Lats1/2 Are Essential for Developmental Vascular Remodeling and Biomechanical Adaptation to Shear Stress.

Authors

Mitzy A Cowdin, Tuli Pramanik, Shelby R Mohr-Allen, Yuting Fu, Austin Mills, Stephen B Spurgin, Victor D Varner, George E Davis, Ondine Cleaver

Published in

Arteriosclerosis, thrombosis, and vascular biology. Jun 12, 2025. Epub Jun 12, 2025.

Abstract

Mechanical cues exerted by shear stress from blood flow remodel an initial vascular plexus into a ramifying array of large and small vessels. Hemodynamic forces trigger changes in endothelial cell (EC) gene expression and dynamic alterations in cell shape and adhesion. The objective of this study is to elucidate the role of the Lats (large tumor suppressor) 1 and Lats2 (Lats1/2) Hippo pathway kinases in EC transducing of hemodynamic signals as vessels form.
Lats1/2 were genetically deleted in murine ECs (Lats^iECDKO) and developing vessels were evaluated using immunofluorescence. Primary human pulmonary artery ECs were used to model endothelial response to blood flow and Lats1/2 depletion was achieved via siRNA treatment. EC junctions, cytoskeletal rearrangements, cell shape, and polarization were assessed using immunofluorescence. mRNA expression analyses and Western blotting were performed to understand changes in the response to shear stress in cultured ECs.
We report a critical requirement for Lats1/2 in adapting to blood flow during vascular development. When Lats1/2 are genetically deleted in ECs, embryos develop severe defects in blood vessel formation, which lead to embryonic lethality by embryonic day 11.5. Vessel patterning and circulation initiate properly; however, remodeling of the initial vascular plexus fails due to lumen collapse. Lats1/2 depletion in cultured ECs leads to failed polarization, elongation, and VEcad (vascular endothelial cadherin 5) junctional maturation underflow. Finally, YAP (Yes-associated protein)/TAZ (transcriptional coactivator with PDZ-binding motif) codepletion in Lats1/2 depleted conditions leads to a partial rescue of phenotypes in vivo and in vitro.
Our results suggest that Lats1/2 deficient cells no longer respond to laminar shear stress, in vivo and in vitro. This work identifies Lats1 and Lats2 as critical transducers of biomechanical cues during early blood vessel remodeling. This study provides new targets for treating vascular diseases and new directions for efforts to generate vascularized tissues for replacement therapies.

PMID:
40501385
Bibliographic data and abstract were imported from PubMed on 12 Jun 2025.

Read full publication at:
Please sign in to see all details.

Stats

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.