Novel Netrin-1-Unc5b-Klf4 axis balances AT2 survival in experimental bronchopulmonary dysplasia

Abstract Alveolar growth and repair are central processes in development and chronic lung disease, such as bronchopulmonary dysplasia (BPD), a neonatal lung disease without curative therapy. Alveolar epithelial type 2 cells (AT2) are the endogenous progenitor pool giving rise to AT1 and promoting alveolar repair. Since netrin-1, a regulator of cell homeostasis and stemness, has been linked to lung diseases, we now investigated its signaling and function in AT2 in a hyperoxia-based model of BPD and in lungs of infants with BPD. First, we demonstrated that prolonged hyperoxia reduced both netrin-1 and its receptor Unc5b in neonatal mouse lungs and in primary AT2 cells. Second, ex vivo studies using precision-cut lung slices (PCLS) and transgenic netrin-1 null mice showed that netrin-1 regulates AT2 survival and the expression of Krüppel-like factor 4 (Klf4) through Unc5b, a transcription factor regulating cell survival. Third, single cell and bulk transcriptomic analysis as well as proximity-dependent biotin identification assay, showed Klf4 to be upregulated in AT2 during alveolarization, downstream of netrin-1, and to regulate AT2 survival. In vivo, Klf4 gene expression and protein abundance was significantly reduced in total lung homogenates and in AT2 cells of neonatal mice exposed to hyperoxia. Finally, KLF4 + cells, KLF4 + epithelial, and specifically KLF4 + AT2 cells were reduced in clinical BPD. In summary, our data identify a novel netrin1-Unc5b-Klf4 axis in AT2 that is disrupted in BPD and could offer a novel target for endogenous alveolar repair.

Authors

Institutions

Publication Details

Journal
American Journal of Respiratory Cell and Molecular Biology
Published
2026-03-22
DOI
https://doi.org/10.1093/ajrcmb/aanag061
Primary Topic
Neonatal Respiratory Health Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Novel Netrin-1-Unc5b-Klf4 axis balances AT2 survival in experimental bronchopulmonary dysplasia

O Klymenko, Marek Bartkuhn, Dharmesh Hirani, Thomas Imhof et al.
American Journal of Respiratory Cell and Molecular Biology
Neonatal Respiratory Health Research
article

Novel Netrin-1-Unc5b-Klf4 axis balances AT2 survival in experimental bronchopulmonary dysplasia

O Klymenko, Marek Bartkuhn, Dharmesh Hirani, Thomas Imhof, Bernhard Schermer, Michele Donato, Jasmine Mohr, Christina Vohlen, Daniela Rheindorf, Cristina M. Alvira, Christoph Bartenhagen, Purvesh Khatri, Şerife Akgül, Lena K. Ebert, Soula Danopoulos, Stephanie Stephan, Stefan Müller, Miguel A Alejandre Alcázar, J Dötsch, T Procida, Theodoris Georgomanolis, Werner Seeger, Mohammad A Mahjoub, Ivana Mižík, Soni S Pullamsetti, Kerstin Goth, Manuel Koch, Celien Kuiper-Makris, Saverio Bellusci, Denise Al Alam, Ioannis Alexopoulos, Gloria S Pryhuber
article en

Abstract

Abstract Alveolar growth and repair are central processes in development and chronic lung disease, such as bronchopulmonary dysplasia (BPD), a neonatal lung disease without curative therapy. Alveolar epithelial type 2 cells (AT2) are the endogenous progenitor pool giving rise to AT1 and promoting alveolar repair. Since netrin-1, a regulator of cell homeostasis and stemness, has been linked to lung diseases, we now investigated its signaling and function in AT2 in a hyperoxia-based model of BPD and in lungs of infants with BPD. First, we demonstrated that prolonged hyperoxia reduced both netrin-1 and its receptor Unc5b in neonatal mouse lungs and in primary AT2 cells. Second, ex vivo studies using precision-cut lung slices (PCLS) and transgenic netrin-1 null mice showed that netrin-1 regulates AT2 survival and the expression of Krüppel-like factor 4 (Klf4) through Unc5b, a transcription factor regulating cell survival. Third, single cell and bulk transcriptomic analysis as well as proximity-dependent biotin identification assay, showed Klf4 to be upregulated in AT2 during alveolarization, downstream of netrin-1, and to regulate AT2 survival. In vivo, Klf4 gene expression and protein abundance was significantly reduced in total lung homogenates and in AT2 cells of neonatal mice exposed to hyperoxia. Finally, KLF4 + cells, KLF4 + epithelial, and specifically KLF4 + AT2 cells were reduced in clinical BPD. In summary, our data identify a novel netrin1-Unc5b-Klf4 axis in AT2 that is disrupted in BPD and could offer a novel target for endogenous alveolar repair.

American Journal of Respiratory Cell and Molecular Biology
University of Cologne (DE), UCLA Medical Center (US), University of Rochester Medical Center (US), German Center for Lung Research (DE), Universities of Giessen and Marburg Lung Center (DE), Stanford Medicine (US), Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (DE), University Hospital Cologne (DE), Cardio-Pulmonary Institute (DE), Institute of Infection and Immunity (CA), Harbor–UCLA Medical Center (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 8%
Neonatal Respiratory Health Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.