Effects of flow patterns on the localization and expression of VE-cadherin at vascular endothelial cell junctions: In vivo and in vitro investigations

被引:126
作者
Miao, H
Hu, YL
Shiu, YT
Yuan, SL
Zhao, YH
Kaunas, R
Wang, YX
Jin, G
Usami, S
Chien, S
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Whitaker Inst Biomed Engn, La Jolla, CA 92093 USA
关键词
endothelial cell; flow; in vivo; stenosis; VE-cadherin;
D O I
10.1159/000083094
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Atherosclerosis occurs preferentially at vascular curvature and branch sites where the vessel walls are exposed to fluctuating shear stress and have high endothelial permeability. Endothelial permeability is modulated by intercellular adhesion molecules such as VE- cadherin. This study was designed to elucidate the effects of different flow patterns on the localization and expression of VE-cadherin in endothelial cells ( ECs) both in vivo and in vitro. VE- cadherin staining at EC borders was much stronger in the descending thoracic aorta and abdominal aorta, where the pulsatile flow has a strong net forward component than in the aortic arch and the poststenotic dilatation site beyond an experimental constriction, where the flow near the wall is complex and reciprocating with little net flow. With the use of flow chambers the effects of pulsatile flow ( 12 +/- 4 dyn/ cm(2) at 1 Hz) and reciprocating flow ( 0.5 +/- 4 dyn/ cm(2) at 1 Hz) on VE- cadherin organization in endothelial monolayers were studied in vitro. VE- cadherin staining was continuous along cell borders in static controls. Following 6 h of either pulsatile or reciprocating flow, the VE- cadherin staining at cell borders became intermittent. When the pulsatile flow was extended to 24, 48 or 72 h the staining around the cell borders became continuous again, but the staining was still intermittent when the reciprocating flow was similarly extended. Exposure to pulsatile or reciprocating flow for 6 and 24 h neither change the expression level of VE- cadherin nor its distribution between membrane and cytosol fractions as determined by Western blot and compared with static controls. These findings suggest that the cell junction remodeling induced by different flow patterns may result from a redistribution of VE- cadherin within the cell membrane. Both the in vivo and in vitro data indicate that pulsatile and reciprocating flow patterns have different effects on cell junction remodeling. The lack of junction reorganization in regions of reciprocating flow in vivo and in vitro may provide a mechanistic basis for the high permeability and the preferential localization of atherosclerosis in regions of the arterial stress with complex flow patterns and fluctuating shear stress. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:77 / 89
页数:13
相关论文
共 62 条
[1]   VELOCITY-MEASUREMENTS IN STEADY FLOW THROUGH AXISYMMETRIC STENOSES AT MODERATE REYNOLDS-NUMBERS [J].
AHMED, SA ;
GIDDENS, DP .
JOURNAL OF BIOMECHANICS, 1983, 16 (07) :505-&
[2]   ATP-independent membrane depolarization with ischemia in the oxygen-ventilated isolated rat lung [J].
Al-Mehdi, AB ;
Zhao, GC ;
Fisher, AB .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 18 (05) :653-661
[3]   The role of cadherin endocytosis in endothelial barrier regulation: Involvement of protein kinase C and actin-cadherin interactions [J].
Alexander, JS ;
Jackson, SA ;
Chaney, E ;
Kevil, CG ;
Haselton, FR .
INFLAMMATION, 1998, 22 (04) :419-433
[4]   Microcinematographic studies of flow patterns in the excised rabbit aorta and its major branches [J].
Barakat, AI ;
Karino, T ;
Colton, CK .
BIORHEOLOGY, 1997, 34 (03) :195-221
[5]   TOPOGRAPHICAL MAPPING OF SITES OF ENHANCED HRP PERMEABILITY IN THE NORMAL RABBIT AORTA [J].
BARAKAT, AI ;
UHTHOFF, PAF ;
COLTON, CK .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1992, 114 (03) :283-292
[6]   PATTERNS OF AORTIC EVANS BLUE UPTAKE IN-VIVO AND IN-VITRO [J].
BELL, FP ;
SOMER, JB ;
CRAIG, IH ;
SCHWARTZ, CJ .
ATHEROSCLEROSIS, 1972, 16 (03) :369-375
[7]   ATHEROMA AND ARTERIAL WALL SHEAR - OBSERVATION, CORRELATION AND PROPOSAL OF A SHEAR DEPENDENT MASS TRANSFER MECHANISM FOR ALTHEROGENESIS [J].
CARO, CG ;
FITZGERA.JM ;
SCHROTER, RC .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1971, 177 (1046) :109-+
[8]   ULTRASTRUCTURAL STUDIES ON MACROMOLECULAR PERMEABILITY IN RELATION TO ENDOTHELIAL-CELL TURNOVER [J].
CHEN, YL ;
JAN, KM ;
LIN, HS ;
CHIEN, S .
ATHEROSCLEROSIS, 1995, 118 (01) :89-104
[9]  
Chien S, 2003, PROG BIOPHYS MOL BIO, V83, P131, DOI [10.1016/S0079-6107(03)00053-1, 10.1016/s0079-6107(03)00053-1]
[10]   Effects of disturbed flow on endothelial cells [J].
Chiu, JJ ;
Wang, DL ;
Chien, S ;
Skalak, R ;
Usami, S .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1998, 120 (01) :2-8