Bacterial cellulose as a potential scaffold for tissue engineering of cartilage

被引:777
作者
Svensson, A
Nicklasson, E
Harrah, T
Panilaitis, B
Kaplan, DL
Brittberg, M
Gatenholm, P [1 ]
机构
[1] Chalmers Univ Technol, Dept Mat & Surface Chem Biopolymer Technol, SE-41296 Gothenburg, Sweden
[2] Tufts Univ, Dept Biol & Chem Engn, Medford, MA 02155 USA
[3] Univ Gothenburg, Kungsbacka Hosp, Cartilage Res Unit, Dept Orthopaed, SE-43480 Kungsbacka, Sweden
关键词
cellulose; cartilage tissue engineering; chondrocytes; scaffold;
D O I
10.1016/j.biomaterials.2004.02.049
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tissue constructs for cartilage with native mechanical properties have not been described to date. To address this need the bacterial cellulose (BC) secreted by Gluconacetobacter xylinus ( = Acetobacter xylinum) was explored as a novel scaffold material due to its unusual material properties and degradability. Native and chemically modified BC materials were evaluated using bovine chondrocytes. The results indicate that unmodified BC supports chondrocyte proliferation at levels of approximately 50% of the collagen type II substrate while providing significant advantages in terms of mechanical properties. Compared to tissue culture plastic and calcium alginate, unmodified BC showed significantly higher levels of chondrocyte growth. Chemical sulfation and phosphorylation of the BC, performed to mimic the glucosaminoglycans of native cartilage, did not enhance chondrocyte growth while the porosity of the material did affect chondrocyte viability. The BC did not induce significant activation of proinflammatory cytokine production during in vitro macrophage screening. Hence, unmodified BC was further explored using human chondrocytes. TEM analysis and RNA expression of the collagen II from human chondrocytes indicated that unmodified BC supports proliferation of chondrocytes. In addition, ingrowth of chondrocytes into the scaffold was verified by TEM. The results suggest the potential for this biomaterial as a scaffold for tissue engineering of cartilage. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:419 / 431
页数:13
相关论文
共 39 条
[1]  
Brun P, 1999, J BIOMED MATER RES, V46, P337, DOI 10.1002/(SICI)1097-4636(19990905)46:3<337::AID-JBM5>3.0.CO
[2]  
2-Q
[3]   Hydrogel properties influence ECM production by chondrocytes photoencapsulated in poly(ethylene glycol) hydrogels [J].
Bryant, SJ ;
Anseth, KS .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 59 (01) :63-72
[4]   CHONDROCYTES IN AGAROSE CULTURE SYNTHESIZE A MECHANICALLY FUNCTIONAL EXTRACELLULAR-MATRIX [J].
BUSCHMANN, MD ;
GLUZBAND, YA ;
GRODZINSKY, AJ ;
KIMURA, JH ;
HUNZIKER, EB .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1992, 10 (06) :745-758
[5]   Polymer/alginate amalgam for cartilage-tissue engineering [J].
Caterson, EJ ;
Li, WJ ;
Nesti, LJ ;
Albert, T ;
Danielson, K ;
Tuan, RS .
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS, 2002, 961 :134-138
[6]   Biological response of chondrocytes to hydrogels [J].
Elisseeff, JH ;
Lee, A ;
Kleinman, HK ;
Yamada, Y .
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS, 2002, 961 :118-122
[7]   Tissue engineering of cartilage in space [J].
Freed, LE ;
Langer, R ;
Martin, I ;
Pellis, NR ;
VunjakNovakovic, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) :13885-13890
[8]  
FREEMAN MAR, 1973, ADULT ARTICULAR CART
[9]  
Grande DA, 1997, J BIOMED MATER RES, V34, P211, DOI 10.1002/(SICI)1097-4636(199702)34:2<211::AID-JBM10>3.0.CO
[10]  
2-L