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Assessment of Transfection of AdCMV-EGFP to Rat Submandibular Gland Cells

机译:AdCMV-EGFP转染大鼠下颌下腺细胞的评估

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We evaluated the efficiency of transfecting adenoviral vectors encoding enhanced green fluorescent protein (AdCMV-EGFP) into rat submandibular gland cells and the effects of gene transfer on cell proliferation and secretory function. Isolated submandibular gland cells were transfected with different titers (or multiplicity of infection, MOI) of AdCMV-EGFP. The transfection efficiency was evaluated by quantifying EGFP-positive cells by inverted fluorescence microscopy, cell proliferation by MTT assay, and cell secretory activity by measuring alpha-amylase in culture medium. A transfection efficiency of up to 70.8 % was achieved in submandibular gland cells. MTT assay showed that increased viral titers resulted in significant inhibition of cell proliferation, which occurs on day 5 post-transfection. Simultaneously, the amylase levels started to reduce with a significant decrease on day 7 after transfection. The results show that AdCMV-EGFP transfection of submandibular gland cells at higher MOI results in cytotoxicity, decreased cell proliferation, and secretory function. However, the lower adenoviral titers (e.g., 200 particles/cell) could be an efficient and safe labeling tool for gene transfer to submandibular gland cells.
机译:我们评估了将编码增强型绿色荧光蛋白(AdCMV-EGFP)的腺病毒载体转染至大鼠下颌下腺细胞的效率以及基因转移对细胞增殖和分泌功能的影响。用不同滴度(或感染复数,MOI)的AdCMV-EGFP转染分离的颌下腺细胞。通过倒置荧光显微镜定量EGFP阳性细胞,通过MTT分析测定细胞增殖以及通过测量培养基中的α-淀粉酶来评估细胞分泌活性,从而评估转染效率。下颌下腺细胞的转染效率高达70.8%。 MTT测定表明,病毒滴度的增加导致细胞增殖的明显抑制,这发生在转染后第5天。同时,转染后第7天,淀粉酶水平开始下降,且显着下降。结果表明,以较高的MOI转染下颌下腺细胞的AdCMV-EGFP会导致细胞毒性,降低细胞增殖和分泌功能。但是,较低的腺病毒滴度(例如200个颗粒/细胞)可能是将基因转移至下颌下腺细胞的有效且安全的标记工具。

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