Disruptions in airway branching or alveolar differentiation during lung development can lead to severe respiratory deficiencies and neonatal death. The molecular mechanisms governing branching patterning and early alveolar formation remain elusive. Loss of
Svep1
function in mice results in various developmental defects, including lung hypoplasia and perinatal lethality. Our examination of the lungs of
Svep1
knockout (
Svep1
-/-
)
mouse embryos, both
in vivo
and
in vitro
, revealed that
Svep1
mutants exhibit an increase in the number of disorganized distal airway tips and progressively greater disruption of lung lobe morphology over time and saccular development.
Svep1
interacts with FGF signaling to regulate smooth muscle differentiation and, together with
Fgf9,
guides airway branching patterning. Transcriptomic data from the lungs of
Svep1
-/-
embryos revealed dysregulated gene expression affecting saccular maturation. Our findings demonstrate that
Svep1
is a key extracellular matrix player shaping airway morphology and influencing alveolar fate. These insights offer potential avenues for therapeutic interventions in congenital lung disorders.