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与细胞核相关的质粒而非与细胞相关的质粒,与培养的哺乳动物细胞中的转基因表达相关。

Nuclear-associated plasmid, but not cell-associated plasmid, is correlated with transgene expression in cultured mammalian cells.

作者信息

James M B, Giorgio T D

机构信息

Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, USA.

出版信息

Mol Ther. 2000 Apr;1(4):339-46. doi: 10.1006/mthe.2000.0054.

Abstract

Intracellular plasmid is rapidly incorporated into the nucleus of HeLa cells following cationic lipoplex transfection. CV1 cells are less effective in translocating plasmid to the nucleus and also express less transgene than HeLa cells. Cultured HeLa and CV1 cells and corresponding isolated nuclei were analyzed after transfection of a Cy3-labeled pGreenLantern plasmid (Cy3-pGL). Flow cytometry was used to measure both plasmid delivery and transgene expression from the plasmid encoding a CMV promoter-driven green fluorescent protein. During transfection, HeLa cells rapidly incorporated the plasmid, reaching a maximum of 80% Cy3-pGL positive cells 8 h posttransfection. The average Cy3-pGL-positive HeLa cell contained approximately 2470 plasmid copies. Forty-eight percent of the nuclei isolated from the transfected HeLa cells were positive for the plasmid marker after 8 h. In contrast to HeLa cells, fewer CV1 cells and CV1 nuclei incorporated plasmid DNA with peak transfection occurring after 12 h for 36% of the cells and after 8 h for 12% of the nuclei. However, the average Cy3-pGL-positive CV1 cell did not have a significantly different number of total cellular plasmid copies than the average positive HeLa cell. CV1 nuclei, however, had half as much nuclear associated plasmid as HeLa nuclei. HeLa cells are more efficient than CV1 cells at transporting plasmid from the cytoplasm to the nucleus. This study demonstrates the use of a novel quantitative method to study plasmid transport from the cytoplasm to the nucleus and the effect on transgene expression.

摘要

阳离子脂质体复合物转染后,细胞内质粒迅速进入HeLa细胞核。CV1细胞在将质粒转运至细胞核方面效率较低,并且与HeLa细胞相比,其转基因表达量也较少。用Cy3标记的pGreenLantern质粒(Cy3-pGL)转染HeLa和CV1培养细胞及相应分离的细胞核后进行分析。使用流式细胞术来测量质粒传递以及来自编码巨细胞病毒启动子驱动的绿色荧光蛋白的质粒的转基因表达。转染过程中,HeLa细胞迅速摄取质粒,转染后8小时Cy3-pGL阳性细胞最多达到80%。平均每个Cy3-pGL阳性的HeLa细胞含有约2470个质粒拷贝。转染后8小时,从转染的HeLa细胞中分离的细胞核有48%对质粒标记呈阳性。与HeLa细胞相比,摄取质粒DNA的CV1细胞较少,CV1细胞核也较少,转染峰值出现在12小时后,36%的细胞呈阳性,8小时后12%的细胞核呈阳性。然而,平均每个Cy3-pGL阳性的CV1细胞的总细胞质粒拷贝数与平均阳性HeLa细胞相比没有显著差异。然而,CV1细胞核中的核相关质粒只有HeLa细胞核的一半。HeLa细胞在将质粒从细胞质转运至细胞核方面比CV1细胞更有效。本研究展示了一种新型定量方法的应用,用于研究质粒从细胞质到细胞核的转运以及对转基因表达的影响。

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