首页> 外文期刊>Cell death and differentiation >Mtd/Bok takes a swing: proapoptotic Mtd/Bok regulates trophoblast cell proliferation during human placental development and in preeclampsia.
【24h】

Mtd/Bok takes a swing: proapoptotic Mtd/Bok regulates trophoblast cell proliferation during human placental development and in preeclampsia.

机译:Mtd / Bok摇摆不定:凋亡的Mtd / Bok在人胎盘发育和子痫前期调节滋养细胞增殖。

获取原文
获取原文并翻译 | 示例
           

摘要

We have previously reported that matador/Bcl-2 ovarian killer (Mtd/Bok), a proapoptotic member of the Bcl-2 family, regulates human trophoblast apoptosis and that its levels are elevated in severe preeclamptic pregnancy. Herein, we show that Mtd is also involved in the regulation of proliferation in normal and pathological placentae. Mtd was found in proliferating trophoblast cells during early placental development and in preeclampsia (PE). The main isoform of Mtd associated with trophoblast proliferation was Mtd-L, the full-length isoform, which preferentially localized to the nuclear compartment in proliferating cells, whereas during apoptosis it switched localization to the cytoplasm where it associated with mitochondria. Mtd expression in proliferating cells colocalized with cyclin E1, a G(1)/S phase cell cycle regulator. MtdL-specific knockdown in the early first trimester villous explants and in HEK293 revealed a direct effect of Mtd-L on cyclin E1 expression and cell cycle progression. We conclude that Mtd-L functions to regulate trophoblast cell proliferation during early placentation and that the elevated levels of Mtd found in PE may contribute to increased trophoblast proliferation accompanying this devastating disorder of pregnancy.
机译:我们以前曾报道过,斗牛士/ Bcl-2卵巢杀手(Mtd / Bok)是Bcl-2家族的促凋亡成员,它调节人滋养细胞凋亡,严重子痫前期妊娠时其水平升高。在本文中,我们显示Mtd也参与正常胎盘和病理胎盘中增殖的调节。 Mtd在胎盘早期发育和子痫前期(PE)的增生滋养细胞中发现。与滋养层细胞增殖有关的Mtd的主要同工型是全长同工型Mtd-L,其优先定位于增殖细胞的核区室,而在凋亡过程中,其将定位切换至与线粒体相关的胞质。 Mtd表达与cyclin E1,G(1)/ S期细胞周期调节剂共定位的增殖细胞中。 MtdL特异性敲低在早期的三个月绒毛外植体和HEK293中揭示了Mtd-L对细胞周期蛋白E1表达和细胞周期进程的直接影响。我们得出的结论是,Mtd-L的功能是在早期胎盘形成过程中调节滋养层细胞的增殖,而在PE中发现的Mtd升高的水平可能会导致这种破坏性妊娠疾病增加滋养层细胞的增殖。

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