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Role of transforming growth factor-β pathway in the mechanism of wound healing by saponin from Ginseng Radix rubra

机译:人参总皂甙中转化生长因子-β途径在伤口愈合机制中的作用

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摘要

The effects of saponin from Ginseng Radix rubra on extracellular matrix metabolism, the activation and synthesis of TGF-β1, and the modification of TGF-β receptor in fibroblasts were examined to elucidate the contribution of the TGF-β pathway to the mechanism of wound healing by saponin.Fibronectin synthesis was analysed by the immunoprecipitation method. Activation and synthesis of TGF-β1 were measured by ELISA. The expressions of TGF-β receptors in fibroblasts were examined at protein and mRNA levels by the cross-linking method and Northern blot analysis, respectively.The fibronectin synthesis increased 2.3- and 3.9-fold at fibroblasts treated with 1 and 10 μg ml−1 of saponin, respectively, compared with that in non-treated cells. Fibronectin synthesis stimulated with 10 μg ml−1 of saponin was inhibited with 69% by 5 μg ml−1 of an anti-TGF-β1 antibody. mRNA of TGF-β type I receptor increased 4.8- and 4.4-fold at fibroblasts treated with 1 and 10 μg ml−1 of saponin, respectively, and that of TGF-β type II receptor also increased 3.4- and 3.2-fold at fibroblasts treated with 1 and 10 μg ml−1 of saponin, respectively. The significant increases of TGF-β type I and II receptors and of fibronectin synthesis were observed at the same concentrations of saponin. TGF-β1 content increased 1.74- and 1.87-fold at conditioned medium of fibroblasts treated with 100 and 250 μg ml−1 of saponin, respectively, higher concentrations than those which accelerated fibronectin synthesis. Furthermore, the active TGF-β1 content was below 10% of total TGF-β1 at each concentration of saponin.These results indicate that saponin stimulates fibronectin synthesis through the changes of TGF-β receptor expressions in fibroblasts.
机译:研究了人参总皂苷对成纤维细胞胞外基质代谢,TGF-β1活化和合成以及TGF-β受体修饰的影响,以阐明TGF-β途径对伤口愈合机制的贡献用免疫沉淀法分析纤连蛋白的合成。通过ELISA测量TGF-β1的活化和合成。用交联法和RNA印迹法分别检测了成纤维细胞中TGF-β受体的表达水平。用1和10μg/ ml-1处理的成纤维细胞中,纤连蛋白的合成增加了2.3-和3.9-倍。与未经处理的细胞相比,皂苷的含量分别更高。用5μgμml-1的抗TGF-β1抗体可抑制由10μgμml-1的皂苷刺激的纤连蛋白合成,抑制率为69%。 TGF-βI型受体的mRNA在用1和10μg/ ml-1皂苷处理的成纤维细胞中分别增加了4.8和4.4倍,而TGF-βII型受体的mRNA在成纤维细胞中分别增加了3.4和3.2倍。分别用1和10μg/ ml-1的皂苷处理。在相同的皂苷浓度下,观察到TGF-βI型和II型受体和纤连蛋白合成显着增加。在分别用100和250μg/ ml-1皂苷处理的成纤维细胞的条件培养基中,TGF-β1的含量分别增加了1.74倍和1.87倍,其浓度高于促进纤连蛋白合成的浓度。此外,在每个皂苷浓度下,活性TGF-β1的含量都低于总TGF-β1的10%。这些结果表明,皂苷通过成纤维细胞中TGF-β受体表达的变化刺激了纤连蛋白的合成。

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