节点文献

外源性三碘甲腺原氨酸对鸭胚肝细胞活性及Ⅲ型脱碘酶基因表达的影响

Effect of T3 on Activity and Expression of D3 mRNA of Liver Cells in Duck Embryo

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 孙文强胡艳李慧芳陈宽维

【Author】 SUN Wenqiang;HU Yan;LI Huifang;CHEN Kuanwei;Poultry Institute,Chinese Academy of Agricultural Science;

【机构】 中国农业科学院家禽研究所

【摘要】 研究以鸭15日胚龄肝脏细胞为试验素材,以终浓度为5 ng/m L的三碘甲腺原氨酸(T3)稀释液及等体积的生理盐水对肝细胞干扰36 h,依次将两组细胞设定为试验组和对照组。采用Cell counting kit-8(CCK-8)法和实时荧光定量PCR方法分别检测干扰后培养0、12、24 h时细胞活性及Ⅲ型脱碘酶(D3)mRNA表达。结果表明,在三个检测时间点,试验组肝细胞活性均显著高于对照组(P=0.026,P=0.006,P=0.013),且在干扰后培养24 h时两组细胞活性在组内均显著高于0和12 h(P=0.000,P=0.000);0和12 h时两组细胞中D3 mRNA表达量在组间和组内均没有发生显著变化,24 h时对照组肝细胞中D3 mRNA表达量显著下调且显著低于试验组(P=0.000,P=0.000)。结论:外源性T3能够促进鸭15日胚龄肝脏细胞的生长,D3在肝细胞增殖过程中可能发挥正向调控的作用。

【Abstract】 In this study,liver cells of duck at 15 th embryo days were cultured,and the same volume of T3(final concentration 5 ng/m L)and physiological saline were added into the cells cultured for 36 h,defined as interference and control groups,respectively. The cell activity and D3 mRNA expression in cells were evaluated by CCK-8 and Real-time fluorescent quantitative PCR(RT-QPCR)at 0,12 and 24 h after T3 interference,respectively. The results showed that the activity of the treatment cells were significant higher than that of control groups at three times(P=0.026,0.006,0.013),and the activity at 24 h in two groups were all higher than that at 0 and 12 h(P=0.000,P=0.000,). There was no significant difference for all possible combinations of groups at 0 and 12 h. The expression of D3 mRNA in control group at 24 h descended and was significant lower than that of control groups at 0 and 12 h(P<0.01)and the interference group at 24 h(P=0.000). These results indicated that the exogenous T3 could promote the growth of duck embryo liver cells,and D3 might play a positive role in the proliferation of liver cells.

【关键词】 T3肝细胞细胞活性D3基因表达
【Key words】 duckT3liver cellsactivity of cellexpression of D3 mRNA
【基金】 国家自然科学基金(31172194);江苏省科技支撑计划项目(BE2012460;BE2014362)
  • 【分类号】S834.5
  • 【下载频次】58
节点文献中: 

本文链接的文献网络图示:

本文的引文网络