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通过非病毒基因递送对间充质干细胞进行基因工程改造。

Genetic engineering of mesenchymal stem cells by non-viral gene delivery.

作者信息

Wang Weiwei, Xu Xun, Li Zhengdong, Lendlein Andreas, Ma Nan

机构信息

Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany.

Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany Helmholtz Virtual Institute - Multifunctional Materials in Medicine, Berlin and Teltow, Germany.

出版信息

Clin Hemorheol Microcirc. 2014;58(1):19-48. doi: 10.3233/CH-141883.

Abstract

Mesenchymal stem cells (MSCs) are an ideal cell source for tissue engineering and regenerative medicine as they possess self-renewal properties and multilineage differentiation potential. They can be isolated from various tissues and expanded easily through normal cell culture techniques. Genetic modifications of MSCs to further improve their therapeutic efficacy have been widely studied and extensively researched. Compared to viral gene delivery methods, non-viral methods generate less toxicity and immunogenicity and thus represent a promising and effective tool for the genetic engineering of MSCs. In the last decades, various non-viral gene delivery strategies have been developed and some of them have been applied for MSC transfection. This paper gives an overview of the techniques, influencing factors and potential applications of non-viral methods used for the genetic engineering of MSCs.

摘要

间充质干细胞(MSCs)是组织工程和再生医学的理想细胞来源,因为它们具有自我更新特性和多向分化潜能。它们可以从各种组织中分离出来,并通过常规细胞培养技术轻松扩增。对MSCs进行基因改造以进一步提高其治疗效果已得到广泛研究。与病毒基因递送方法相比,非病毒方法产生的毒性和免疫原性较小,因此是MSCs基因工程的一种有前景且有效的工具。在过去几十年中,已开发出各种非病毒基因递送策略,其中一些已应用于MSCs转染。本文概述了用于MSCs基因工程的非病毒方法的技术、影响因素和潜在应用。

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