Barrier Enhancing Signals in Pulmonary Edema

被引:45
作者
Birukov, Konstantin G. [1 ]
Zebda, Noureddine [1 ]
Birukova, Anna A. [1 ]
机构
[1] Univ Chicago, Dept Med, Sect Pulm & Crit Care, Lung Injury Ctr, Chicago, IL 60637 USA
关键词
KERATINOCYTE GROWTH-FACTOR; ACTIVATED PROTEIN-C; ATRIAL-NATRIURETIC-PEPTIDE; ACUTE LUNG INJURY; VASCULAR-ENDOTHELIAL-CADHERIN; LIGHT-CHAIN KINASE; FOCAL ADHESION KINASE; CELL-CELL ADHESION; VASODILATOR-STIMULATED PHOSPHOPROTEIN; ALVEOLAR EPITHELIAL REPAIR;
D O I
10.1002/cphy.c100066
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Increased endothelial permeability and reduction of alveolar liquid clearance capacity are two leading pathogenic mechanisms of pulmonary edema, which is a major complication of acute lung injury, severe pneumonia, and acute respiratory distress syndrome, the pathologies characterized by unacceptably high rates of morbidity and mortality. Besides the success in protective ventilation strategies, no efficient pharmacological approaches exist to treat this devastating condition. Understanding of fundamental mechanisms involved in regulation of endothelial permeability is essential for development of barrier protective therapeutic strategies. Ongoing studies characterized specific barrier protective mechanisms and identified intracellular targets directly involved in regulation of endothelial permeability. Growing evidence suggests that, although each protective agonist triggers a unique pattern of signaling pathways, selected common mechanisms contributing to endothelial barrier protection may be shared by different barrier protective agents. Therefore, understanding of basic barrier protective mechanisms in pulmonary endothelium is essential for selection of optimal treatment of pulmonary edema of different etiology. This article focuses on mechanisms of lung vascular permeability, reviews major intracellular signaling cascades involved in endothelial monolayer barrier preservation and summarizes a current knowledge regarding recently identified compounds which either reduce pulmonary endothelial barrier disruption and hyperpermeability, or reverse preexisting lung vascular barrier compromise induced by pathologic insults. (C) 2013 American Physiological Society. Compr Physiol 3:429-484, 2013.
引用
收藏
页码:429 / 484
页数:56
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