Fetal Tracheal Occlusion Correlates with Normalized YAP Expression and Alveolar Epithelial Differentiation in Congenital Diaphragmatic Hernia

Otros/as autores/as

Institut Català de la Salut

Aubert O] Division of Newborn Medicine, Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. Department of Pediatric Surgery, University Hospital Leipzig, Leipzig, Germany. [Miyake Y] Division of Pediatric Surgery, Department of Surgery, Rady Faculty of Health Sciences, Max Rady College of Medicine, University of Manitoba and Children’s Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada. [Amonkar GM, Dinwoodie OM] Division of Newborn Medicine, Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. [Varisco BM] College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. Arkansas Children’s Research Institute, Little Rock, Arkansas. [Marotta M] Grup de Recerca de Bioenginyeria, Teràpia Cel·lular i Cirurgia en Malformacions Congènites, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain

Vall d'Hebron Barcelona Hospital Campus

Fecha de publicación

2025-06-13T11:26:56Z

2025-06-13T11:26:56Z

2025-06



Resumen

Alveolar epithelial differentiation; Congenital diaphragmatic hernia; Fetal tracheal occlusion


Diferenciació epitelial alveolar; Hèrnia diafragmàtica congènita; Oclusió traqueal fetal


Diferenciación epitelial alveolar; Hernia diafragmática congénita; Oclusión traqueal fetal


Congenital diaphragmatic hernia (CDH) is characterized by incomplete closure of the diaphragm. Although the ensuing compression to the fetal lung causes lung hypoplasia, specific cellular phenotypes and developmental signaling defects in the alveolar epithelium in CDH are not fully understood. Employing lung samples from human CDH, a surgical lamb model, and a nitrofen rat model, we investigated whether lung compression impairs alveolar epithelial differentiation and Yes-associated protein (YAP)-mediated mechanosensing. We showed that CDH in humans and lambs caused defective alveolar epithelial differentiation manifested by more alveolar epithelial type II (ATII) cells, fewer ATI cells, and the emergence of cells coexpressing ATI and ATII markers. Associated with these alveolar epithelial defects, we found a decrease in the level and nuclear localization of YAP. Reduced YAP and abnormal distal lung development were evident as early as 21 weeks of gestation in human CDH. In addition, rat fetuses with CDH also showed diminished nuclear YAP and more abundant ATII cells. In contrast, the littermates without the hernia had no such alveolar phenotypes. Furthermore, fetal tracheal occlusion in the surgical lamb model of CDH fully normalized nuclear YAP and rescued alveolar epithelial defects in a gestational age-dependent manner. Taken together, our findings across species indicate that lung compression in CDH is sufficient to disrupt alveolar epithelial differentiation and impair YAP signaling. Tracheal occlusion can restore nuclear YAP and rescue the alveolar defects in CDH, depending on the timing and the duration of this prenatal surgical intervention.

Tipo de documento

Artículo


Versión publicada

Lengua

Inglés

Publicado por

American Thoracic Society

Documentos relacionados

American Journal of Respiratory Cell and Molecular Biology;72(6)

https://doi.org/10.1165/rcmb.2024-0323OC

Citación recomendada

Esta citación se ha generado automáticamente.

Derechos

Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

Este ítem aparece en la(s) siguiente(s) colección(ones)