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首页> 外文期刊>Pediatric surgery international >Prenatal administration of retinoic acid upregulates connective tissue growth factor in the nitrofen CDH model.
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Prenatal administration of retinoic acid upregulates connective tissue growth factor in the nitrofen CDH model.

机译:产前给予视黄酸在硝基芬CDH模型中上调结缔组织生长因子。

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PURPOSE: Recent studies have suggested that retinoids may be involved in the molecular mechanisms of pulmonary hypoplasia (PH) in congenital diaphragmatic hernia (CDH). Connective tissue growth factor (CTGF) plays a key role in foetal lung development and remodelling during later gestation. CTGF knockout mice exhibit PH with similar characteristics to the human and nitrofen-induced PH. Prenatal administration of retinoic acid (RA) has been shown to stimulate alveologenesis in nitrofen-induced PH. In vitro studies have revealed that RA can induce CTGF gene expression. We hypothesized that pulmonary gene expression of CTGF is downregulated during the later stages of lung development, and that prenatal administration of RA upregulates CTGF in the nitrofen CDH model. METHODS: Pregnant rats were exposed to either olive oil or nitrofen on day 9 (D9) of gestation. RA was given intraperitoneally on D18, D19 and D20. Foetuses were harvested on D21 and divided into control, CDH, control + RA and CDH + RA group. Pulmonary CTGF gene and protein expression levels were determined using RT-PCR and immunohistochemistry. RESULTS: On D21, CTGF relative mRNA expression levels were significantly downregulated in CDH group compared to controls. After RA treatment, expression levels of CTGF were significantly upregulated in CDH + RA and control + RA compared to the CDH group. Immunohistochemical studies confirmed these results. CONCLUSION: Downregulation of pulmonary CTGF gene and protein expression during later stages of lung development may interfere with normal alveologenesis in the nitrofen CDH model. Upregulation of CTGF pulmonary gene expression after prenatal RA treatment may promote lung growth by promoting alveologenesis in the nitrofen-induced CDH model.
机译:目的:最近的研究表明,类维生素A可能参与了先天性diaphragm肌疝(CDH)的肺发育不全(PH)的分子机制。结缔组织生长因子(CTGF)在后期妊娠期间在胎儿肺部发育和重塑中起关键作用。 CTGF基因敲除小鼠表现出与人类和硝基苯酚诱导的PH具有相似特征的PH。视黄酸(RA)的产前给药已显示可刺激硝基苯酚诱导的PH中的肺泡生成。体外研究表明,RA可以诱导CTGF基因表达。我们假设在肺发育的后期,CTGF的肺基因表达被下调,而在硝基芬CDH模型中,产前服用RA会上调CTGF。方法:妊娠大鼠在妊娠的第9天(D9)暴露于橄榄油或硝基苯酚。在D18,D19和D20腹膜内给予RA。在D21上收获胎儿,并分为对照组,CDH,对照组+ RA和CDH + RA组。使用RT-PCR和免疫组织化学测定肺CTGF基因和蛋白质表达水平。结果:在D21,CDH组的CTGF相对mRNA表达水平明显低于对照组。 RA治疗后,与CDH组相比,CDH + RA和对照组+ RA中CTGF的表达水平显着上调。免疫组织化学研究证实了这些结果。结论:在肺部发育后期,肺CTGF基因和蛋白表达的下调可能会干扰硝基芬CDH模型的正常肺泡形成。产前RA治疗后CTGF肺基因表达的上调可能通过促进硝苯芬诱导的CDH模型中的肺泡生成来促进肺生长。

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