吖啶橙实时监测溶酶体膜透性。

IF 2 Q3 BIOCHEMICAL RESEARCH METHODS Methods and Protocols Pub Date : 2023-08-09 DOI:10.3390/mps6040072
Ida Eriksson, Linda Vainikka, Hans Lennart Persson, Karin Öllinger
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引用次数: 3

摘要

溶酶体膜完整性的丧失导致溶酶体水解酶渗漏到细胞质中,这可能损害细胞功能并诱导细胞死亡。溶酶体的失稳通常发生在细胞凋亡或坏死死亡之前,并在生理和病理条件下发生。弱碱吖啶橙很容易进入细胞并在溶酶体的酸性环境中积累。吖啶橙活体染色是一种经过验证的技术,可以使用荧光显微镜和流式细胞术观察溶酶体的不稳定性。然而,这些分析是耗时的,并且只适用于离散时间点,这使得它们不适合大规模的方法。因此,我们开发了一种节省时间,高通量的基于微孔板阅读器的方法,使用吖啶橙实时跟踪溶酶体膜的不稳定。由于每个样本的细胞数量少,分析时间短,因此该方案可以很容易地用于患者样本。
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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Real-Time Monitoring of Lysosomal Membrane Permeabilization Using Acridine Orange.
Loss of lysosomal membrane integrity results in leakage of lysosomal hydrolases to the cytosol which might harm cell function and induce cell death. Destabilization of lysosomes often precede apoptotic or necrotic cell death and occur during both physiological and pathological conditions. The weak base acridine orange readily enters cells and accumulates in the acidic environment of lysosomes. Vital staining with acridine orange is a well-proven technique to observe lysosomal destabilization using fluorescence microscopy and flow cytometry. These analyses are, however, time consuming and only adapted for discrete time points, which make them unsuitable for large-scale approaches. Therefore, we have developed a time-saving, high-throughput microplate reader-based method to follow destabilization of the lysosomal membrane in real-time using acridine orange. This protocol can easily be adopted for patient samples since the number of cells per sample is low and the time for analysis is short.
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来源期刊
Methods and Protocols
Methods and Protocols Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
3.60
自引率
0.00%
发文量
85
审稿时长
8 weeks
期刊最新文献
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