Mechanosensing and Mechanoregulation of Endothelial Cell Functions

被引:74
作者
Fang, Yun [1 ]
Wu, David [1 ]
Birukov, Konstantin G. [2 ]
机构
[1] Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[2] Univ Maryland, Sch Med, Dept Anesthesiol, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
SMOOTH-MUSCLE-CELLS; HEPATOCYTE GROWTH-FACTOR; FOCAL ADHESION KINASE; KRUPPEL-LIKE FACTOR-2; NF-KAPPA-B; HEMODYNAMIC SHEAR-STRESS; MONOCYTE CHEMOATTRACTANT PROTEIN-1; STRETCH-INDUCED APOPTOSIS; RHO-FAMILY GTPASES; HEPARAN-SULFATE PROTEOGLYCANS;
D O I
10.1002/cphy.c180020
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Vascular endothelial cells (ECs) form a semiselective barrier for macromolecules and cell elements regulated by dynamic interactions between cytoskeletal elements and cell adhesion complexes. ECs also participate in many other vital processes including innate immune reactions, vascular repair, secretion, and metabolism of bioactive molecules. Moreover, vascular ECs represent a unique cell type exposed to continuous, time-dependent mechanical forces: different patterns of shear stress imposed by blood flow in macrovasculature and by rolling blood cells in the microvasculature; circumferential cyclic stretch experienced by the arterial vascular bed caused by heart propulsions; mechanical stretch of lung microvascular endothelium at different magnitudes due to spontaneous respiration or mechanical ventilation in critically ill patients. Accumulating evidence suggests that vascular ECs contain mechanosensory complexes, which rapidly react to changes in mechanical loading, process the signal, and develop context-specific adaptive responses to rebalance the cell homeostatic state. The significance of the interactions between specific mechanical forces in the EC microenvironment together with circulating bioactive molecules in the progression and resolution of vascular pathologies including vascular injury, atherosclerosis, pulmonary edema, and acute respiratory distress syndrome has been only recently recognized. This review will summarize the current understanding of EC mechanosensory mechanisms, modulation of EC responses to humoral factors by surrounding mechanical forces (particularly the cyclic stretch), and discuss recent findings of magnitude-specific regulation of EC functions by transcriptional, posttranscriptional and epigenetic mechanisms using -omics approaches. We also discuss ongoing challenges and future opportunities in developing new therapies targeting dysregulated mechanosensing mechanisms to treat vascular diseases. (C) 2019 American Physiological Society.
引用
收藏
页码:873 / 904
页数:32
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