The effects of tracheal occlusion on Wnt signaling in a rabbit model of congenital diaphragmatic hernia

• Published in: Journal of pediatric surgery Vol. 54; no. 5; pp. 937 - 944
• Main Authors: Mudri, Martina, Smith, Shane A., Vanderboor, Christina, Davidson, Jacob, Regnault, Timothy R.H., Bütter, Andreana
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-05-2019
• Subjects: Animal model; Congenital diaphragmatic hernia (CDH); Fetal surgery; Lgl1; miR-33; miR-375; Tracheal occlusion (TO); Wnt signaling; Wnt2; Animal model; Wnt signaling; Congenital diaphragmatic hernia (CDH); Tracheal occlusion (TO); Lgl1; miR-375; Fetal surgery; miR-33; Wnt2
• ISSN: 0022-3468; 1531-5037
• DOI: 10.1016/j.jpedsurg.2019.01.024

Tracheal occlusion (TO) reverses pulmonary hypoplasia (PH) in congenital diaphragmatic hernia (CDH), but its mechanism of action remains poorly understood. Wnt signaling plays a critical role in lung development, but few studies exist. The purpose of our study was to a) confirm that our CDH rabbit model produced PH which was reversed by TO and b) determine the effects of CDH +/− TO on Wnt signaling.
CDH was created in fetal rabbits at 23 days, TO at 28 days, and lung collection at 31 days. Lung body weight ratio (LBWR) and mean terminal bronchiole density (MTBD) were determined. mRNA and miRNA expression was determined in the left lower lobe using RT-qPCR.
Fifteen CDH, 15 CDH + TO, 6 sham CDH, and 15 controls survived and were included in the study. LBWR was low in CDH, while CDH + TO was similar to controls (p = 0.003). MTBD was higher in CDH fetuses and restored to control levels in CDH + TO (p < 0.001). Reference genes TOP1, SDHA, and ACTB were consistently expressed within and between treatment groups. miR-33 and MKI67 were increased, and Lgl1 was decreased in CDH + TO.
TO reversed pulmonary hypoplasia and stimulated early Wnt signaling in CDH fetal rabbits.
Basic science, prospective.
II.