J Pediatr Surg
. 2024 Jul 30:161656.
doi: 10.1016/j.jpedsurg.2024.07.041. Online ahead of print. https://pubmed.ncbi.nlm.nih.gov/39181781/
Comparative Transcriptome Analysis of Human and Mouse Canalicular Lungs in Fetal Diaphragmatic Hernia
Shelby R Sferra 1, Juan C Biancotti 1, Raheel Ahmad 1, Anne M Sescleifer 1, Ciaran R Bubb 1, Mark L Kovler 1, Shaun M Kunisaki 2
Affiliations Expand
- PMID: 39181781
- DOI: 10.1016/j.jpedsurg.2024.07.041
Abstract
Background: The nitrofen model of congenital diaphragmatic hernia (CDH) is widely used in translational research. However, the molecular pathways associated with pulmonary hypoplasia in this model compared to the human CDH phenotype have not been well described. The aim of this study was to investigate differentially expressed genes (DEG) and signaling pathways in early stage fetal lungs in mouse and human CDH.
Methods: CDH lung tissue was obtained from human fetuses (21-23 weeks gestation) and nitrofen mouse pups (E15.5). NovaSeq Flowcell RNA-seq was performed to evaluate differentially expressed transcriptional and molecular pathways (DEGs) in fetal mice with CDH, compared with age-matched normal mouse lungs and human CDH samples.
Results: There were thirteen overlapping DEGs in human and mouse CDH lung samples compared to controls. These genes were involved in extracellular matrix, myogenesis, cilia, and immune modulation pathways. Human CDH was associated with an upregulation of collagen formation and extracellular matrix reorganization whereas mouse CDH was associated with an increase in muscular contraction. The most common cell types upregulated in human and mouse CDH samples were ciliated airway cells.
Conclusions: This study highlights the unique gene transcriptional patterns in early fetal mouse and human lungs with CDH. These data have implications when determining the translational potential of novel therapies in CDH using nitrofen-based animal models.
Level of evidence: Level IV.
Study type: Basic science/case series.
Keywords: Animal model; Congenital diaphragmatic hernia; Fetal surgery; Transcriptome analysis.
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