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Estrogen-Enhanced Gene Expression of Lipoprotein Lipase in Heart Is Antagonized by Progesterone

机译:孕酮拮抗心脏中脂蛋白脂肪酶的雌激素增强基因表达

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摘要

Although estrogen has effects on the heart, little is known regarding which genes in the heart are directly responsive to estrogen. We have shown previously that lipoprotein lipase (LPL) expression was increased in female hearts compared with male hearts. To test whether LPL gene expression in heart is regulated by estrogen, we perfused mouse hearts from ovariectomized females with 100 nM 17β-estradiol or vehicle for 2 h, after which hearts were frozen, and RNA was isolated. The SYBR green real-time PCR method was used to detect LPL gene expression. We found that addition of 17β-estradiol to hearts from ovariectomized females resulted in a significant increase in LPL mRNA. This estrogen effect on LPL gene expression in mouse heart can be blocked by the estrogen receptor (ER) antagonist ICI 182,780 or by progesterone. We also identified a potential estrogen receptor element (ERE) enhancer sequence located in the first intron of the mouse LPL gene. The potential ERE sequence was linked to a TATA-luciferase (LUC) reporter plasmid in HeLa cells. Both ERα and ERβ stimulated strong activity on the heterologous promoter reporter in Hela cells upon estrogen addition. Both ERα and ERβ activities on the LPL ERE reporter were abrogated by the ER antagonist ICI 182,780. Progesterone also dose dependently inhibited the estrogen-mediated increase in LPL ERE reporter activity. These results show that heart LPL is an estrogen-responsive gene exhibiting an intronic regulatory sequence.
机译:尽管雌激素对心脏有影响,但关于心脏中哪些基因直接对雌激素起反应的知之甚少。先前我们已经证明,与男性心脏相比,女性心脏中脂蛋白脂肪酶(LPL)的表达增加了。为了测试心脏中LPL基因的表达是否受到雌激素的调节,我们用100 nM17β-雌二醇或溶媒对来自卵巢切除的雌性小鼠的心脏进行了2 h的灌注,然后冷冻并分离了RNA。 SYBR绿色实时PCR方法用于检测LPL基因表达。我们发现从卵巢切除的女性的心脏中添加17β-雌二醇会导致LPL mRNA的显着增加。雌激素受体(ER)拮抗剂ICI 182,780或孕激素可阻断这种对小鼠心脏中LPL基因表达的雌激素作用。我们还确定了潜在的雌激素受体元件(ERE)增强子序列位于小鼠LPL基因的第一个内含子。潜在的ERE序列与HeLa细胞中的TATA荧光素酶(LUC)报告质粒相连。加入雌激素后,ERα和ERβ都对Hela细胞中的异源启动子报告子刺激了很强的活性。 ER拮抗剂ICI 182,780废除了LPL ERE报告基因上的ERα和ERβ活性。孕酮还剂量依赖性地抑制了雌激素介导的LPL ERE报告基因活性的增加。这些结果表明,心脏LPL是显示内含子调节序列的雌激素响应基因。

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