首页> 外文会议>The 6th International Conference on Biomedical Engineering and Rehabilitation Engineering (ICBME '2002) May 27-30, 2002 Guilin, China >THE HARD SEGMENT OF POLYURETHANE WITH THE TUMOR-PROMOTING ACTIVITY MEDIATED BY CONNEXIN 43 AND ITS PHOSPHORYLATION ON V79 CELL LINE
【24h】

THE HARD SEGMENT OF POLYURETHANE WITH THE TUMOR-PROMOTING ACTIVITY MEDIATED BY CONNEXIN 43 AND ITS PHOSPHORYLATION ON V79 CELL LINE

机译:Connexin 43介导的具有促肿瘤活性的聚氨酯硬段及其在V79细胞株上的磷酸化

获取原文
获取原文并翻译 | 示例

摘要

In this investigation we studied the roles of the connexin 43 and its phosphorylation form, a major intercellular communication protein, in the tumorigenesis induced by hard segment of polyurethane. The hard segment, 4,4'-di (ethoxycarboamide) diphenymethane (MDU), significantly reduce the quality of connexin 43 and mainly increase the connexin 43 phosphorylation on serine, slightly increase the phosphorylation on tyrosine and threonine. PU4 and PU8 decrease the amount of connexin 43 and increase the connexin 43 phosphorylation on serine and theonine. The gap junctional permeability measured with Lucifer Yellow also shown that the MDU reduce the cell-cell communication. The results indicated that the hard segment of polyurethane have the tumor-promoting activity and mediated by the connexin 43 and its phosphorylation.
机译:在这项研究中,我们研究了连接蛋白43及其磷酸化形式(一种主要的细胞间通讯蛋白)在聚氨酯硬链段诱导的肿瘤发生中的作用。硬链段4,4'-二(乙氧基甲酰胺)联苯甲烷(MDU)显着降低了连接蛋白43的质量,主要增加了丝氨酸上连接蛋白43的磷酸化,略微增加了酪氨酸和苏氨酸上的磷酸化。 PU4和PU8减少连接蛋白43的量,并增加连接蛋白43在丝氨酸和茶氨酸上的磷酸化。用路西法·黄测量的间隙连接渗透性还表明,MDU减少了细胞间的通讯。结果表明,聚氨酯的硬段具有促肿瘤活性,并由连接蛋白43及其磷酸化介导。

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