Reston J T, Gould-Fogerite S, Mannino R J
Department of Biomedical Sciences, School of Public Health, Empire State Plaza, Albany, New York 12201-0509, USA.
Mol Cell Biochem. 1995 Apr 26;145(2):169-75. doi: 10.1007/BF00935489.
Cellular physiology has a significant influence on the efficiency of various gene transfer procedures, as shown by the fact that transfection efficiency varies dramatically among different cell lines. However, the aspects of cellular physiology which influence the transfection process remain substantially uncharacterized. In this study, NIH3T3 cells were treated with inhibitors of protein synthesis, DNA synthesis, and RNA synthesis to determine the importance of these processes in the calcium-phosphate transfection process. The results suggest that protein synthesis during the first 4 h after DNA addition enhances transfection. In contrast, inhibition of RNA synthesis has no effect on transfection during the first 24 h post-DNA addition. The DNA synthesis inhibitor results remain inconclusive due to a secondary inhibition of an unknown cellular factor. Secondly, agents that destabilize microtubules, microfilaments, and the golgi apparatus were used to determine whether these elements play a role in the transfection process. The results suggest that microtubules are not involved in the transfection process, microfilaments are important but not necessary for the transfection process, and a functional golgi apparatus is essential early in the transfection process. These studies provide a foundation from which further investigations into the cellular processes involved in the uptake and expression of exogenous DNA can proceed.
细胞生理学对各种基因转移程序的效率有重大影响,不同细胞系之间转染效率差异巨大这一事实就表明了这一点。然而,影响转染过程的细胞生理学方面仍基本未被阐明。在本研究中,用蛋白质合成、DNA合成和RNA合成抑制剂处理NIH3T3细胞,以确定这些过程在磷酸钙转染过程中的重要性。结果表明,添加DNA后的前4小时内进行蛋白质合成可提高转染效率。相比之下,添加DNA后的前24小时内抑制RNA合成对转染没有影响。由于对一种未知细胞因子的二次抑制作用,DNA合成抑制剂的结果尚无定论。其次,使用能破坏微管、微丝和高尔基体稳定性的试剂来确定这些成分在转染过程中是否起作用。结果表明,微管不参与转染过程,微丝对转染过程很重要但并非必需,且在转染早期高尔基体的功能至关重要。这些研究为进一步研究参与外源DNA摄取和表达的细胞过程奠定了基础。