Endothelial cell Piezo1 mediates pressure-induced lung vascular hyperpermeability via disruption of adherens junctions
Author(s) -
Emily E. Friedrich,
Zhigang Hong,
Shiqin Xiong,
Ming Zhong,
Anke Di,
Jalees Rehman,
Yulia Komarova,
Asrar B. Malik
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1902165116
Subject(s) - adherens junction , piezo1 , pulmonary edema , hydrostatic pressure , lung , endothelial stem cell , edema , vascular permeability , endothelium , medicine , tight junction , ve cadherin , microbiology and biotechnology , pathology , chemistry , biology , cell , cadherin , biochemistry , mechanosensitive channels , ion channel , receptor , in vitro , physics , thermodynamics
Significance Increased hydrostatic pressure in lung capillaries experienced during high altitude, head trauma, and left heart failure can lead to disruption of lung endothelial barrier and edema formation. We identified Piezo1 as a mechanical sensor responsible for endothelial barrier breakdown (barotrauma) secondary to reduced expression of the endothelial adherens junction proteins VE-cadherin, β-catenin, and p120-catenin. Endothelial-specific deletion or pharmacological inhibition of Piezo1 prevented lung capillary leakage, suggesting a therapeutic approach for preventing edema and associated lung failure.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom