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基于基因的关节软骨修复方法。

Gene-based approaches for the repair of articular cartilage.

作者信息

Trippel S B, Ghivizzani S C, Nixon A J

机构信息

Department of Orthopaedic Surgery, University of Indiana Medical School, Indianapolis, IN, USA.

出版信息

Gene Ther. 2004 Feb;11(4):351-9. doi: 10.1038/sj.gt.3302201.

Abstract

Gene transfer technology has opened novel treatment avenues toward the treatment of damaged musculoskeletal tissues, and may be particularly beneficial to articular cartilage. There is no natural repair mechanism to heal damaged or diseased cartilage. Existing pharmacologic, surgical and cell based treatments may offer temporary relief but are incapable of restoring damaged cartilage to its normal phenotype. Gene transfer provides the capability to achieve sustained, localized presentation of bioactive proteins or gene products to sites of tissue damage. A variety of cDNAs have been cloned which may be used to stimulate biological processes that could improve cartilage healing by (1) inducing mitosis and the synthesis and deposition of cartilage extracellular matrix components by chondrocytes, (2) induction of chondrogenesis by mesenchymal progenitor cells, or (3) inhibiting cellular responses to inflammatory stimuli. The challenge is to adapt this technology into a useful clinical treatment modality. Using different marker genes, the principle of gene delivery to synovium, chondrocytes and mesenchymal progenitor cells has been convincingly demonstrated. Following this, research efforts have begun to move to functional studies. This involves the identification of appropriate gene or gene combinations, incorporation of these cDNAs into appropriate vectors and delivery to specific target cells within the proper biological context to achieve a meaningful therapeutic response. Methods currently being explored range from those as simple as direct delivery of a vector to a cartilage defect, to synthesis of cartilaginous implants through gene-enhanced tissue engineering. Data from recent efficacy studies provide optimism that gene delivery can be harnessed to guide biological processes toward both accelerated and improved articular cartilage repair.

摘要

基因转移技术为受损肌肉骨骼组织的治疗开辟了新的途径,对关节软骨可能特别有益。受损或患病的软骨没有自然修复机制。现有的药物、手术和基于细胞的治疗方法可能只能提供暂时缓解,但无法将受损软骨恢复到正常表型。基因转移能够将生物活性蛋白或基因产物持续、局部地递送至组织损伤部位。多种互补DNA(cDNA)已被克隆,可用于刺激生物过程,从而通过以下方式改善软骨愈合:(1)诱导软骨细胞的有丝分裂以及软骨细胞外基质成分的合成与沉积;(2)诱导间充质祖细胞向软骨细胞分化;或(3)抑制细胞对炎症刺激的反应。挑战在于将这项技术转化为一种有效的临床治疗方式。利用不同的标记基因,已令人信服地证明了向滑膜、软骨细胞和间充质祖细胞进行基因递送的原理。在此之后,研究工作已开始转向功能研究。这涉及确定合适的基因或基因组合,将这些cDNA整合到合适的载体中,并在适当的生物学环境下递送至特定靶细胞,以实现有意义的治疗反应。目前正在探索的方法范围很广,从简单地将载体直接递送至软骨缺损部位,到通过基因增强组织工程合成软骨植入物。近期疗效研究的数据让人乐观地认为,基因递送可用于引导生物过程,以加速和改善关节软骨修复。

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