Noda Y, Shimizu N, Kawazoe Y
Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.
Biol Pharm Bull. 1996 Dec;19(12):1565-9. doi: 10.1248/bpb.19.1565.
The permeability of murine leukemia L1210 cells toward non-permeant fluorescent Lucifer Yellow (LY) was evaluated by flow cytometry following vortex-stirring of cells with LY in the presence of high molecular weight polyacrylic acid (A-119). Permeabilization by this technique was greatly enhanced in growth phase cells, whereas it was appreciably reduced in resting cells which had been maintained in unchanged culture medium for 2 to 4d. This reduction in permeabilization of resting cells gradually disappeared when resting cells were re-suspended in fresh culture medium, and the degree of permeabilization was restored to that of the growing cells. It is recommended that the mammalian cells used for internalization of non-permeant materials by vortex-stirring with A-119 should be in the early log phase.
在用高分子量聚丙烯酸(A-119)存在的情况下,将小鼠白血病L1210细胞与荧光素黄(LY)涡旋搅拌后,通过流式细胞术评估了其对非渗透性荧光素黄(LY)的通透性。用这种技术进行的通透化在生长阶段的细胞中大大增强,而在已在未更换的培养基中维持2至4天的静止细胞中则明显降低。当将静止细胞重悬于新鲜培养基中时,静止细胞通透化的这种降低逐渐消失,并且通透化程度恢复到生长细胞的水平。建议通过与A-119涡旋搅拌来内化非渗透性物质的哺乳动物细胞应处于对数早期。