Bronchopulmonary Dysplasia with Pulmonary Hypertension Associates with Loss of Semaphorin Signaling and Functional Decrease in FOXF1 Expression

Author:

Shirazi Shawyon P.,Negretti Nicholas M.ORCID,Jetter Christopher S.,Sharkey Alexandria L.,Garg Shriya,Kapp Meghan E.,Wilkins Devan,Fortier Gabrielle,Mallapragada Saahithi,Banovich Nicholas E.,Wright Christopher V. E.,Frank David B.,Kropski Jonathan A.ORCID,Sucre Jennifer M. S.ORCID

Abstract

AbstractLung injury in preterm infants leads to structural and functional respiratory deficits, with a risk for bronchopulmonary dysplasia (BPD) that in its most severe form is accompanied by pulmonary hypertension (PH). To examine cellular and molecular dynamics driving evolving BPD in humans, we performed single-cell RNA sequencing of preterm infant lungs in early stages of BPD and BPD+PH compared to term infants. Analysis of the endothelium revealed a unique aberrant capillary cell-state primarily in BPD+PH marked byANKRD1expression. Predictive signaling analysis identified deficits in the semaphorin guidance-cue signaling pathway and decreased expression of pro-angiogenic transcription factorFOXF1within the alveolar parenchyma in neonatal lung samples with BPD/BPD+PH. Loss of semaphorin signaling was replicated in a murine BPD model and in humans with alveolar capillary dysplasia (ACDMPV), suggesting a mechanistic link between the developmental programs underlying BPD and ACDMPV and a critical role for semaphorin signaling in normal lung development.

Publisher

Cold Spring Harbor Laboratory

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