Epstein M, Norman A, Pinkel D, Udkoff R
J Histochem Cytochem. 1977 Jul;25(7):821-6. doi: 10.1177/25.7.70456.
We have adapted a multiparameter cell sorter to measure the distribution of fluorescence polarization in cell populations. Measurements carried out on EL4 cells show that the percent polarization of fluorescein fluorescence decreases with increasing fluorescence intensity. This inverse relationship between polarization and intensity is shown both within the cell population and by the average values of the two quantities during both the increase and decrease of fluorescence intensity. The quantitative relation between intensity and polarization is different in hypertonic than in isotonic media. These results suggest that polarization measurements carried out at a fixed time after incubation of cells with fluorescein diacetate, which is converted to fluorescein within the cells, may depend in part on the rate of fluorescein accumulation, and that agents that have been reported to change the polarization of fluorescein in living cells may do so by changing the kinetics of fluorescein accumulation.
我们采用了一种多参数细胞分选仪来测量细胞群体中荧光偏振的分布。对EL4细胞进行的测量表明,随着荧光强度的增加,荧光素荧光的偏振百分比降低。这种偏振与强度之间的反比关系在细胞群体内部以及荧光强度增加和降低过程中这两个量的平均值中均有体现。在高渗介质中,强度与偏振之间的定量关系与等渗介质中的不同。这些结果表明,在用二乙酸荧光素孵育细胞(二乙酸荧光素在细胞内转化为荧光素)后在固定时间进行的偏振测量可能部分取决于荧光素的积累速率,并且据报道能改变活细胞中荧光素偏振的试剂可能是通过改变荧光素积累的动力学来实现的。