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综述:基于基因和干细胞的骨再生与修复疗法

Review: gene- and stem cell-based therapeutics for bone regeneration and repair.

作者信息

Kimelman Nadav, Pelled Gadi, Helm Gregory A, Huard J, Schwarz Edward M, Gazit Dan

机构信息

Skeletal Biotech Lab, The Hebrew University of Jerusalem-Hadassah Medical Campus, Ein Kerem, Jerusalem, Israel.

出版信息

Tissue Eng. 2007 Jun;13(6):1135-50. doi: 10.1089/ten.2007.0096.

Abstract

Many clinical conditions require regeneration or implantation of bone. This is one focus shared by neurosurgery and orthopedics. Current therapeutic options (bone grafting and protein-based therapy) do not provide satisfying solutions to the problem of massive bone defects. In the past few years, gene- and stem cell-based therapy has been extensively studied to achieve a viable alternative to current solutions offered by modern medicine for bone-loss repair. The use of adult stem cells for bone regeneration has gained much focus. This unique population of multipotential cells has been isolated from various sources, including bone marrow, adipose, and muscle tissues. Genetic engineering of adult stem cells with potent osteogenic genes has led to fracture repair and rapid bone formation in vivo. It is hypothesized that these genetically modified cells exert both an autocrine and a paracrine effects on host stem cells, leading to an enhanced osteogenic effect. The use of direct gene delivery has also shown much promise for in vivo bone repair. Several viral and nonviral methods have been used to achieve substantial bone tissue formation in various sites in animal models. To advance these platforms to the clinical setting, it will be mandatory to overcome specific hurdles, such as control over transgene expression, viral vector toxicity, and prolonged culture periods of therapeutic stem cells. This review covers a prospect of cell and gene therapy for bone repair as well as some very recent advancements in stem cell isolation, genetic engineering, and exogenous control of transgene expression.

摘要

许多临床病症都需要进行骨再生或骨植入。这是神经外科和骨科的一个共同关注点。目前的治疗选择(骨移植和基于蛋白质的疗法)并不能为大面积骨缺损问题提供令人满意的解决方案。在过去几年中,基于基因和干细胞的疗法得到了广泛研究,以寻求一种可行的替代方案,来替代现代医学目前提供的骨丢失修复方法。利用成体干细胞进行骨再生已备受关注。这种独特的多能细胞群体已从包括骨髓、脂肪和肌肉组织在内的各种来源中分离出来。用强效成骨基因对成体干细胞进行基因工程改造已在体内实现骨折修复和快速骨形成。据推测,这些基因改造细胞对宿主干细胞发挥自分泌和旁分泌作用,从而增强成骨效果。直接基因递送在体内骨修复方面也显示出很大前景。几种病毒和非病毒方法已被用于在动物模型的不同部位实现大量骨组织形成。为了将这些平台推进到临床应用,必须克服特定障碍,如对转基因表达的控制、病毒载体毒性以及治疗性干细胞的长时间培养。本综述涵盖了骨修复的细胞和基因疗法前景以及干细胞分离、基因工程和转基因表达的外源控制方面的一些最新进展。

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