Literature DB >> 26096456

Neuroendocrine factors regulate retinoic acid receptors in normal and hypoplastic lung development.

Patrícia Pereira-Terra1,2, Rute S Moura1,2, Cristina Nogueira-Silva1,2,3, Jorge Correia-Pinto1,2,4.   

Abstract

KEY POINTS: Retinoic acid (RA) and ghrelin levels are altered in human hypoplastic lungs when compared to healthy lungs. Although considerable data have been obtained about RA, ghrelin and bombesin in the congenital diaphragmatic hernia (CDH) rat model, neuroendocrine factors have never been associated with the RA signalling pathway in this animal model. In this study, the interaction between neuroendocrine factors and RA was explored in the CDH rat model. The authors found that normal fetal lung explants treated with RA, bombesin and ghrelin showed an increase in lung growth. Hypoplastic lungs presented higher expression levels of the RA receptors α and γ. Moreover bombesin and ghrelin supplementation, in vitro, to normal lungs increased RA receptor α/γ expression whereas administration of bombesin and ghrelin antagonists to normal and hypoplastic lungs decreased it. These data reveal for the first time that there is a link between neuroendocrine factors and RA, and that neuroendocrine factors sensitise the lung to the RA action through RA receptor modulation. ABSTRACT: Congenital diaphragmatic hernia (CDH) is characterised by a spectrum of lung hypoplasia and consequent pulmonary hypertension, leading to high morbidity and mortality rates. Moreover, CDH has been associated with an increase in the levels of pulmonary neuroendocrine factors, such as bombesin and ghrelin, and a decrease in the action of retinoic acid (RA). The present study aimed to elucidate the interaction between neuroendocrine factors and RA. In vitro analyses were performed on Sprague-Dawley rat embryos. Normal lung explants were treated with bombesin, ghrelin, a bombesin antagonist, a ghrelin antagonist, dimethylsulfoxide (DMSO), RA dissolved in DMSO, bombesin plus RA and ghrelin plus RA. Hypoplastic lung explants (nitrofen model) were cultured with bombesin, ghrelin, bombesin antagonist or ghrelin antagonist. The lung explants were analysed morphometrically, and retinoic acid receptor (RAR) α, β and γ expression levels were assessed via Western blotting. Immunohistochemistry analysis of RAR was performed in normal and hypoplastic lungs 17.5 days post-conception (dpc). Compared with the controls, hypoplastic lungs exhibited significantly higher RARα/γ expression levels. Furthermore considering hypoplastic lungs, bombesin and ghrelin antagonists decreased RARα/γ expression. Normal lung explants (13.5 dpc) treated with RA, bombesin plus RA, ghrelin plus RA, bombesin or ghrelin exhibited increased lung growth. Moreover, bombesin and ghrelin increased RARα/γ expression levels, whereas the bombesin and ghrelin antagonists decreased RARα/γ expression. This study demonstrates for the first time that neuroendocrine factors function as lung growth regulators, sensitising the lung to the action of RA through up-regulation of RARα and RARγ.
© 2015 The Authors. The Journal of Physiology © 2015 The Physiological Society.

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Year:  2015        PMID: 26096456      PMCID: PMC4553054          DOI: 10.1113/JP270477

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  39 in total

1.  Bombesin inhibits apoptosis in developing fetal rat lung.

Authors:  M Kresch; C Christian; L Zhu; M Obe; M M Sanders; N Hussain
Journal:  Lung       Date:  1999       Impact factor: 2.584

2.  Immunohistochemical distribution of bombesin-positive pulmonary neuroendocrine cells in a congenital diaphragmatic hernia.

Authors:  K Asabe; K Tsuji; N Handa; M Kajiwara; S Suita
Journal:  Surg Today       Date:  1999       Impact factor: 2.549

3.  Vitamin A decreases the incidence and severity of nitrofen-induced congenital diaphragmatic hernia in rats.

Authors:  B Thébaud; D Tibboel; C Rambaud; J C Mercier; J R Bourbon; A T Dinh-Xuan; S L Archer
Journal:  Am J Physiol       Date:  1999-08

4.  The activation of the retinoic acid response element is inhibited in an animal model of congenital diaphragmatic hernia.

