Link: https://www.ncbi.nlm.nih.gov/pubmed/30792093

J Pediatr Surg. 2019 Jan 31. pii: S0022-3468(19)30061-2. doi: 10.1016/j.jpedsurg.2019.01.024. [Epub ahead of print]
The effects of tracheal occlusion on Wnt signaling in a rabbit model of congenital diaphragmatic hernia.
Mudri M1, Smith SA1, Vanderboor C2, Davidson J3, Regnault TRH2, Bütter A4.
Author information
Abstract
PURPOSE:
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.

METHODS:
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.

RESULTS:
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.

CONCLUSION:
TO reversed pulmonary hypoplasia and stimulated early Wnt signaling in CDH fetal rabbits.

TYPE OF STUDY:
Basic science, prospective.

LEVEL OF EVIDENCE:
II.

Copyright © 2019 Elsevier Inc. All rights reserved.

KEYWORDS:
Animal model; Congenital diaphragmatic hernia (CDH); Fetal surgery; Lgl1; Tracheal occlusion (TO); Wnt signaling; Wnt2; miR-33; miR-375

PMID: 30792093 DOI: 10.1016/j.jpedsurg.2019.01.024
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