Literature DB >> 21986617

Smad1 and WIF1 genes are downregulated during saccular stage of lung development in the nitrofen rat model.

Naho Fujiwara1, Takashi Doi, Jan-Hendrik Gosemann, Balazs Kutasy, Florian Friedmacher, Prem Puri.   

Abstract

PURPOSE: The exact pathogenesis of pulmonary hypoplasia in the nitrofen-induced congenital diaphragmatic hernia (CDH) still remains unclear. Smad1, one of the bone morphogenesis protein (BMP) receptor downstream signaling proteins, plays a key role in organogenesis including lung development and maturation. Smad1 knockout mice display reduced sacculation, an important feature of pulmonary hypoplasia. Wnt inhibitor factor 1 (Wif1) is a target gene of Smad1 in the developing lung epithelial cells (LECs). Smad1 directly regulates Wif1 gene expression and blockade of Smad1 function in fetal LECs is reported to downregulate Wif1 gene expression. We designed this study to test the hypothesis that pulmonary Smad1 and Wif1 gene expression is downregulated during saccular stage of lung development in the nitrofen CDH model.
METHODS: Pregnant rats were exposed to either olive oil or nitrofen on day 9 of gestation (D9). Fetuses were harvested on D18, and D21. Fetal lungs were dissected and divided into 2 groups: control and nitrofen (n = 9 at each time point, respectively). Pulmonary gene expression of Smad1 and Wif1 were analyzed by real-time RT-PCR. Immunohistochemistry was performed to evaluate protein expression/distribution of Smad1 and Wif1.
RESULTS: The relative mRNA expression levels of Smad1 and Wif1 were significantly downregulated in the nitrofen group compared to controls on D18 and D21 (*p < 0.01, **p < 0.05). Immunoreactivity of Smad1 and Wif1 was also markedly decreased in nitrofen lungs compared to controls on D18 and D21.
CONCLUSION: We provide evidence, for the first time, that the pulmonary gene expression of Smad1 and Wif1 is downregulated on D18 and D21 (saccular stage of lung development) in the nitrofen-induced hypoplastic lung. These findings suggest that the downregulation of Smad1/Wif1 gene expression may contribute to pulmonary hypoplasia in the nitrofen CDH model by retardation of lung development during saccular stage.

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Year:  2012        PMID: 21986617     DOI: 10.1007/s00383-011-2987-0

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  20 in total

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2.  Smad1 and its target gene Wif1 coordinate BMP and Wnt signaling activities to regulate fetal lung development.

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3.  Expression of Smad1 and Smad2 during embryogenesis suggests a role in organ development.

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4.  Nitrofen-induced diaphragmatic hernias in rats: an animal model.

Authors:  D Kluth; R Kangah; P Reich; R Tenbrinck; D Tibboel; W Lambrecht
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5.  Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.

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8.  Prenatal treatment with retinoic acid activates parathyroid hormone-related protein signaling in the nitrofen-induced hypoplastic lung.

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Journal:  Pediatr Surg Int       Date:  2011-01       Impact factor: 1.827

Review 9.  Congenital diaphragmatic hernia: searching for answers.

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1.  Downregulated bone morphogenetic protein signaling in nitrofen-induced congenital diaphragmatic hernia.

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4.  Pulmonary transcriptome analysis in the surgically induced rabbit model of diaphragmatic hernia treated with fetal tracheal occlusion.

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