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流动系统中单细胞胞质荧光去极化的测量。

Measurement of cytoplasmic fluorescence depolarization of single cells in a flow system.

作者信息

Price G B, McCutcheon M J, Taylor W B, Miller R G

出版信息

J Histochem Cytochem. 1977 Jul;25(7):597-600. doi: 10.1177/25.7.302266.

Abstract

We have built a flow system in which we can analyze and sort individual viable cells on the basis of their cytoplasmic microviscosity. The average cytoplasmic microviscosity (or cytoplasmic structuredness) of a cell can be quantitated by exciting fluorescein molecules in the cytoplasm of the cell with a polarized light source and measuring the extent of depolarization of the fluorescent signal. Changes in the state of a cell (e.g., the reception of a signal inducing the cell to differentiate) often appear to be associated with changes in cytoplasmic microviscosity, these changes being detectable within hours of the inducing signal. An example of one such change is presented.

摘要

我们构建了一个流动系统,在该系统中,我们可以根据单个活细胞的细胞质微粘度对其进行分析和分选。细胞的平均细胞质微粘度(或细胞质结构)可以通过用偏振光源激发细胞细胞质中的荧光素分子并测量荧光信号的去极化程度来定量。细胞状态的变化(例如,诱导细胞分化的信号的接收)似乎常常与细胞质微粘度的变化相关,这些变化在诱导信号发出后的数小时内即可检测到。本文给出了一个此类变化的例子。

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