Proliferation and differentiation of rat calvarial osteoblasts on type I collagen-coated titanium alloy

被引:103
作者
Becker, D
Geissler, U
Hempel, U
Bierbaum, S
Scharnweber, D
Worch, H
Wenzel, KW
机构
[1] Dresden Univ Technol, Med Fac Carl Gustav Carus, Inst Physiol Chem, D-01307 Dresden, Germany
[2] Dresden Univ Technol, Inst Sci Mat, Dresden, Germany
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 2002年 / 59卷 / 03期
关键词
osteoblast; collagen type I coating; titanium alloy; differentiation; mineralization;
D O I
10.1002/jbm.1265
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Several attempts have been made to improve osseointegration of titanium alloy as an implant material by modification of its surface. In the present study, proliferation, differentiation, and mineralization of osteoblasts on type I collagen-coated Ti6Al4V were investigated. The activity of alkaline phosphatase and the accumulation of calcium by osteoblasts grown on titanium alloy were significantly higher compared to cells grown on polystyrene. Precoating of the implant surface with type I collagen did not extensively affect proliferation, the activity of alkaline phosphatase, collagen synthesis, calcium accumulation, or the mRNA levels for collagen I alpha1, osteopontin, osteocalcin, MMP-2, and TIMP-2. Maximum collagen synthesis by osteoblasts was observed at day 4 of culture independent of the type of implant material. The specific activity of alkaline phosphatase reached its maximum at day 18 of culture. Accumulation of calcium and elevated mRNA levels for osteocalcin were found at day 22. These results indicate that collagen-coating alone is not sufficient to accelerate differentiation of rat calvarial osteoblasts on Ti6Al4V. (C) 2001 John Wiley & Sons, Inc. J Biomed Mater Res 59: 516-527, 2002.
引用
收藏
页码:516 / 527
页数:12
相关论文
共 45 条
[1]   GROWTH ON TYPE-I COLLAGEN PROMOTES EXPRESSION OF THE OSTEOBLASTIC PHENOTYPE IN HUMAN OSTEOSARCOMA MG-63 CELLS [J].
ANDRIANARIVO, AG ;
ROBINSON, JA ;
MANN, KG ;
TRACY, RP .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 153 (02) :256-265
[2]  
AZZAM HS, 1992, CANCER RES, V52, P4540
[3]   Type I collagen influence on gene expression in UMR106-06 osteoblast-like cells is inhibited by genistein [J].
Celic, S ;
Katayama, Y ;
Chilco, PJ ;
Martin, TJ ;
Findlay, DM .
JOURNAL OF ENDOCRINOLOGY, 1998, 158 (03) :377-388
[4]   EXPRESSION OF COLLAGEN, OSTEOCALCIN, AND BONE ALKALINE-PHOSPHATASE IN A MINERALIZING RAT OSTEOBLASTIC CELL-CULTURE [J].
COLLIN, P ;
NEFUSSI, JR ;
WETTERWALD, A ;
NICOLAS, V ;
BOYLEFEVRE, ML ;
FLEISCH, H ;
FOREST, N .
CALCIFIED TISSUE INTERNATIONAL, 1992, 50 (02) :175-183
[5]  
Cooper L F, 1993, Int J Oral Maxillofac Implants, V8, P264
[6]   Biologic determinants of bone formation for osseointegration: Clues for future clinical improvements [J].
Cooper, LF .
JOURNAL OF PROSTHETIC DENTISTRY, 1998, 80 (04) :439-449
[7]   Gelatinase A (MMP-2) and cysteine proteinases are essential for the degradation of collagen in soft connective tissue [J].
Creemers, LB ;
Jansen, IDC ;
Docherty, AJP ;
Reynolds, JJ ;
Beertsen, W ;
Everts, V .
MATRIX BIOLOGY, 1998, 17 (01) :35-46
[9]   Conditions which promote mineralization at the bone-implant interface: A model in vitro study [J].
Dee, KC ;
Rueger, DC ;
Andersen, TT ;
Bizios, R .
BIOMATERIALS, 1996, 17 (02) :209-215
[10]   Effects of roughness, fibronectin and vitronectin on attachment, spreading, and proliferation of human osteoblast-like cells (Saos-2) on titanium surfaces [J].
Degasne, I ;
Baslé, MF ;
Demais, V ;
Huré, G ;
Lesourd, M ;
Grolleau, B ;
Mercier, L ;
Chappard, D .
CALCIFIED TISSUE INTERNATIONAL, 1999, 64 (06) :499-507