Authors:  Miao-hsueh Chen; Alice MacGowan; Simon Ward; Claes Bavik; John J Greer
Journal:  Biol Neonate       Date:  2003

5.  Retinol status of newborn infants with congenital diaphragmatic hernia.

Authors:  D Major; M Cadenas; L Fournier; S Leclerc; M Lefebvre; R Cloutier
Journal:  Pediatr Surg Int       Date:  1998-10       Impact factor: 1.827

6.  Electrophysiological evidence for the presence of receptors for cholecystokinin and bombesin on cultured astrocytes of rat central nervous system.

Authors:  L Hösli; E Hösli; T Winter; H Käser
Journal:  Neurosci Lett       Date:  1993-12-12       Impact factor: 3.046

7.  Prenatal treatment with retinoic acid accelerates type 1 alveolar cell proliferation of the hypoplastic lung in the nitrofen model of congenital diaphragmatic hernia.

Authors:  Kaoru Sugimoto; Hajime Takayasu; Nana Nakazawa; Sandra Montedonico; Prem Puri
Journal:  J Pediatr Surg       Date:  2008-02       Impact factor: 2.545

8.  Effects of maternal vitamin A status on fetal heart and lung: changes in expression of key developmental genes.

Authors:  C Antipatis; C J Ashworth; G Grant; R G Lea; S M Hay; W D Rees
Journal:  Am J Physiol       Date:  1998-12

9.  Reductions in the incidence of nitrofen-induced diaphragmatic hernia by vitamin A and retinoic acid.

Authors:  Randal P Babiuk; Bernard Thébaud; John J Greer
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2004-01-16       Impact factor: 5.464

10.  Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants.

Authors:  C Mendelsohn; D Lohnes; D Décimo; T Lufkin; M LeMeur; P Chambon; M Mark
Journal:  Development       Date:  1994-10       Impact factor: 6.868

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  8 in total

1.  Retinoic acid regulates avian lung branching through a molecular network.

Authors:  Hugo Fernandes-Silva; Patrícia Vaz-Cunha; Violina Baranauskaite Barbosa; Carla Silva-Gonçalves; Jorge Correia-Pinto; Rute Silva Moura
Journal:  Cell Mol Life Sci       Date:  2017-07-22       Impact factor: 9.261

Review 2.  Polygenic Causes of Congenital Diaphragmatic Hernia Produce Common Lung Pathologies.

Authors:  Patricia K Donahoe; Mauro Longoni; Frances A High
Journal:  Am J Pathol       Date:  2016-08-24       Impact factor: 4.307

3.  Transmural pressure signals through retinoic acid to regulate lung branching.

Authors:  Jacob M Jaslove; Katharine Goodwin; Aswin Sundarakrishnan; James W Spurlin; Sheng Mao; Andrej Košmrlj; Celeste M Nelson
Journal:  Development       Date:  2022-01-20       Impact factor: 6.862

Review 4.  Perinatal Undernutrition, Metabolic Hormones, and Lung Development.

Authors:  Juan Fandiño; Laura Toba; Lucas C González-Matías; Yolanda Diz-Chaves; Federico Mallo
Journal:  Nutrients       Date:  2019-11-23       Impact factor: 5.717

Review 5.  Developmental Pathways Underlying Lung Development and Congenital Lung Disorders.

Authors:  Inês Caldeira; Hugo Fernandes-Silva; Daniela Machado-Costa; Jorge Correia-Pinto; Rute Silva Moura
Journal:  Cells       Date:  2021-11-02       Impact factor: 6.600

6.  Distinct Epithelial Cell Profiles in Normal Versus Induced-Congenital Diaphragmatic Hernia Fetal Lungs.

Authors:  Ana N Gonçalves; Jorge Correia-Pinto; Cristina Nogueira-Silva
Journal:  Front Pediatr       Date:  2022-05-06       Impact factor: 3.418

Review 7.  Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

Authors:  Gabrielle Kardon; Kate G Ackerman; David J McCulley; Yufeng Shen; Julia Wynn; Linshan Shang; Eric Bogenschutz; Xin Sun; Wendy K Chung
Journal:  Dis Model Mech       Date:  2017-08-01       Impact factor: 5.758

Review 8.  Retinoic Acid: A Key Regulator of Lung Development.

Authors:  Hugo Fernandes-Silva; Henrique Araújo-Silva; Jorge Correia-Pinto; Rute S Moura
Journal:  Biomolecules       Date:  2020-01-17
  8 in total

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