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原代软骨细胞的高效非病毒转染

High-efficiency nonviral transfection of primary chondrocytes.

作者信息

Welter Jean F, Solchaga Luis A, Stewart Matthew C

机构信息

Department of Orthopedics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, OH, USA.

出版信息

Methods Mol Med. 2004;100:129-46. doi: 10.1385/1-59259-810-2:129.

Abstract

The introduction of foreign DNA into mammalian cells is an essential investigative tool in molecular biology. Nonviral approaches to transfection offer the advantage of relatively simple vector design, production, and purification and, for tissue engineering applications, avoid many of the potential risks associated with virus-mediated transfection methods. Unfortunately, primary cells, and in particular chondrocytes, are notoriously refractory to conventional transfection approaches, and optimized transfection efficiencies in these cells are extremely low (1-1.5%). In this chapter, we present three protocols that have proved useful in transfecting primary chondrocytes at high efficiency (~70%). The first uses radiofrequency electroporation, a transfection method that frequently works extremely well in cell types that are difficult to transfect. It should be noted that electroporation is not limited to DNA but that essentially any molecule can be introduced into the cell using this approach. In addition to the primary protocol, we present two additional reliable, albeit less efficient backup protocols, the first using exponential decay electroporation and the second FuGENE 6 transfection.

摘要

将外源DNA导入哺乳动物细胞是分子生物学中一项重要的研究工具。非病毒转染方法具有载体设计、生产和纯化相对简单的优点,并且对于组织工程应用而言,避免了许多与病毒介导的转染方法相关的潜在风险。不幸的是,原代细胞,尤其是软骨细胞,对传统转染方法极难转染,并且在这些细胞中优化后的转染效率极低(1%-1.5%)。在本章中,我们介绍三种已被证明可高效(约70%)转染原代软骨细胞的方法。第一种方法是使用射频电穿孔,这是一种在难以转染的细胞类型中经常效果极佳的转染方法。应当注意的是,电穿孔并不局限于DNA,基本上任何分子都可以使用这种方法导入细胞。除了主要方法外,我们还介绍了另外两种可靠但效率较低的备用方法,第一种是使用指数衰减电穿孔,第二种是FuGENE 6转染。

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