Wächter Regula, Masarik Lukas, Bürzle Marc, Mallik Ajit, von Mandach Ursula
Department of Obstetrics, University Hospital Zurich, Zurich, Switzerland.
Fetal Diagn Ther. 2009;25(3):328-35. doi: 10.1159/000235879. Epub 2009 Sep 22.
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.
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.
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.
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.
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。
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。
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。
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。