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正常及生长受限的人类妊娠中胎盘碘甲状腺原氨酸脱碘酶的表达

Placental iodothyronine deiodinase expression in normal and growth-restricted human pregnancies.

作者信息

Chan S, Kachilele S, Hobbs E, Bulmer J N, Boelaert K, McCabe C J, Driver P M, Bradwell A R, Kester M, Visser T J, Franklyn J A, Kilby M D

机构信息

Department of Fetal Medicine, Division of Reproductive and Child Health, University of Birmingham, Birmingham, United Kingdom B15 2TG.

出版信息

J Clin Endocrinol Metab. 2003 Sep;88(9):4488-95. doi: 10.1210/jc.2003-030228.

Abstract

We have described the expression of specific iodothyronine deiodinase mRNAs (using quantitative RT-PCR) and activities in normal human placentas throughout gestation and compared our findings to those in placentas from pregnancies affected by intrauterine growth restriction (IUGR). The predominant deiodinase expressed in placenta was type III (D3); type II (D2) was also present. In general terms, the activities of the enzymes D2 and D3 (and mRNAs encoding these enzymes) were higher earlier in gestation (<28 wk) than at term and displayed an inverse relationship with the duration of gestation (P < 0.05). Comparison of the relative expressions of mRNAs encoding D2 and D3 as well as their activities in placentas associated with IUGR (early and late gestational groups) with findings from normal placentas of similar gestational ages revealed no significant differences. Immunolocalization of D2 and D3 in syncytiotrophoblast (including syncytial sprouts) and cytotrophoblast of human placentas was demonstrated at both early and late gestation. Treatment of primary cultures of term cytotrophoblast cells in vitro with increasing doses of T(3) (1, 10, and 100 nM) resulted in increased expression of mRNAs encoding both D2 and D3 at 100-nM concentrations (P < 0.01) compared with control. Experiments with JEG-3 choriocarcinoma cells demonstrated a similar effect on D3 mRNA at 10 and 100 nM T(3) (P < 0.01). The demonstrated changes in iodothyronine deiodinase expression in the placenta across pregnancy are likely to contribute to regulation of the thyroid hormone supply to the developing fetus. The lack of difference in deiodinase expression in normal placentas and those found in IUGR argues against placental deiodinases being responsible for the hypothyroxemia in circulating fetal thyroid hormones observed in this condition.

摘要

我们描述了整个孕期正常人类胎盘中特定碘甲状腺原氨酸脱碘酶mRNA的表达(使用定量逆转录聚合酶链反应)及活性,并将我们的研究结果与宫内生长受限(IUGR)妊娠胎盘的结果进行了比较。胎盘中表达的主要脱碘酶是III型(D3);II型(D2)也存在。一般而言,D2和D3酶(以及编码这些酶的mRNA)的活性在妊娠早期(<28周)高于足月时,且与妊娠持续时间呈负相关(P<0.05)。将IUGR相关胎盘(妊娠早期和晚期组)中编码D2和D3的mRNA的相对表达及其活性与相似孕周正常胎盘的结果进行比较,未发现显著差异。在妊娠早期和晚期均证实了人胎盘合体滋养层(包括合体滋养层芽)和细胞滋养层中D2和D3的免疫定位。用递增剂量的T(3)(1、10和100 nM)体外处理足月细胞滋养层细胞原代培养物,与对照组相比,在100 nM浓度下导致编码D2和D3的mRNA表达增加(P<0.01)。用JEG-3绒毛膜癌细胞进行的实验表明,在10和100 nM T(3)时对D3 mRNA有类似影响(P<0.01)。整个孕期胎盘中碘甲状腺原氨酸脱碘酶表达的变化可能有助于调节向发育中胎儿的甲状腺激素供应。正常胎盘和IUGR胎盘中脱碘酶表达缺乏差异,这表明胎盘脱碘酶不是导致这种情况下循环胎儿甲状腺激素甲状腺功能减退的原因。

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