Shimizu N, Kawazoe Y
Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.
Biol Pharm Bull. 1996 Aug;19(8):1023-5. doi: 10.1248/bpb.19.1023.
Using a new technique of vortex-stirring of cells with high molecular weight polyacrylic acid (A-119), non-permeant fluorescein isothiocyanate-labeled dextrans (FDs) of various molecular weights were tested to determine the degree of their internalization into cultured murine leukemia L1210 cells. Flow cytometric analyses of the treated cells revealed that FD4 with a molecular weight (MW) of 4400 was incorporated in an amount 13.2 times greater than that of the control and that FDs with MW of 19000 and 38260 were incorporated at levels several times greater than control levels, by vortex-stirring cells with A-119 for 10 s followed by maintenance at 0 degree C for 10 min. Results of the present study indicate that this permeabilization procedure might be useful to introduce poorly permeable materials into cultured mammalian cells, which would be beneficial in various fields of biological research.
利用一种将细胞与高分子量聚丙烯酸(A - 119)进行涡旋搅拌的新技术,对各种分子量的非渗透性异硫氰酸荧光素标记葡聚糖(FDs)进行测试,以确定它们内化进入培养的小鼠白血病L1210细胞的程度。对处理过的细胞进行流式细胞术分析显示,通过将细胞与A - 119涡旋搅拌10秒,然后在0℃下维持10分钟,分子量(MW)为4400的FD4的掺入量比对照高13.2倍,分子量为19000和38260的FDs的掺入水平比对照水平高几倍。本研究结果表明,这种通透化程序可能有助于将低渗透性物质引入培养的哺乳动物细胞,这将在生物研究的各个领域中有益。