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Peroxisome Proliferator-Activated Receptors Alpha, Beta, and Gamma mRNA and Protein Expression in Human Fetal Tissues

机译:人胎儿组织中过氧化物酶体增殖物激活的受体α,β和γmRNA和蛋白表达

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Peroxisome proliferator-activated receptors (PPARs) regulate lipid and glucose homeostasis, are targets of pharmaceuticals, and are also activated by environmental contaminants. Almost nothing is known about expression of PPARs during human fetal development. This study examines expression of PPARα,β, andγmRNA and protein in human fetal tissues. With increasing fetal age, mRNA expression of PPARαandβincreased in liver, but PPARβdecreased in heart and intestine, and PPARγdecreased in adrenal. Adult and fetal mean expression of PPARα,β, andγmRNA did not differ in intestine, but expression was lower in fetal stomach and heart. PPARαandβmRNA in kidney and spleen, and PPARγmRNA in lung and adrenal were lower in fetal versus adult. PPARγin liver and PPARβmRNA in thymus were higher in fetal versus adult. PPARαprotein increased with fetal age in intestine and decreased in lung, kidney, and adrenal. PPARβprotein in adrenal and PPARγin kidney decreased with fetal age. This study provides new information on expression of PPAR subtypes during human development and will be important in evaluating the potential for the developing human to respond to PPAR environmental or pharmaceutical agonists.
机译:过氧化物酶体增殖物激活受体(PPAR)调节脂质和葡萄糖的体内稳态,是药物的靶标,并且也被环境污染物激活。关于人类胎儿发育过程中PPAR的表达几乎一无所知。这项研究检查了人类胎儿组织中PPARα,β和γmRNA和蛋白质的表达。随着胎儿年龄的增长,肝脏中PPARα和β的mRNA表达增加,而心脏和肠中PPARβ的表达减少,肾上腺中PPARγ的表达减少。 PPARα,β和γmRNA的成人和胎儿平均表达在肠道中没有差异,但在胎儿胃和心脏中较低。胎儿和成人的肾脏和脾脏中的PPARα和βmRNA以及肺和肾上腺中的PPARγmRNA较低。与成人相比,胎儿中肝脏中的PPARγ和胸腺中的PPARβmRNA较高。 PPARα蛋白随着胎儿在肠道中的年龄而增加,而在肺,肾和肾上腺中则降低。肾上腺中的PPARβ蛋白和肾中的PPARγ随胎儿年龄而降低。这项研究提供了有关人类发育过程中PPAR亚型表达的新信息,对于评估发育中的人类对PPAR环境或药物激动剂的反应潜力具有重要意义。

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