...
首页> 外文期刊>Fetal diagnosis and therapy >Differential expression and activity of 11beta-hydroxysteroid dehydrogenase in human placenta and fetal membranes from pregnancies with intrauterine growth restriction.
【24h】

Differential expression and activity of 11beta-hydroxysteroid dehydrogenase in human placenta and fetal membranes from pregnancies with intrauterine growth restriction.

机译:胎儿宫内生长受限的人胎盘和胎膜中11β-羟类固醇脱氢酶的差异表达和活性。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVES: To study the expression and the function of the 11beta-hydroxysteroid dehydrogenase enzyme 1 (11beta-HSD1) and 2 (11beta-HSD2) in placenta and the fetal membranes from pregnancies with intrauterine growth restriction (IUGR) and from controls. METHODS: Amnion, chorion, decidua and cotyledon were separated from placenta; mRNA was analyzed by TaqMan real-time technology and proteins by Western blot; enzyme activities were measured by the conversion of 3H-cortisol to 3H-cortisone and vice versa. RESULTS: Predominant mRNA expression (p < 0.001) was found for 11beta-HSD1 in chorion and for 11beta-HSD2 in decidua and cotyledon. In pregnancies with IUGR, 11beta-HSD1 was upregulated in chorion (mean DeltaCt 11beta-HSD:18S mRNA 193.5 vs. 103.0 in controls respectively, p < 0.05) and 11beta-HSD2 was downregulated in decidua (mean DeltaCt 11beta-HSD2:18S mRNA 0.18 vs. 15.88 in controls respectively, p < 0.05). 11beta-HSD1 protein levels were reduced in amnion and 11beta-HSD1 and 11beta-HSD2 oxidase activity in decidua and cotyledon were reduced from pregnancies with IUGR. CONCLUSION: Reduced synthesis or activity of 11beta-HSD1 or 2 in cases of IUGR is shown in some but not in all tissues. The local mRNA expression of 11beta-HSD1 in chorion may reflect a mechanism on the post-transcriptional gene regulation to stimulate the formation of cortisone in IUGR. To provoke increasing activity with oxidase stimulators could be a future therapy in cases of IUGR.
机译:目的:研究11beta-羟类固醇脱氢酶1(11beta-HSD1)和2(11beta-HSD2)在胎盘和子宫内受胎儿宫内生长限制(IUGR)的胎膜和对照组中的表达和功能。方法:羊膜,绒毛膜,蜕膜和子叶与胎盘分离。通过TaqMan实时技术分析mRNA,通过Western blot分析蛋白质。通过将3H-皮质醇转化为3H-可的松来测量酶活性,反之亦然。结果:绒毛膜11beta-HSD1以及蜕膜和子叶11beta-HSD2的主要mRNA表达(p <0.001)。在IUGR妊娠中,绒毛膜中的11beta-HSD1上调(平均DeltaCt 11beta-HSD:18S mRNA 193.5比对照组的103.0,p <0.05),蜕膜中的11beta-HSD2下调(平均DeltaCt 11beta-HSD2:18S mRNA)对照分别为0.18和15.88,p <0.05)。 IUGR孕妇的羊膜中11beta-HSD1蛋白水平降低,蜕膜和子叶中11beta-HSD1和11beta-HSD2氧化酶活性降低。结论:在部分而非全部组织中,在IUGR中显示出11beta-HSD1或2的合成或活性降低。绒毛膜中11beta-HSD1的局部mRNA表达可能反映了转录后基因调控刺激IUGR中可的松形成的机制。在IUGR的情况下,用氧化酶刺激剂激发增加的活性可能是未来的治疗方法。

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