Regulation of bovine brain microvascular endothelial tight junction assembly and barrier function by laminar shear stress

被引:99
|
作者
Colgan, Olga C.
Ferguson, Gail
Collins, Nora T.
Murphy, Ronan P.
Meade, Gerardeane
Cahill, Paul A.
Cummins, Philip M. [1 ]
机构
[1] Dublin City Univ, Vasc Hlth Res Ctr, Dublin 9, Ireland
[2] Royal Coll Surgeons Ireland, Dept Mol & Cellular Therapeut, Dublin 2, Ireland
基金
英国惠康基金;
关键词
blood-brain barrier; occludin; zonula occludens-1;
D O I
10.1152/ajpheart.01177.2006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Blood-brain barrier (BBB) controls paracellular solute diffusion into the brain microenvironment and is maintained primarily by tight junctions between adjacent microvascular endothelial cells. Studies implicate blood flow-associated shear stress as a pathophysiological mediator of BBB function, although detailed biochemical data are scarce. We hypothesize that shear stress upregulates BBB function via direct modulation of expression and properties of pivotal tight-junction proteins occludin and zonula occludens-1 (ZO-1). Bovine brain microvascular endothelial cells (BBMvECs) were exposed to either steady or Pulsatile shear stress (10 and 14 dyn/cm(2) 2, respectively) for 24 h. Sheared BBMvECs were monitored for occludin-ZO-1 expression, association, and subcellular localization, and transendothelial permeability of BBMvECs to FITC-dextran and (14)[C]sucrose was assessed. Actin reorganization and BBMvEC realignment were observed following steady shear stress for 24 h. Substantial increases in occludin rnRNA and protein expression (2.73 +/- 0.26- and 1.83 +/- 0.03-fold) and in occludin-ZO-1 association (2.12 +/- 0.15-fold) were also observed. Steady shear stress also induced clear relocalization of both proteins to the cell-cell border in parallel with reduced transendothelial permeability to FITC-dextran (but not Sucrose). Following pulsatile shear stress, increased protein levels for both occludin and ZO-1 (2.15 +/- 0.02- and 1.67 +/- 0.21-fold) and increased occludin-ZO-1 association (2.91 +/- 0.14-fold) were observed in parallel with a reduction in transendothelial permeability to (14)[C]sucrose. Shear stress upregulates BBMvEC barrier function at the molecular level via modulation of expression, association, and localization of occludin and ZO-1. The pulsatile shear model appeared to give the most profound biochemical responses.
引用
收藏
页码:H3190 / H3197
页数:8
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