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Up-regulation of connexin 43 and gap junctional intercellular communication by Coleusin Factor is associated with growth inhibition in rat osteosarcoma UMR106 cells

机译:胶原蛋白上调连接蛋白43和间隙连接细胞间通讯与大鼠骨肉瘤UMR106细胞的生长抑制有关

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摘要

Gap junctions, formed by connexin (Cx) family proteins, permit direct exchange of regulatory ions and small signal molecules between neighbouring cells. Gap junctional intercellular communication (GJIC) plays an important role in maintaining the homeostasis and preventing cell transformation. Most of the tumour cells feature deficient or aberrant connexin expression and GJIC level, and restoration of connexin expression and GJIC is correlated with cell growth control. Numerous researches has suggested the possibility of connexins as potential anti-tumour targets for chemoprevention and chemotherapy. We investigated the ability of Coleusin Factor (CF, also named FSK88) to regulate the Cx43 expression and GJIC level in rat osteosarcoma UMR106 cells. The results have demonstrated that CF increased the mRNA and protein expression of Cx43 in both in a dose- and timedependent manner, and concomitant with up-regulation of Cx43, CF treatment up-regulated the diminished GJIC level in UMR106 cells as assayed by dye transfer experiments. In addition, Cx43 distribution at the plasma membrane was also enhanced dramatically by CF treatment. Furthermore, we discovered that CF was potent to inhibit the growth and proliferation of UMR106 cells. These results provide the first evidence that CF can regulate connexin and GJIC, indicating that Cx43 may be a target of CF to exert its anti-tumour effects.
机译:连接蛋白(Cx)家族蛋白形成的间隙连接点允许相邻细胞之间直接交换调节离子和小信号分子。间隙连接细胞间通讯(GJIC)在维持体内平衡和防止细胞转化中起重要作用。大多数肿瘤细胞具有连接蛋白表达和GJIC水平不足或异常,并且连接蛋白表达和GJIC的恢复与细胞生长控制相关。大量研究表明,连接蛋白有可能成为化学预防和化学疗法的潜在抗肿瘤靶标。我们研究了胭脂蛋白因子(CF,也称为FSK88)调节大鼠骨肉瘤UMR106细胞中Cx43表达和GJIC水平的能力。结果表明,CF以剂量和时间依赖性方式增加Cx43的mRNA和蛋白表达,并且随着Cx43的上调,CF处理上调了UMR106细胞中GJIC水平的降低(通过染料转移分析)实验。此外,CF处理还大大提高了质膜上Cx43的分布。此外,我们发现CF有效抑制UMR106细胞的生长和增殖。这些结果提供了CF可以调节连接蛋白和GJIC的第一个证据,表明Cx43可能是CF发挥其抗肿瘤作用的靶标。

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