载脂蛋白A-I作为绿色荧光蛋白GFP基因转运形式在大鼠肝细胞中的应用

Q4 Biochemistry, Genetics and Molecular Biology Sibirskii nauchnyi meditsinskii zhurnal Pub Date : 2023-08-30 DOI:10.18699/ssmj20230409
L. Polyakov, D. V. Sumenkova, M. V. Kotova, N. V. Trifonova, R. Knyazev
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引用次数: 0

摘要

本研究的目的是研究使用载脂蛋白A-I(apo A-I)作为绿色荧光蛋白(GFP)基因的转运形式进入大鼠肝细胞的可能性。材料和方法。使用分离的大鼠肝细胞的培养物作为模型。通过将Apo A-I蛋白与异硫氰酸荧光素(FITC)在pH 9.5的碳酸盐缓冲液中以每1mg蛋白12.5μg FITC的比例孵育,获得了具有异硫氰酸荧光荧光素的Apo A-I缀合物。用整合的GFP基因转染pE-GAG的质粒在具有CC(GCC)3-5型顺式元件的启动子部分富集,以增强与apo A-I的复合物形成。倒置荧光显微镜用于细胞荧光的视觉分析。结果和讨论。本文提供了FITC标记的apo A-I通过受体介导的内吞作用渗透到大鼠肝细胞的细胞质和细胞核的证据。在此基础上,提出了使用apo A-I作为将具有整合的GFP基因的质粒DNA靶向递送到细胞中的手段的尝试。根据荧光显微镜的结果,使用apo A-I作为质粒DNA转染剂导致GFP蛋白在肝细胞的细胞质中积累。在没有apo A-I的情况下没有观察到荧光蛋白。结论。所获得的结果可能表明GFP基因递送到细胞的核装置,其表达和GFP蛋白的合成。
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The use of apolipoprotein A-I as a transport form of the green fluorescent protein GFP gene in rat hepatocytes
The aim of this study was to investigate the possibility of using apolipoprotein A-I (apo A-I) as a transport form of the green fluorescent protein (GFP) gene into rat hepatocytes.Material and methods. A culture of isolated rat hepatocytes was used as a model. Apo A-I conjugate with fluorescein isothiocyanate (FITC) was obtained by incubation of apo A-I protein with FITC in carbonate buffer pH 9.5 at a ratio of 12.5 μg FITC per 1 mg of protein. Plasmids for pE-GAG transfection with an integrated GFP gene were enriched in the promoter part with cis-elements of the CC(GCC)3-5 type to enhance complex formation with apo A-I. An inverted fluorescence microscope was used for visual analysis of cell fluorescence.Results and discussion. The paper presents evidence of FITC-labeled apo A-I penetration into the cytoplasm and nuclei of rat hepatocytes by receptor-mediated endocytosis. On this basis, it is proposed an attempt to use apo A-I as a means of targeted delivery of plasmid DNA with an integrated GFP gene into the cell. According to the results of fluorescence microscopy, the use of apo A-I as a plasmid DNA transfection agent led to the accumulation of the GFP protein in the cytoplasm of hepatocytes. No fluorescent protein was observed in the absence of apo A-I.Conclusions. The result obtained may indicate the delivery of the GFP gene to the nuclear apparatus of the cell, its expression and GFP protein synthesis.
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0.40
自引率
0.00%
发文量
54
审稿时长
12 weeks
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