Dingemann Jens, Doi Takashi, Ruttenstock Elke, Puri Prem
The Children's Research Centre, Our Lady's Children's Hospital, Dublin 12, Ireland.
Pediatr Surg Int. 2010 Jan;26(1):65-9. doi: 10.1007/s00383-009-2514-8.
Pulmonary hypoplasia and persistent pulmonary hypertension (PPH) aggravate clinical courses in congenital diaphragmatic hernia (CDH). Endothelin 1 enhances PPH by vasoconstriction and proliferation of vessel walls. Up-regulation of pulmonary Endothelin Receptors A and B (EDNRA, EDNRB) has been reported in human CDH and animal models, but the onset of those alterations during lung development remains unclear. We hypothesized that pulmonary expression of EDNRA and EDNRB is up-regulated at early gestational stages in the nitrofen model.
Pregnant rats were exposed to nitrofen or vehicle on gestational day 9 (D9). Embryos were sacrificed on D15, D18 and D21 and divided into nitrofen- and control group. Pulmonary RNA was extracted and mRNA levels of EDNRA and EDNRB were determined by real-time PCR. Immunohistochemistry for protein expression of both receptors was performed.
mRNA levels of EDNRA and EDNRB were significantly increased in the nitrofen group on D15, D18 and D21. Immunohistochemistry revealed increased pulmonary vascular expression of EDNRA and EDNRB compared to controls.
Altered expression of EDNRA and EDNRB is an early event in lung morphogenesis in the nitrofen model. We speculate that pulmonary arteries in CDH become excessively muscularised in early fetal life, becoming unable to adapt normally at birth.
肺发育不全和持续性肺动脉高压(PPH)会加重先天性膈疝(CDH)的临床病程。内皮素1通过血管收缩和血管壁增殖加重PPH。在人类CDH和动物模型中,已报道肺内皮素受体A和B(EDNRA、EDNRB)上调,但这些改变在肺发育过程中的起始情况仍不清楚。我们假设在孕早期,在硝基芬模型中EDNRA和EDNRB的肺表达会上调。
在妊娠第9天(D9)给怀孕大鼠暴露于硝基芬或赋形剂。在D15、D18和D21处死胚胎,并分为硝基芬组和对照组。提取肺RNA,通过实时PCR测定EDNRA和EDNRB的mRNA水平。对两种受体的蛋白表达进行免疫组织化学检测。
在D15、D18和D21,硝基芬组中EDNRA和EDNRB的mRNA水平显著升高。免疫组织化学显示,与对照组相比,EDNRA和EDNRB的肺血管表达增加。
在硝基芬模型中,EDNRA和EDNRB表达改变是肺形态发生的早期事件。我们推测,CDH中的肺动脉在胎儿早期过度肌化,导致出生时无法正常适应。