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软骨组织工程的基因递送策略。

Gene delivery strategies for cartilage tissue engineering.

作者信息

Saraf Anita, Mikos Antonios G

机构信息

Department of Bioengineering, Rice University, P.O. Box 1892, MS 142, Houston, TX 77251-1892, USA.

出版信息

Adv Drug Deliv Rev. 2006 Jul 7;58(4):592-603. doi: 10.1016/j.addr.2006.03.005.

Abstract

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.

摘要

组织工程是一项多方面的技术,其开发目的是再生复杂组织和器官。软骨再生一直是工程师们面临的挑战,新一轮的努力集中在开发通过生长因子和其他生物分子为细胞提供持续刺激以促进其分化为软骨细胞的策略。尽管大量研究致力于开发直接递送生长因子的控释系统,但解决这一困境的一种更简单方法是将细胞转化为蛋白质生产工厂。这是通过基因递送实现的。针对类风湿性关节炎和骨关节炎等关节疾病发表的基因治疗研究提供了有关不同类型细胞、基因递送载体和可能用于软骨再生的基因的宝贵信息。组织工程方法提供了将迄今为止用于基因治疗的两种或更多种策略结合起来并创建一个同时解决软骨退变和合成问题的连贯系统的机会。将基因转移技术应用于组织工程是一种相对新颖的方法,因为非病毒基因递送载体不断针对治疗目的进行优化,而对病毒载体的保留意见越来越削弱了它们的吸引力。然而,基因转染中涉及的每个要素(即细胞、载体和基因)都是决定所产生软骨的生理和生物力学特性的变量,在理解这些因素各自对软骨再生的贡献方面仍有大量工作要做。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94ea/2702530/5194f6ba40d1/nihms17707f1.jpg

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Orthopaedic applications of gene therapy.
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