Rapid flow-induced responses in endothelial cells

被引:28
作者
Stamatas, GN [1 ]
McIntire, LV [1 ]
机构
[1] Rice Univ, Inst Biosci & Bioengn, Cox Lab Biomed Engn, Houston, TX 77251 USA
关键词
D O I
10.1021/bp0100272
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Endothelial cells alter their morphology, growth rate, and metabolism in response to fluid shear stress. To study rapid flow-induced responses in the 3D endothelial cell morphology and calcium distribution, coupled fluorescence microscopy with optical sectioning, digital imaging, and numerical deconvolution techniques have been utilized. Results demonstrate that within the first minutes of flow application nuclear calcium is increasing. In the same time frame whole cell height and nuclear height are reduced by about 1 mum. Whole cell height changes may facilitate reduction of shear stress gradients on the luminal surface, whereas nuclear structural changes may be important for modulating endothelial growth rate and metabolism. To study the role of the cytoskeleton in these responses, endothelial cells have been treated with specific disrupters (acrylamide, cytochalasin D, and colchicine) of each of the cytoskeleton elements (intermediate filaments, microfilaments, and microtubules, respectively). None of these compounds had any effect on the shear-induced calcium response. Cytochalasin D and acrylamide did not affect the shear-induced nuclear morphology changes. Colchicine, however, completely abrogated the response, indicating that microtubules may be implicated in force transmission from the plasma membrane to the nucleus. A pedagogical model based on tensegrity theory principles is presented that is consistent with the results on the 3D endothelial morphology.
引用
收藏
页码:383 / 402
页数:20
相关论文
共 100 条
[1]  
AGARD DA, 1989, SPIE, V1161, P24
[2]  
ANDO J, 1988, IN VITRO CELL DEV B, V24, P871
[3]   SHEAR STRESS-INDUCED REORGANIZATION OF THE SURFACE-TOPOGRAPHY OF LIVING ENDOTHELIAL-CELLS IMAGED BY ATOMIC-FORCE MICROSCOPY [J].
BARBEE, KA ;
DAVIES, PF ;
LAL, R .
CIRCULATION RESEARCH, 1994, 74 (01) :163-171
[4]  
Bershadsky AD., 1988, CYTOSKELETON, V1st
[5]  
BERTHIAUME F, 1993, PHYSICAL FORCES MAMM
[6]   MECHANISM OF SHEAR-INDUCED PROSTACYCLIN PRODUCTION IN ENDOTHELIAL-CELLS [J].
BHAGYALAKSHMI, A ;
FRANGOS, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 158 (01) :31-37
[7]   COLCHICINE INDUCES APOPTOSIS IN CEREBELLAR GRANULE CELLS [J].
BONFOCO, E ;
CECCATELLI, S ;
MANZO, L ;
NICOTERA, P .
EXPERIMENTAL CELL RESEARCH, 1995, 218 (01) :189-200
[8]  
BOTTERI FM, 1990, J BIOL CHEM, V265, P13327
[9]   CONFOCAL MICROSCOPY TO ANALYZE CYTOSOLIC AND NUCLEAR CALCIUM IN CULTURED VASCULAR CELLS [J].
BURNIER, M ;
CENTENO, G ;
BURKI, E ;
BRUNNER, HR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (04) :C1118-C1127
[10]   ESTIMATING SOLUTIONS OF 1ST KIND INTEGRAL-EQUATIONS WITH NONNEGATIVE CONSTRAINTS AND OPTIMAL SMOOTHING [J].
BUTLER, JP ;
REEDS, JA ;
DAWSON, SV .
SIAM JOURNAL ON NUMERICAL ANALYSIS, 1981, 18 (03) :381-397