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Non-viral gene delivery to mesenchymal stem cells: methods, strategies and application in bone tissue engineering and regeneration.

机译:非病毒基因传递到间充质干细胞:方法,策略和骨组织工程和再生中的应用。

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摘要

Mesenchymal stem cells (MSCs) can be isolated from several tissues in the body, have the ability to self-renewal, show immune suppressive properties and are multipotent, being able to generate various cell types. At present, due to their intrinsic characteristics, MSCs are considered very promising in the area of tissue engineering and regenerative medicine. In this context, genetic modification can be a powerful tool to control the behavior and fate of these cells and be used in the design of new cellular therapies. Viral systems are very effective in the introduction of exogenous genes inside MSCs. However, the risks associated with their use are leading to an increasing search for non-viral approaches to attain the same purpose, even if MSCs have been shown to be more difficult to transfect in this way. In the past few years, progress was made in the development of chemical and physical methods for non-viral gene delivery. Herein, an overview of the application of those methods specifically to MSCs is given and their use in tissue engineering and regenerative medicine therapeutic strategies highlighted using the example of bone tissue. Key issues and future directions in non-viral gene delivery to MSCs are also critically addressed.
机译:间充质干细胞(MSC)可以从体内的几个组织中分离出来,具有自我更新的能力,显示出免疫抑制特性,并且具有多能性,能够产生多种细胞类型。目前,由于其固有特性,MSC被认为在组织工程和再生医学领域非常有前途。在这种情况下,基因修饰可以成为控制这些细胞的行为和命运的强大工具,并可以用于设计新的细胞疗法。病毒系统在将外源基因引入MSC内部非常有效。但是,与使用它们有关的风险导致人们越来越多地寻求非病毒方法来达到相同的目的,即使已证明MSC难以以这种方式进行转染。在过去的几年中,在非病毒基因递送的化学和物理方法的开发方面取得了进展。在此,概述了这些方法在MSCs中的应用,并以骨组织为例突出了它们在组织工程和再生医学治疗策略中的应用。关键问题和非病毒基因传递给MSC的未来方向也得到了关键解决。

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