IMAGING OF CELL/SUBSTRATE CONTACTS ON POLYMERS BY TOTAL INTERNAL-REFLECTION FLUORESCENCE MICROSCOPY

被引:4
作者
BURMEISTER, JS
TRUSKEY, GA
YARBROUGH, JL
REICHERT, WM
机构
[1] DUKE UNIV, DEPT BIOMED ENGN, DURHAM, NC 27706 USA
[2] DUKE UNIV, CTR BIOCHEM ENGN, DURHAM, NC 27706 USA
关键词
D O I
10.1021/bp00025a003
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
A simplified model of total internal reflection fluorescence (TIRF) emission of fluorescently labeled cell membranes [Reichert, W. M.; Truskey, G. A. J. Cell Sci. 1990, 96, 219-230] was used to determine the topography of the cell membrane in apposition to a polymer-coated surface, The homopolymer substrates were spun cast films of hydrophilic poly(hydroxyethyl methacrylate) (polyHEMA) or hydrophobic poly(ethyl methacrylate) (polyEMA). Bovine aortic endothelial cells (BAEC) on preadsorbed fibronectin polymer substrates were either plated for 24 h, fixed, labeled, and examined by TIRF microscopy (TIRFM) and phase-contrast microscopy or plated for 2 h and tested for their adhesion strength in a parallel-plate flow chamber. BAEC attached to polyHEMA showed nb evidence of focal contact formation. However, BAEC attached to polyEMA were well spread and showed an array of focal contacts. TIRFM data were transformed to construct a detailed topographical map of relative cell/substrate separation distances. Virtually all of the BAEC plated to polyHEMA were sheared from the surface when subjected to a 50 dyn/cm(2) burst of laminar flow, whereas only 10 % of the BAEC were sheared from the polyEMA surface. These data suggest that the polyHEMA and polyEMA Surface properties (e.g., hydrophobicity) correlate with,the presence of BAEC focal contacts and the BAEC attachment strength.
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页码:26 / 31
页数:6
相关论文
共 26 条
[1]  
ANDRADE JD, 1976, ACS S SER, V31
[2]  
AXELROD D, 1990, NONINVASIVE TECHNIQU, P93
[3]  
BIRD RB, 1960, TRANSPORT PHENOMENA, P47
[4]  
BURMEISTER JS, 1994, IN PRESS J MICROSC
[5]   FOCAL ADHESIONS - TRANSMEMBRANE JUNCTIONS BETWEEN THE EXTRACELLULAR-MATRIX AND THE CYTOSKELETON [J].
BURRIDGE, K ;
FATH, K ;
KELLY, T ;
NUCKOLLS, G ;
TURNER, C .
ANNUAL REVIEW OF CELL BIOLOGY, 1988, 4 :487-525
[6]   IMMUNOELECTRON MICROSCOPIC STUDIES OF THE SITES OF CELL-SUBSTRATUM AND CELL-CELL CONTACTS IN CULTURED FIBROBLASTS [J].
CHEN, WT ;
SINGER, SJ .
JOURNAL OF CELL BIOLOGY, 1982, 95 (01) :205-222
[7]   ENDOTHELIAL-CELL ADHESION IN REAL-TIME - MEASUREMENTS INVITRO BY TANDEM SCANNING CONFOCAL IMAGE-ANALYSIS [J].
DAVIES, PF ;
ROBOTEWSKYJ, A ;
GRIEM, ML .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2640-2652
[8]   THE REACTION-LIMITED KINETICS OF MEMBRANE-TO-SURFACE ADHESION AND DETACHMENT [J].
DEMBO, M ;
TORNEY, DC ;
SAXMAN, K ;
HAMMER, D .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1988, 234 (1274) :55-83
[9]   FOCAL ADHESION SITES AND THE REMOVAL OF SUBSTRATUM-BOUND FIBRONECTIN [J].
GRINNELL, F .
JOURNAL OF CELL BIOLOGY, 1986, 103 (06) :2697-2706
[10]  
Grinnell F, 1978, Int Rev Cytol, V53, P65