首页> 外文期刊>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:Agrimonia pilosa多糖在Wnt /β-catenin途径通过Wnt /β-catenin途径对地塞米松处理MC3T3-E1细胞的保护作用

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摘要

A water‐soluble polysaccharide (APP‐AW) was isolated from Agrimonia pilosa 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Agrimonia pilosa中分离出水溶性多糖(APP-AW)并制备三种硫酸化衍生物(S1,S2和S3)。结果表明,用APP-AW,S1,S2和S3预处理,每个浓度为50Ωμg/ ml,48Ω小时能够防止在MC3T3-中诱导的1·μmol/ L地塞米松(DEX)诱导的细胞毒性通过抑制细胞凋亡的E1细胞,这与流式细胞术分析中的结果一致。同时,通过添加APP-AW,S1,S2和S3来反转在DEX处理的MC3T3-E1细胞中降低的ALP活性,胶原蛋白含量,矿化,BMP2,RUNX2,OSX和OCN蛋白表达。此外,APP-AW,S1,S2和S3拯救了Dex诱导的Bax,细胞色素C和Caspase-3的增加,并在MC3T3-E1细胞中降低了Bcl-2,Wnt3,β-catenin和C-myc蛋白表达。我们的研究结果表明,使用APP-AW,S1,S2和S3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,因此可以应用这些多糖对股骨头(SANFH)治疗的类固醇诱导的缺血性坏死的有前途的替代策略。

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