Separation of cells expressed specific antigen on the surface based on dielectrophoresis

T. Yasukawa, F. Mizutani
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引用次数: 1

Abstract

Rapid conversion of the line formation with the cells based on dielectrophoresis (DEP) was applied to simple and rapid distinction of cells with specific surface antigens from a cell population. The gap area of the interdigitated band array (IDA) electrode was modified with anti-CD33 antibody. Human promyelocytic leukemia cells (HL-60) which express CD33 surface antigen were accumulated on the surface in the gap area between both bands of the IDA electrode by negative DEP (n-DEP). Switching of the applied voltage of the band electrode brought about the removal of accumulated cells to form another pattern due to the formation of the different pattern of the electric field in the device. The modification with the antibody inhibits the removal of the cells with specific surface antigen due to the irreversible capture with immunoreactions during the first pattern formation. Therefore, we should discriminate the cells with specific antigen from the cell remained on the gap area. The time required for the assay was substantially short, 60 s for forcing and 60 s for the separation of unbounded cells. Furthermore, the present method does not require pretreatment such as target labeling or washing of unbound cells.
在介质电泳的基础上分离表面表达特异性抗原的细胞
基于dielectrophoresis (DEP)的细胞系形成快速转化技术可以简单、快速地从细胞群中分离出具有特定表面抗原的细胞。用抗cd33抗体修饰双指间带阵列(IDA)电极的间隙区域。表达CD33表面抗原的人早幼粒细胞白血病细胞(HL-60)通过负DEP (n-DEP)聚集在IDA电极两条带之间的间隙区域表面。由于器件中电场的不同模式的形成,带电极施加电压的切换使积累的电池被移除形成另一种模式。该抗体的修饰抑制了由于在第一模式形成过程中免疫反应的不可逆捕获而导致的具有特定表面抗原的细胞的去除。因此,我们应该将具有特异性抗原的细胞与留在间隙区域的细胞区分开来。实验所需的时间非常短,强制60秒,分离无界细胞60秒。此外,本方法不需要预处理,如靶标标记或洗涤未结合的细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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