Synergistic effect of titanium alloy and collagen type I on cell adhesion, proliferation and differentiation of osteoblast-like cells

被引:92
作者
Roehlecke, C
Witt, M
Kasper, M
Schulze, E
Wolf, C
Hofer, A
Funk, RHW
机构
[1] Tech Univ Dresden, Dept Anat, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Dept Mat Sci, D-01307 Dresden, Germany
[3] Tech Univ Dresden, Clin Reconstruct Surg, D-01307 Dresden, Germany
关键词
titanium; osteoblasts; collagen type I; focal adhesions; immunocytochemistry; rat;
D O I
10.1159/000047833
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
A number of studies have demonstrated the pivotal role of collagen in modulating cell growth and differentiation. In bone, where the extracellular matrix is composed of approximately 85% type I collagen, cellular interaction with matrix components has been shown to be important in the regulation of the osteoblast phenotype. Preservation or enhancement of normal osteoblast function and appositional bone formation after implant placement represents a strategy that can be useful I for the purpose of improving osseointegration. In order to further improve biocompatibility, we combined two known favorable compounds, namely the titanium alloy, Ti6A14V, with type I collagen. We assessed the in vitro behavior of primary osteoblasts grown on both fibrillar collagen-coated and tropocollagen-coated Ti6A14V in comparison with uncoated titanium alloy, using an improved adsorption procedure. As parameters of biocompatibility, a variety of processes, including cell attachment, spreading, cytoskeletal organization, focal contact formation, proliferation and expression of a differentiated phenotype, were investigated. Our results demonstrated for the first time that in comparison to uncoated titanium alloy, collagen-coated alloy enhanced spreading and resulted in a more rapid formation of focal adhesions and their associated stress fibers. Growing on collagen-coated Ti6A14V, osteoblasts had a higher proliferative capacity and the intracellular expression of osteopontin was upregulated compared to uncoated titanium alloy. Type I collagen-coated titanium alloy exhibits favorable effects on the initial adhesion and growth activities of osteoblasts, which is encouraging for its potential use as bone graft material. Moreover, collagen type I may serve as an excellent biocompatible carrier for osteotropic factors such as cell adhesion molecules (e.g. fibronectin) or bone-specific growth factors. Copyright (C) 2001 S.Karger AG, Basel.
引用
收藏
页码:178 / 187
页数:10
相关论文
共 59 条
[1]   INTEGRINS AND OTHER CELL-ADHESION MOLECULES [J].
ALBELDA, SM ;
BUCK, CA .
FASEB JOURNAL, 1990, 4 (11) :2868-2880
[2]   OSSEOINTEGRATION OF BONE IMPLANTS - A REVIEW OF AN ALTERNATIVE MODE OF FIXATION [J].
ALBREKTSSON, T ;
ALBREKTSSON, B .
ACTA ORTHOPAEDICA SCANDINAVICA, 1987, 58 (05) :567-577
[3]   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
[4]   FACTORS THAT PROMOTE PROGRESSIVE DEVELOPMENT OF THE OSTEOBLAST PHENOTYPE IN CULTURED FETAL-RAT CALVARIA CELLS [J].
ARONOW, MA ;
GERSTENFELD, LC ;
OWEN, TA ;
TASSINARI, MS ;
STEIN, GS ;
LIAN, JB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (02) :213-221
[5]   MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM ;
ANTOSZ, ME .
CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) :143-154
[6]   PHENOTYPIC DIFFERENCES IN SUBCLONES AND LONG-TERM CULTURES OF CLONALLY DERIVED RAT BONE CELL-LINES [J].
BELLOWS, CG ;
SODEK, J ;
YAO, KL ;
AUBIN, JE .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1986, 31 (02) :153-169
[7]  
BURRIDGE K, 1988, ANNU REV CELL BIOL, V4, P487, DOI 10.1146/annurev.cb.04.110188.002415
[8]   BIOIMPLANT SURFACES - BINDING OF FIBRONECTIN AND FIBROBLAST ADHESION [J].
CANNAS, M ;
DENICOLAI, F ;
WEBB, LX ;
GRISTINA, AG .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1988, 6 (01) :58-62
[9]  
Carvalho RS, 1998, J CELL BIOCHEM, V70, P376, DOI 10.1002/(SICI)1097-4644(19980901)70:3<376::AID-JCB11>3.0.CO
[10]  
2-J