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腺相关病毒载体对牙周膜细胞和人牙龈成纤维细胞的高效基因转移

Efficient gene transfer to periodontal ligament cells and human gingival fibroblasts by adeno-associated virus vectors.

作者信息

Kunze Melanie, Huber Anke, Krajewski Anna, Lowden Esther, Schuhmann Natascha, Buening Hildegard, Hallek Michael, Noack Michael, Perabo Luca

机构信息

Center of Dental Medicine, Department of Operative Dentistry and Periodontology, University of Cologne, Germany.

出版信息

J Dent. 2009 Jul;37(7):502-8. doi: 10.1016/j.jdent.2009.03.001. Epub 2009 Apr 11.

Abstract

OBJECTIVES

We explored for the first time the possibility to deliver a reporter gene (Green Fluorescence Protein) to human primary periodontal ligament (PDL) cells and human gingival fibroblasts (HGF) using shuttle vectors derived from adeno-associated virus (AAV). Since AAV transduction rates on other human primary fibroblasts have been previously shown to depend on the particular cell lineage and on the employed viral serotype, we determined the most effective AAV variant for periodontal cells comparing different vector types.

METHODS

AAV serotypes 1-5 encoding GFP in single stranded (ss) and self-complementary (sc) vector genome conformations were used to infect primary HGF and PDL cells. Two days post-infection, the percentage of GFP expressing cells was determined by flow cytometry.

RESULTS

Highest transduction rates for both cell types were achieved with self-complementary vectors derived from AAV-2, resulting in GFP expression in up to 86% of PDL cells and 50% of HGF. Transgene expression could be observed by optical microscopy for 2 months after infection. Lower but detectable rates were obtained with serotypes 1, 3 and 5.

CONCLUSIONS

The efficacy demonstrated here and the safety and versatility of AAV technology indicated in previous studies clearly suggest the potential of AAV vectors as tools for gene transfer to periodontal tissues.

摘要

目的

我们首次探索了使用源自腺相关病毒(AAV)的穿梭载体将报告基因(绿色荧光蛋白)递送至人原代牙周膜(PDL)细胞和人牙龈成纤维细胞(HGF)的可能性。由于先前已表明AAV对其他人类原代成纤维细胞的转导率取决于特定的细胞谱系和所使用的病毒血清型,因此我们通过比较不同载体类型来确定对牙周细胞最有效的AAV变体。

方法

使用在单链(ss)和自互补(sc)载体基因组构象中编码GFP的AAV血清型1-5来感染原代HGF和PDL细胞。感染后两天,通过流式细胞术确定表达GFP的细胞百分比。

结果

源自AAV-2的自互补载体对两种细胞类型均实现了最高的转导率,导致高达86%的PDL细胞和50%的HGF中表达GFP。感染后2个月通过光学显微镜可观察到转基因表达。血清型1、3和5获得的转导率较低但可检测到。

结论

此处证明的疗效以及先前研究中表明的AAV技术的安全性和多功能性清楚地表明AAV载体作为基因转移至牙周组织的工具的潜力。

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