Gene delivery strategies for cartilage tissue engineering

被引:114
作者
Saraf, Anita [1 ]
Mikos, Antonios G. [1 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
关键词
cartilage tissue engineering; genes; gene delivery; gene therapy; gene delivery vectors; MSCs; chondrocytes; synovial cells;
D O I
10.1016/j.addr.2006.03.005
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Tissue engineering is a multifaceted technology developed with a purpose of regenerating complex tissues and organs. Cartilage regeneration continues to challenge engineers and a new wave of efforts focus on developing strategies that provide sustained stimulation to cells by growth factors and other biological molecules to promote their differentiation into chondrocytes. Though significant research is dedicated to developing controlled release systems that deliver growth factors directly, a simpler approach to resolving this dilemma involves converting cells into protein producing factories. This is done through gene delivery. Gene Therapy studies published for articular diseases such as rheumatoid and osteoarthritis provide valuable information regarding different types of cells, gene delivery vectors and genes that can potentially be used to regenerate cartilage. Tissue engineering approaches provide the opportunity to combine two or more strategies used for Gene Therapy thus far and create a cohesive system that addresses both cartilage degeneration and synthesis simultaneously. Adopting gene transfer techniques for tissue engineering is a relatively novel approach, as non-viral gene delivery vectors are continually optimized for therapeutic purposes, and reservations about viral vectors have increasingly dampened their appeal. However, every element involved in gene transfection (i.e., the cell, vector and gene) is a variable which decides the physiological and biomechanical properties of the cartilage produced, and significant work still needs to be done in understanding the contribution of each of these factors to cartilage regeneration. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:592 / 603
页数:12
相关论文
共 52 条
[1]
Adachi N, 2002, J RHEUMATOL, V29, P1920
[2]
Alvarez J, 2002, DEVELOPMENT, V129, P1913
[3]
Apparailly F, 1998, J IMMUNOL, V160, P5213
[4]
Bachmann G, 2004, RADIOLOGE, V44, P773, DOI 10.1007/s00117-004-1084-y
[5]
Prevention of murine collagen-induced arthritis in the knee and ipsilateral paw by local expression of human interleukin-1 receptor antagonist protein in the knee [J].
Bakker, AC ;
Joosten, LAB ;
Arntz, OJ ;
Helsen, MMA ;
Bendele, AM ;
vandeLoo, FAJ ;
vandenBerg, WB .
ARTHRITIS AND RHEUMATISM, 1997, 40 (05) :893-900
[6]
Overexpression of active TGF-beta-1 in the murine knee joint: evidence for synovial-layer-dependent chondro-osteophyte formation [J].
Bakker, AC ;
van de Loo, FAJ ;
van Beuningen, HM ;
Sime, P ;
van Lent, PLEM ;
van der Kraan, PM ;
Richards, CD ;
van den Berg, WB .
OSTEOARTHRITIS AND CARTILAGE, 2001, 9 (02) :128-136
[7]
Transplantation of adenovirally transduced allogeneic chondrocytes into articular cartilage defects in vivo [J].
Baragi, VM ;
Renkiewicz, RR ;
Qiu, LP ;
Brammer, D ;
Riley, JM ;
Sigler, RE ;
Frenkel, SR ;
Amin, A ;
Abramson, SB ;
Roessler, BJ .
OSTEOARTHRITIS AND CARTILAGE, 1997, 5 (04) :275-282
[8]
Bessis N, 1999, CLIN EXP IMMUNOL, V117, P376
[9]
Bolen J., 2005, Morbidity and Mortality Weekly Report, V54, P119
[10]
Dinser R, 2001, HISTOCHEM CELL BIOL, V116, P69