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YAP expression in endothelial cells prevents ventilator-induced lung injury.
Su, Kai; Wang, Jianguo; Lv, Yang; Tian, Ming; Zhao, You-Yang; Minshall, Richard D; Hu, Guochang.
Afiliação
  • Su K; Department of Anesthesiology, University of Illinois College of Medicine, Chicago, Illinois.
  • Wang J; Department of Anesthesiology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
  • Lv Y; Department of Anesthesiology, University of Illinois College of Medicine, Chicago, Illinois.
  • Tian M; Department of Anesthesiology, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Zhao YY; Department of Anesthesiology, University of Illinois College of Medicine, Chicago, Illinois.
  • Minshall RD; Department of Anesthesiology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
  • Hu G; Program for Lung and Vascular Biology, Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Am J Physiol Lung Cell Mol Physiol ; 320(4): L568-L582, 2021 04 01.
Article em En | MEDLINE | ID: mdl-33565367
ABSTRACT
Ventilator-induced lung injury is associated with an increase in mortality in patients with respiratory dysfunction, although mechanical ventilation is an essential intervention implemented in the intensive care unit. Intrinsic molecular mechanisms for minimizing lung inflammatory injury during mechanical ventilation remain poorly defined. We hypothesize that Yes-associated protein (YAP) expression in endothelial cells protects the lung against ventilator-induced injury. Wild-type and endothelial-specific YAP-deficient mice were subjected to a low (7 mL/kg) or high (21 mL/kg) tidal volume (VT) ventilation for 4 h. Infiltration of inflammatory cells into the lung, vascular permeability, lung histopathology, and the levels of inflammatory cytokines were measured. Here, we showed that mechanical ventilation with high VT upregulated YAP protein expression in pulmonary endothelial cells. Endothelial-specific YAP knockout mice following high VT ventilation exhibited increased neutrophil counts and protein content in bronchoalveolar lavage fluid, Evans blue leakage, and histological lung injury compared with wild-type littermate controls. Deletion of YAP in endothelial cells exaggerated vascular endothelial (VE)-cadherin phosphorylation, downregulation of vascular endothelial protein tyrosine phosphatase (VE-PTP), and dissociation of VE-cadherin and catenins following mechanical ventilation. Importantly, exogenous expression of wild-type VE-PTP in the pulmonary vasculature rescued YAP ablation-induced increases in neutrophil counts and protein content in bronchoalveolar lavage fluid, vascular leakage, and histological lung injury as well as VE-cadherin phosphorylation and dissociation from catenins following ventilation. These data demonstrate that YAP expression in endothelial cells suppresses lung inflammatory response and edema formation by modulating VE-PTP-mediated VE-cadherin phosphorylation and thus plays a protective role in ventilator-induced lung injury.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Permeabilidade Capilar / Endotélio Vascular / Proteínas Adaptadoras de Transdução de Sinal / Lesão Pulmonar Induzida por Ventilação Mecânica / Pulmão / Neutrófilos Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Assunto da revista: BIOLOGIA MOLECULAR / FISIOLOGIA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Permeabilidade Capilar / Endotélio Vascular / Proteínas Adaptadoras de Transdução de Sinal / Lesão Pulmonar Induzida por Ventilação Mecânica / Pulmão / Neutrófilos Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Assunto da revista: BIOLOGIA MOLECULAR / FISIOLOGIA Ano de publicação: 2021 Tipo de documento: Article