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In vitro study for laser gene transfer in 'BHK-21' fibroblast cell line

机译:BHK-21成纤维细胞系中激光基因转移的体外研究

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Modifications to our previously introduced system for laser microbeam cell surgery were carried out in the present work to match animal cells.rnThese modifications included: 1- Using other laser system that used before, Excimer laser with 193 and 308 nm wavelengths. The used laser here, is He-Cd with low power and 441.5 nm wavelength in the visible region. 2- Instead of using pulsed laser, we used here CW He-Cd chopped by electrical chopper, which is synchronized with the mechanical motion of the mobile stage with step 40 microns, according to cell dimensions to avoid puncturing the same cell twice. The advantages of the modified here laser setup for gene transfer is: it is less damaging to the sensitive animal cell which has thin cell membrane.rnThe present work aimed to: 1- Design a modified laser microbeam cell surgery, applicable to animal cells, such as fibroblast cells 2- To examine the efficiency of such system. 3- To assure gene transfer and its expression in the used cells. 4- To evaluate the ultra damages produced from using the laser beam as a modality for gene transfer. On the other wards, to introduce: safe, efficient and less damaging modality for gene transfer in animal cells.rnTo achieve these goals, we applied the introduced here home- made laser setup with its synchronized parameters to introduce pBK-CMV phagemid, containing LacZ and neomycin resistance (neo~r )genes into BHK-21 fibroblast cell line.rnThe results of the present work showed that: 1- Our modified laser microbeam cell surgery setup proved to be useful and efficient tool for gene transfer into fibroblast cells. 2- The presence and expression of LacZ gene was achieved using histochemical LacZ assay. 3- Selection of G418 antibiotic sensitivity assay confirmed the presence and expression towards stability of neo~r gene with time. 4- Presence of LacZ and neo~r genes in the genomic DNA of transfected fibroblast cells was indicated using PCR analysis. 5- Transmission electron microscopy indicated that, no ultradamages or changes for cell; membrane, organilles or any component of transfected fibroblast cell as a result of using laser microbeam compared with control cell.
机译:在本工作中,我们对先前引入的激光微束细胞手术系统进行了修改,以匹配动物细胞。这些修改包括:1-使用以前使用的其他激光系统,波长为193和308 nm的准分子激光器。此处使用的激光器是He-Cd,它具有低功率,在可见光区域的波长为441.5 nm。 2-此处不使用脉冲激光,而是使用通过电斩波器斩波的CW He-Cd,该CW He-Cd与可移动台的机械运动同步,步距为40微米,根据细胞尺寸,以避免刺破同一细胞两次。经改良的此处用于基因转移的激光装置的优点是:它对具有薄细胞膜的敏感动物细胞的损害较小。本工作旨在:1-设计一种适用于动物细胞的改良激光微束细胞手术,例如作为成纤维细胞2-检查这种系统的效率。 3-确保基因转移及其在所用细胞中的表达。 4-评估使用激光束作为基因转移方法所产生的超损伤。在另一方面,我们将介绍:用于动物细胞中基因转移的安全,有效和破坏性较小的方法。为了实现这些目标,我们将此处介绍的自制激光装置及其同步参数应用于包含LacZ的pBK-CMV噬菌粒。本研究结果表明:1-我们改良的激光微束细胞手术装置被证明是将基因转移到成纤维细胞中的有用和有效的工具。 2-使用组织化学LacZ测定法实现了LacZ基因的存在和表达。 3-G418抗生素敏感性试验的选择证实了neo-r基因的存在和表达随时间的推移而趋向稳定。 4-使用PCR分析表明了转染的成纤维细胞的基因组DNA中LacZ和neo-r基因的存在。 5-透射电子显微镜表明,细胞没有超损伤或变化;与对照细胞相比,使用激光微束的结果是转染的成纤维细胞的细胞膜,器官或任何成分。

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