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用于干细胞基因工程的非病毒基因转染技术。

Non-viral gene transfection technologies for genetic engineering of stem cells.

作者信息

Jo Jun-ichiro, Tabata Yasuhiko

机构信息

Department of Biomaterials, Field of Tissue Engineering, Institute for Frontier Medical Sciences, Kyoto University, 53 Kawara-cho Shogoin, Sakyo-ku, Kyoto, Japan.

出版信息

Eur J Pharm Biopharm. 2008 Jan;68(1):90-104. doi: 10.1016/j.ejpb.2007.04.021. Epub 2007 Jul 21.

DOI:10.1016/j.ejpb.2007.04.021
PMID:17870447
Abstract

The recent rapid progress of molecular biology together with the steady progress of genome projects has given us some essential and revolutionary information about DNA and RNA to elucidate various biological phenomena at a genetic level. Under these circumstances, the technology and methodology of gene transfection have become more and more important to enhance the efficacy of gene therapy for several diseases. In addition, gene transfection is a fundamental technology indispensable to the further research development of basic biology and medicine regarding stem cells. Stem cells genetically manipulated will enhance the therapeutic efficacy of cell transplantation. In this paper, the carrier and technology of gene delivery are briefly overviewed while the applications to the basic researches of biology and medicine as well as regenerative medical therapy are introduced. A new non-viral carrier and the cell culture system are described to efficiently manipulate stem cells.

摘要

近年来,分子生物学的迅速发展以及基因组计划的稳步推进,为我们提供了一些关于DNA和RNA的重要且具有革命性的信息,以便在基因层面阐明各种生物学现象。在这种情况下,基因转染技术和方法对于提高多种疾病的基因治疗效果变得越来越重要。此外,基因转染是基础生物学和医学关于干细胞进一步研究发展不可或缺的一项基础技术。经过基因操作的干细胞将提高细胞移植的治疗效果。本文简要概述了基因递送的载体和技术,同时介绍了其在生物学和医学基础研究以及再生医学治疗中的应用。还描述了一种新型非病毒载体和细胞培养系统,以有效操控干细胞。

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Non-viral gene transfection technologies for genetic engineering of stem cells.用于干细胞基因工程的非病毒基因转染技术。
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A challenge for regenerative medicine: proper genetic programming, not cellular mimicry.再生医学面临的一项挑战:恰当的基因编程,而非细胞模仿。
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Biomaterial-based delivery systems of nucleic acid for regenerative research and regenerative therapy.用于再生研究和再生治疗的基于生物材料的核酸递送系统。
Regen Ther. 2019 Jul 11;11:123-130. doi: 10.1016/j.reth.2019.06.007. eCollection 2019 Dec.
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Functionalization of microparticles with mineral coatings enhances non-viral transfection of primary human cells.
通过用矿物涂层对微颗粒进行功能化处理,可以增强对原代人类细胞的非病毒转染。
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CRISPR-Cas9 directed knock-out of a constitutively expressed gene using lance array nanoinjection.利用长矛阵列纳米注射技术通过CRISPR-Cas9定向敲除组成型表达基因。
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In vitro efficient transfection by CM₁₈-Tat₁₁ hybrid peptide: a new tool for gene-delivery applications.CM₁₈-Tat₁₁ 杂合肽的体外高效转染:基因传递应用的新工具。
PLoS One. 2013 Jul 29;8(7):e70108. doi: 10.1371/journal.pone.0070108. Print 2013.
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