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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。

Functionalization of microparticles with mineral coatings enhances non-viral transfection of primary human cells.

机构信息

Department of Biomedical Engineering-University of Wisconsin-Madison, Madison, WI, USA.

Department of Orthopedics and Rehabilitation-University of Wisconsin-Madison, Madison, WI, USA.

出版信息

Sci Rep. 2017 Oct 27;7(1):14211. doi: 10.1038/s41598-017-14153-x.

Abstract

Gene delivery to primary human cells is a technology of critical interest to both life science research and therapeutic applications. However, poor efficiencies in gene transfer and undesirable safety profiles remain key limitations in advancing this technology. Here, we describe a materials-based approach whereby application of a bioresorbable mineral coating improves microparticle-based transfection of plasmid DNA lipoplexes in several primary human cell types. In the presence of these mineral-coated microparticles (MCMs), we observed up to 4-fold increases in transfection efficiency with simultaneous reductions in cytotoxicity. We identified mechanisms by which MCMs improve transfection, as well as coating compositions that improve transfection in three-dimensional cell constructs. The approach afforded efficient transfection in primary human fibroblasts as well as mesenchymal and embryonic stem cells for both two- and three-dimensional transfection strategies. This MCM-based transfection is an advancement in gene delivery technology, as it represents a non-viral approach that enables highly efficient, localized transfection and allows for transfection of three-dimensional cell constructs.

摘要

基因传递到原代人类细胞是生命科学研究和治疗应用都非常关注的技术。然而,基因传递效率低下和不理想的安全性仍然是推进这项技术的关键限制。在这里,我们描述了一种基于材料的方法,通过应用可生物吸收的矿物涂层,改善了几种原代人类细胞类型中小粒子质粒 DNA 脂质体的转染。在存在这些矿物涂层微球(MCM)的情况下,我们观察到转染效率提高了 4 倍,同时细胞毒性降低。我们确定了 MCM 改善转染的机制,以及改善三维细胞构建体中转染的涂层成分。该方法在原代人成纤维细胞以及间充质和胚胎干细胞中都能实现高效的二维和三维转染策略。这种基于 MCM 的转染是基因传递技术的一项进步,因为它代表了一种非病毒方法,能够实现高效、局部的转染,并允许对三维细胞构建体进行转染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c4a/5660152/a17f765bf025/41598_2017_14153_Fig1_HTML.jpg

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