Intra-vessel heterogeneity establishes enhanced sites of macromolecular leakage downstream of laminin α5

Endothelial cells display heterogeneous properties based on location and function. How this heterogeneity influences endothelial barrier stability both between and within vessel subtypes is unexplored. In this study, we find that endothelial cells exhibit heterogeneous barrier properties on inter-organ and intra-vessel levels. Using intravital microscopy and sequential stimulation of the ear dermis with vascular endothelial growth factor-A (VEGFA) and/or histamine, we observe distinct, reappearing sites, common for both agonists, where leakage preferentially takes place. Through repetitive stimulation of the diaphragm and trachea, we find inter-organ conservation of such predetermined leakage sites. Qualitatively, predetermined sites display distinct leakage properties and enhanced barrier breakdown compared to less susceptible regions. Mechanistically, laminin alpha 5 is reduced at predetermined sites, which is linked to reduced junctional vascular endothelial (VE)-cadherin and enhanced VEGFA-induced VE-cadherin phosphorylation. These data highlight functional intra-vessel heterogeneity that defines predetermined sites with distinct leakage properties and that may disproportionately impact pathological vascular leakage.

Automated summary

Endothelial cells exhibit heterogeneous barrier properties at inter-organ and intra-vessel levels, with predetermined leakage sites showing distinct characteristics that may disproportionately impact pathological vascular leakage. Mechanistically, reduced laminin alpha 5 at predetermined sites is associated with decreased VE-cadherin and increased VEGFA-induced VE-cadherin phosphorylation.