Title: | Evidence for decreased lipofibroblast expression in hypoplastic rat lungs with congenital diaphragmatic hernia |
Author(s): | Friedmacher F; Fujiwara N; Hofmann AD; Takahashi H; Gosemann JH; Puri P; |
Address: | "National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin 12, Ireland, florian.friedmacher@gmx.de" |
DOI: | 10.1007/s00383-014-3549-z |
ISSN/ISBN: | 1437-9813 (Electronic) 0179-0358 (Linking) |
Abstract: | "PURPOSE: Pulmonary hypoplasia (PH) is a serious condition in newborns with congenital diaphragmatic hernia (CDH). Lipid-containing interstitial fibroblasts (LIFs) play an essential role in fetal lung maturation by stimulating alveolarization and lipid homeostasis. In rodents, LIFs are first evident during the canalicular phase of lung development with a significant increase over the last 4 days of gestation. Adipocyte differentiation-related protein (ADRP), a functional lipogenic molecular marker characterizing LIFs, is highly expressed in fetal lungs during this critical time period. We hypothesized that LIF expression in hypoplastic rat lungs is decreased in the nitrofen-induced CDH model, which is accompanied by reduced alveolar ADRP expression and lipid content. METHODS: On embryonic day 9.5 (E9.5), time-mated rats received either nitrofen or vehicle. Fetuses were sacrificed on selected time points E18.5 and E21.5, and dissected lungs were divided into controls and CDH-associated PH. Pulmonary gene expression levels of ADRP were determined by quantitative real-time polymerase chain reaction. ADRP immunohistochemistry and oil red O staining were used to assess pulmonary protein expression and lipid content. Immunofluorescence double staining for alpha smooth muscle actin, which is known to be absent in LIFs, and lipid droplets was performed to evaluate the pulmonary expression of this specific subset of fibroblasts. RESULTS: Relative mRNA expression of ADRP was significantly reduced in lungs of CDH-associated PH on E18.5 and E21.5 compared to controls. ADRP immunoreactivity and lipid staining were markedly diminished in alveolar mesenchymal cells of CDH-associated PH on E18.5 and E21.5 compared to controls. Confocal laser scanning microscopy demonstrated markedly decreased LIF expression in alveolar interstitium of CDH-associated PH on E18.5 and E21.5 compared to controls. CONCLUSION: Decreased pulmonary LIF expression during late gestation suggests impaired LIF functioning in the nitrofen-induced CDH model, which may cause disruption in fetal alveolarization and lipid homeostasis, and thus contribute to the development of PH" |
Keywords: | "Animals Disease Models, Animal Female Fetal Development/genetics Fibroblasts/*metabolism Gene Expression/genetics Gene Expression Regulation, Developmental/*genetics Hernias, Diaphragmatic, Congenital/*genetics Lung/*abnormalities/*embryology/metabolism M;" |
Notes: | "MedlineFriedmacher, Florian Fujiwara, Naho Hofmann, Alejandro Daniel Takahashi, Hiromizu Gosemann, Jan-Hendrik Puri, Prem eng Research Support, Non-U.S. Gov't Germany 2014/07/16 Pediatr Surg Int. 2014 Oct; 30(10):1023-9. doi: 10.1007/s00383-014-3549-z. Epub 2014 Jul 15" |