Collagen-based biomaterials as 3D scaffold for cell cultures: applications for tissue engineering and gene therapy

被引:270
作者
Chevallay, B [1 ]
Herbage, D [1 ]
机构
[1] CNRS, Inst Biol & Chim Prot, UPR 412, Lyon, France
关键词
biomaterials; collagen; tissue engineering; gene therapy;
D O I
10.1007/BF02344779
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Many substances are used in the production of biomaterials: metals (titanium), ceramics (alumina), synthetic polymers (polyurethanes, silicones, polyglycolic acid (PGA), polylactic acid (PLA), copolymers of lactic and glycolic acids (PLGA), polyanhydrides, polyorthoesters) and natural polymers (chitosan, glycosaminoglycans, collagen). With the rapid development in tissue engineering, these different biomaterials have been used as three-dimensional scaffolds and cell transplant devices. The principal biochemical and biological characteristics of the collagen-based biomaterials are presented, including their interactions with cells (fibroblasts), distinct from those of synthetic polymers, and their potential use in gene therapy through the formation of neo-organs or organoids.
引用
收藏
页码:211 / 218
页数:8
相关论文
共 87 条
[51]  
MIYATA T, 1992, Clinical Materials, V9, P139, DOI 10.1016/0267-6605(92)90093-9
[53]   CONTINUOUS SYSTEMIC SECRETION OF A LYSOSOMAL-ENZYME BY GENETICALLY-MODIFIED MOUSE SKIN FIBROBLASTS [J].
MOULLIER, P ;
MARECHAL, V ;
DANOS, O ;
HEARD, JM .
TRANSPLANTATION, 1993, 56 (02) :427-432
[54]   SUSTAINED DELIVERY OF ERYTHROPOIETIN IN MICE BY GENETICALLY-MODIFIED SKIN FIBROBLASTS [J].
NAFFAKH, N ;
HENRI, A ;
VILLEVAL, JL ;
ROUYERFESSARD, P ;
MOULLIER, P ;
BLUMENFELD, N ;
DANOS, O ;
VAINCHENKER, W ;
HEARD, JM ;
BEUZARD, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3194-3198
[55]   LONG-TERM CULTURE OF FIBROBLASTS IN CONTRACTED COLLAGEN GELS - EFFECTS ON CELL-GROWTH AND BIOSYNTHETIC ACTIVITY [J].
NAKAGAWA, S ;
PAWELEK, P ;
GRINNELL, F .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 93 (06) :792-798
[56]   EXTRACELLULAR-MATRIX ORGANIZATION MODULATES FIBROBLAST GROWTH AND GROWTH-FACTOR RESPONSIVENESS [J].
NAKAGAWA, S ;
PAWELEK, P ;
GRINNELL, F .
EXPERIMENTAL CELL RESEARCH, 1989, 182 (02) :572-582
[57]   Polypeptide growth factors: targeted delivery systems [J].
Nimni, ME .
BIOMATERIALS, 1997, 18 (18) :1201-1225
[58]   GROWTH-RATE OF HUMAN-FIBROBLASTS IS REPRESSED BY THE CULTURE WITHIN RECONSTITUTED COLLAGEN MATRIX BUT NOT BY THE CULTURE ON THE MATRIX [J].
NISHIYAMA, T ;
TSUNENAGA, M ;
NAKAYAMA, Y ;
ADACHI, E ;
HAYASHI, T .
MATRIX, 1989, 9 (03) :193-199
[59]  
NUSGENS B, 1984, COLLAGEN REL RES, V4, P351
[60]  
OBRIEN TK, 1984, T AM SOC ART INT ORG, V30, P440