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11β-羟类固醇脱氢酶在宫内生长受限妊娠的人胎盘和胎膜中的差异表达及活性

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

作者信息

Wächter Regula, Masarik Lukas, Bürzle Marc, Mallik Ajit, von Mandach Ursula

机构信息

Department of Obstetrics, University Hospital Zurich, Zurich, Switzerland.

出版信息

Fetal Diagn Ther. 2009;25(3):328-35. doi: 10.1159/000235879. Epub 2009 Sep 22.

Abstract

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.

摘要

目的

研究11β-羟基类固醇脱氢酶1(11β-HSD1)和2(11β-HSD2)在宫内生长受限(IUGR)妊娠及对照妊娠的胎盘和胎膜中的表达及功能。

方法

从胎盘中分离出羊膜、绒毛膜、蜕膜和子叶;采用TaqMan实时技术分析mRNA,采用蛋白质印迹法分析蛋白质;通过3H-皮质醇向3H-可的松的转化及反之的转化来测定酶活性。

结果

绒毛膜中11β-HSD1的mRNA表达占优势(p<0.001),蜕膜和子叶中11β-HSD2的mRNA表达占优势。在IUGR妊娠中,绒毛膜中11β-HSD1上调(11β-HSD:18S mRNA的平均ΔCt分别为193.5和对照中的103.0,p<0.05),蜕膜中11β-HSD2下调(11β-HSD2:18S mRNA的平均ΔCt分别为0.18和对照中的15.88,p<0.05)。IUGR妊娠中羊膜中11β-HSD1蛋白水平降低,蜕膜和子叶中11β-HSD1和11β-HSD2氧化酶活性降低。

结论

IUGR病例中部分而非所有组织显示11β-HSD1或2的合成或活性降低。绒毛膜中11β-HSD1的局部mRNA表达可能反映了转录后基因调控机制,以刺激IUGR中可的松的形成。用氧化酶刺激剂激发活性增加可能是IUGR病例未来的治疗方法。

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