首页> 外文期刊>Chinese Journal of Clinical Oncology >Inhibition of Differentiation by Transforming Growth Factor β1 in Rhabdomyosarcoma Cells
【24h】

Inhibition of Differentiation by Transforming Growth Factor β1 in Rhabdomyosarcoma Cells

机译:转化生长因子β1对横纹肌肉瘤细胞分化的抑制作用

获取原文
           

摘要

OBJECTIVE To study the effect of transforming growth factor β1 (TGF-β1) on differentiation of rhabdomyosarcoma (RMS) cells METHODS RD (human embryonal RMS cell line) cells, cultured in differentiation medium containing 9-cis retinoic acid (9CRA), were treated with TGF-β1. Proliferation of the cells was examined by the MTT assay. The differentiation specific proteins (sarcomeric actin and MyHC) and myogenic transcription factors (MyoD1 and myogenin) in the RD cells were assessed by immunofluorescence staining. rnRESULTS Compared to control cells, treatment with lower concentrations of TGF-β1 (0.1 and 0.2 ng/ml) induced an increase in OD values after 4 d (P< 0.01), whereas higher concentrations of TGF-β1 (2 and 5 ng/ml) led to a reduction of cell viability (P< 0.01). After exposure to 9CRA, the viability of the cells decreased significantly (P< 0.01), while sarcomeric actin, MyHC and myogenin were induced. These changes were antagonized by TGF-β1 (0.1 ng/ml). No changes were observed in expression of MyoD1. CONCLUSION The RMS cells, derived from myogenic progenitors are committed to a myogenic fate, but are arrested in the differentiation course by the addition of TGF-β1 which represses some of the myogenic transcription factors.
机译:目的研究转化生长因子β1(TGF-β1)对横纹肌肉瘤(RMS)细胞分化的影响。方法研究在含9-顺式视黄酸(9CRA)的分化培养基中培养的RD(人胚RMS细胞系)细胞用TGF-β1。通过MTT测定法检查细胞的增殖。通过免疫荧光染色评估RD细胞中的分化特异性蛋白(肌节肌动蛋白和MyHC)和肌转录因子(MyoD1和肌生成素)。结果与对照细胞相比,用较低浓度的TGF-β1(0.1和0.2 ng / ml)处理后4 d OD值增加(P <0.01),而较高浓度的TGF-β1(2和5 ng / ml)处理ml)导致细胞活力降低(P <0.01)。暴露于9CRA后,细胞活力显着下降(P <0.01),同时诱导了肌节肌动蛋白,MyHC和肌生成素。这些变化被TGF-β1(0.1 ng / ml)拮抗。没有观察到MyoD1表达的变化。结论起源于成肌祖细胞的RMS细胞具有成肌命运,但通过加入TGF-β1抑制了某些成肌转录因子而在分化过程中被阻滞。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号