Endothelial tissue remodeling induced by intraluminal pressure enhances paracellular solute transport
Jean Cacheux,
Aurélien Bancaud,
Daniel Alcaide,
Jun-Ichi Suehiro,
Yoshihiro Akimoto,
Hiroyuki Sakurai,
Yukiko T. Matsunaga
Affiliations
Jean Cacheux
Institute of Industrial Science, The University of Tokyo, Tokyo 153-8505, Japan; LIMMS, CNRS-IIS UMI 2820, The University of Tokyo, Tokyo 153-8505, Japan
Aurélien Bancaud
Institute of Industrial Science, The University of Tokyo, Tokyo 153-8505, Japan; LIMMS, CNRS-IIS UMI 2820, The University of Tokyo, Tokyo 153-8505, Japan; CNRS, LAAS, 7 Avenue Du Colonel Roche, 31400 Toulouse, France; Corresponding author
Daniel Alcaide
Institute of Industrial Science, The University of Tokyo, Tokyo 153-8505, Japan
Jun-Ichi Suehiro
Department of Pharmacology and Toxicology, Kyorin University School of Medicine, 6-20-2, Shinkawa, Mitaka, Tokyo 181-8611, Japan
Yoshihiro Akimoto
Department of Anatomy, Kyorin University School of Medicine, Mitaka, Tokyo 181-8611, Japan
Hiroyuki Sakurai
Department of Pharmacology and Toxicology, Kyorin University School of Medicine, 6-20-2, Shinkawa, Mitaka, Tokyo 181-8611, Japan
Yukiko T. Matsunaga
Institute of Industrial Science, The University of Tokyo, Tokyo 153-8505, Japan; LIMMS, CNRS-IIS UMI 2820, The University of Tokyo, Tokyo 153-8505, Japan; Corresponding author
Summary: The endothelial layers of the microvasculature regulate the transport of solutes to the surrounding tissues. It remains unclear how this barrier function is affected by blood flow-induced intraluminal pressure. Using a 3D microvessel model, we compare the transport of macromolecules through endothelial tissues at mechanical rest or with intraluminal pressure, and correlate these data with electron microscopy of endothelial junctions. On application of an intraluminal pressure of 100 Pa, we demonstrate that the flow through the tissue increases by 2.35 times. This increase is associated with a 25% expansion of microvessel diameter, which leads to tissue remodeling and thinning of the paracellular junctions. We recapitulate these data with the deformable monopore model, in which the increase in paracellular transport is explained by the augmentation of the diffusion rate across thinned junctions under mechanical stress. We therefore suggest that the deformation of microvasculatures contributes to regulate their barrier function.
