞凋亡和激活Wnt /β-Catenin信号通路来显着保护MC3T3-E1细胞免受Dex诱导的细胞损伤,因此这些多糖的应用可能是激素引起的股骨头缺血性坏死(SANFH)治疗的一种有希望的替代策略。

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