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A cost-effective method to enhance adenoviral transduction of primary murine osteoblasts and bone marrow stromal cells

机译:增强原代鼠成骨细胞和骨髓基质细胞腺病毒转导的经济有效方法

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摘要

We report here a method for the use of poly-l-lysine (PLL) to markedly improve the adenoviral transduction efficiency of primary murine osteoblasts and bone marrow stromal cells (BMSCs) in culture and in situ, which are typically difficult to transduce. We show by fluorescence microscopy and flow cytometry that the addition of PLL to the viral-containing medium significantly increases the number of green fluorescence protein (GFP)-positive osteoblasts and BMSCs transduced with an enhanced GFP-expressing adenovirus. We also demonstrate that PLL can greatly enhance the adenoviral transduction of osteoblasts and osteocytes in situ in ex vivo tibia and calvaria, as well as in long bone fragments. In addition, we validate that PLL can improve routine adenoviral transduction studies by permitting the use of low multiplicities of infection to obtain the desired biologic effect. Ultimately, the use of PLL to facilitate adenoviral gene transfer in osteogenic cells can provide a cost-effective means of performing efficient gene transfer studies in the context of bone research.
机译:我们在这里报告了一种使用聚-1-赖氨酸(PLL)来显着提高原代鼠成骨细胞和骨髓基质细胞(BMSCs)在培养和原位(通常难以转导)的腺病毒转导效率的方法。我们通过荧光显微镜和流式细胞仪表明,向含病毒的培养基中添加PLL会显着增加绿色荧光蛋白(GFP)阳性成骨细胞和BMSCs的数量,这些表达是通过表达GFP的腺病毒增强转导的。我们还证明,PLL可以极大地增强离体胫骨和颅盖以及长骨碎片中原位成骨细胞和骨细胞的腺病毒转导。此外,我们验证了PLL可以通过允许使用低感染复数获得所需的生物学效应来改善常规腺病毒转导研究。最终,使用PLL促进成骨细胞中腺病毒基因转移可以在骨骼研究的背景下提供一种经济高效的方法来进行有效的基因转移研究。

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