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Bushen Zhuangjin Decoction promotes chondrocyte proliferation by stimulating cell cycle progression

机译:补肾壮金汤通过刺激细胞周期进程促进软骨细胞增殖

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Bushen Zhuangjin Decoction (BZD), a well-known formulation in Traditional Chinese Medicine, has been widely used for the treatment of osteoarthritis (OA). Due to the poor intrinsic repair capacity of chondrocytes, promoting the proliferation of chondrocytes is an efficient treatment to delay the progression of cartilage degradation. The present study, therefore, focused on the effect of BZD on chondrocyte proliferation, exploring the mechanism of BZD on the inhibition of cartilage degradation. Chondrocytes isolated from the knee articular cartilage of Sprague Dawley rats were cultured and identified by type II collagen immunohistochemistry. It was found that BZD promoted chondrocyte viability in a dose- and time-dependent manner. To investigate if BZD promoted the chondrocyte viability by stimulating the cell cycle progression a flow cytometer was used, and the results showed that the percentage proportion of G0/G1 cells was significantly lower, and the percentage proportion of S cells was significantly higher, in treated cells compared with that in untreated cells. To gain insight into the mechanism underlying the effect of BZD on the cell cycle progression, the mRNA and protein expression of cyclin D1, cyclin-dependent kinase 4 (CDK4), CDK6 and p21 was measured by reverse transcription-polymerase chain reaction and western blotting, respectively. The mRNA and protein expression of cyclin D1, CDK4 and CDK6 in the BZD-treated chondrocytes was significantly upregulated, while the mRNA and protein expression of p21 was significantly downregulated, compared with that in the untreated chondrocytes. These results suggested that BZD promoted chondrocyte proliferation by accelerating G1/S transition, indicating that BZD is a potential therapeutic agent for the treatment of OA.
机译:补肾壮津汤(BZD)是中药中的著名配方,已被广泛用于治疗骨关节炎(OA)。由于软骨细胞固有的修复能力差,促进软骨细胞的增殖是延迟软骨降解进程的有效方法。因此,本研究集中于BZD对软骨细胞增殖的影响,探讨BZD抑制软骨降解的机制。培养从Sprague Dawley大鼠的膝关节软骨分离的软骨细胞,并通过II型胶原免疫组织化学鉴定。发现BZD以剂量和时间依赖性方式促进软骨细胞的活力。为了研究BZD是否通过刺激细胞周期进程来促进软骨细胞的活力,使用了流式细胞仪,结果显示,在治疗中,G0 / G1细胞的百分比显着降低,而S细胞的百分比显着更高。与未处理的细胞相比。为了深入了解BZD影响细胞周期进程的机制,通过逆转录-聚合酶链反应和Western印迹检测了cyclin D1,cyclin依赖性激酶4(CDK4),CDK6和p21的mRNA和蛋白表达。 , 分别。与未处理的软骨细胞相比,BZD处理的软骨细胞中cyclin D1,CDK4和CDK6的mRNA和蛋白表达显着上调,而p21的mRNA和蛋白表达则显着下调。这些结果表明BZD通过加速G1 / S过渡来促进软骨细胞增殖,表明BZD是治疗OA的潜在治疗剂。

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