The effect of surface roughness on fibroblast adhesion in vitro

被引:0
作者
Richards, RG
机构
来源
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED | 1996年 / 27卷
关键词
scanning electron microscopy; back-scattered electron imaging; cells; adhesion; infection; image analysis;
D O I
暂无
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Adhesion of tissue cells to biomaterial implants is a major factor of their biocompatibility. Quantitative or qualitative adhesion measurements would therefore be useful in the screening of new implant materials. Results from a quantitative method of measuring the total cell adhesion area of cultured cells is presented. It is postulated that the more compatible the surface, the greater the amount of cell adhesion. Fibroblastic cells were cultured on discs of plastic (Thermanox), commercially pure titanium (LSO 5832/2) or steel (ISO 5832/1), as used in AO fixation plates. The cells were fixed, stained, embedded in resin and their discs removed. Backscattered electron (BSE) imaging in a scanning electron microscope displayed the stained cells within the unstained resin. Imaging at high beam energy allowed visualization of the entire cell. Low beam energy displayed the regions of cell contact with the substrate, i.e. the focal adhesion sites. Images were analyzed with an image analysis and measurement system which allowed the percentage of the cell area involved with adhesion to be calculated. Results show that the material roughness, with the materials and cells tested, does not affect the total amount of cell adhesion. Implant surface design to encourage cell adhesion and discourage bacterial adhesion is discussed.
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页码:38 / 43
页数:6
相关论文
共 13 条
[1]  
BOXMA H, 1995, THESIS U AMSTERDAM
[2]   THE ADHESIVENESS OF NORMAL AND SV40-TRANSFORMED BALB/C 3T3-CELLS - EFFECTS OF CULTURE DENSITY AND SHEAR RATE [J].
ELVIN, P ;
EVANS, CW .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1982, 18 (07) :669-675
[3]  
ELVIN P, 1983, BIOL CELL, V48, P1
[4]   DETACHMENT OF AGGLUTININ-BONDED RED-BLOOD-CELLS .1. FORCES TO RUPTURE MOLECULAR-POINT ATTACHMENTS [J].
EVANS, E ;
BERK, D ;
LEUNG, A .
BIOPHYSICAL JOURNAL, 1991, 59 (04) :838-848
[5]  
KONONEN M, 1992, J BIOMED MATER RES, V26, P1325
[6]   CELL-ADHESION TO FIBRONECTIN AND TENASCIN - QUANTITATIVE MEASUREMENTS OF INITIAL BINDING AND SUBSEQUENT STRENGTHENING RESPONSE [J].
LOTZ, MM ;
BURDSAL, CA ;
ERICKSON, HP ;
MCCLAY, DR .
JOURNAL OF CELL BIOLOGY, 1989, 109 (04) :1795-1805
[7]   CHANGES IN SURFACE MORPHOLOGY OF CHINESE-HAMSTER OVARY CELLS DURING CELL CYCLE [J].
PORTER, K ;
PRESCOTT, D ;
FRYE, J .
JOURNAL OF CELL BIOLOGY, 1973, 57 (03) :815-836
[8]  
REID G, 1989, COLLOID SURFACE, V42, P299, DOI 10.1016/0166-6622(89)80347-6
[9]   BACKSCATTERED ELECTRON IMAGING OF THE UNDERSURFACE OF RESIN-EMBEDDED CELLS BY FIELD-EMISSION SCANNING ELECTRON-MICROSCOPY [J].
RICHARDS, RG ;
APGWYNN, I .
JOURNAL OF MICROSCOPY-OXFORD, 1995, 177 :43-52
[10]   SCANNING ELECTRON-MICROSCOPY OF THE UNDERSURFACE OF CELL MONOLAYERS GROWN ON METALLIC IMPLANTS [J].
RICHARDS, RG ;
RAHN, BA ;
GWYNN, IAP .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1995, 6 (02) :120-124