Engineering structurally organized cartilage and bone tissues

被引:247
作者
Sharma, B [1 ]
Elisseeff, JH [1 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
关键词
cartilage tissue engineering; musculoskeletal tissues; scaffolds; photopolymerizinig hydrogels;
D O I
10.1023/B:ABME.0000007799.60142.78
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The field of tissue engineering promises to deliver biological substitutes to repair or replace tissues in the body that have been injured or diseased. The clinical demand for musculoskeletal tissues is particularly high, especially for cartilage and bone defects. Although they are generally considered biologically simple structures, musculoskeletal tissues consist of highly organized three-dimensional networks of cells and matrix, giving rise to tissue structures with remarkable mechanical properties. Although the field of cartilage and bone tissue engineering has progressed significantly in recent years, the development of structurally ordered tissues has not been accomplished. More strategies are needed to ensure that the appropriate cell and matrix organization is being achieved in the engineered tissues. This review emphasizes how different cell types and scaffold designs can be used to modulate tissue properties and engineer more complex tissue structures, with emphasis on cartilage and bone tissues.
引用
收藏
页码:148 / 159
页数:12
相关论文
共 109 条
[1]  
Agrawal CM, 2001, J BIOMED MATER RES, V55, P141, DOI 10.1002/1097-4636(200105)55:2<141::AID-JBM1000>3.0.CO
[2]  
2-J
[3]   Engineering growing tissues [J].
Alsberg, E ;
Anderson, KW ;
Albeiruti, A ;
Rowley, JA ;
Mooney, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (19) :12025-12030
[4]   Cell differentiation by mechanical stress [J].
Altman, GH ;
Horan, RL ;
Martin, I ;
Farhadi, J ;
Stark, PRH ;
Volloch, V ;
Richmond, JC ;
Vunjak-Novakovic, G ;
Kaplan, DL .
FASEB JOURNAL, 2001, 15 (14) :270-+
[5]   In situ forming degradable networks and their application in tissue engineering and drug delivery [J].
Anseth, KS ;
Metters, AT ;
Bryant, SJ ;
Martens, PJ ;
Elisseeff, JH ;
Bowman, CN .
JOURNAL OF CONTROLLED RELEASE, 2002, 78 (1-3) :199-209
[6]  
ARCHER CW, 1990, J CELL SCI, V97, P361
[7]   Insulin production by human embryonic stem cells [J].
Assady, S ;
Maor, G ;
Amit, M ;
Itskovitz-Eldor, J ;
Skorecki, KL ;
Tzukerman, M .
DIABETES, 2001, 50 (08) :1691-1697
[8]   DIFFERENCES BETWEEN SUB-POPULATIONS OF CULTURED BOVINE ARTICULAR CHONDROCYTES .2. PROTEOGLYCAN METABOLISM [J].
AYDELOTTE, MB ;
GREENHILL, RR ;
KUETTNER, KE .
CONNECTIVE TISSUE RESEARCH, 1988, 18 (03) :223-234
[9]   DIFFERENCES BETWEEN SUB-POPULATIONS OF CULTURED BOVINE ARTICULAR CHONDROCYTES .1. MORPHOLOGY AND CARTILAGE MATRIX PRODUCTION [J].
AYDELOTTE, MB ;
KUETTNER, KE .
CONNECTIVE TISSUE RESEARCH, 1988, 18 (03) :205-222
[10]   DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224