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使用吖啶橙对溶酶体膜通透性进行实时监测。

Real-Time Monitoring of Lysosomal Membrane Permeabilization Using Acridine Orange.

作者信息

Eriksson Ida, Vainikka Linda, Persson Hans Lennart, Öllinger Karin

机构信息

Experimental Pathology, Department of Biomedical and Clinical Sciences, Linköping University, 581 85 Linköping, Sweden.

Department of Respiratory Medicine in Linköping, Linköping University, 581 85 Linköping, Sweden.

出版信息

Methods Protoc. 2023 Aug 9;6(4):72. doi: 10.3390/mps6040072.

Abstract

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.

摘要

溶酶体膜完整性的丧失会导致溶酶体水解酶泄漏到细胞质中,这可能会损害细胞功能并诱导细胞死亡。溶酶体的不稳定通常先于凋亡或坏死性细胞死亡,并且在生理和病理条件下都会发生。弱碱吖啶橙很容易进入细胞并积聚在溶酶体的酸性环境中。用吖啶橙进行活细胞染色是一种经过充分验证的技术,可使用荧光显微镜和流式细胞术观察溶酶体的不稳定情况。然而,这些分析耗时且仅适用于离散的时间点,这使得它们不适合大规模研究。因此,我们开发了一种省时、高通量的基于微孔板读数器的方法,以实时跟踪使用吖啶橙的溶酶体膜的不稳定情况。由于每个样品的细胞数量少且分析时间短,该方案可以很容易地应用于患者样品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/646b/10459729/cdd507ffdf1f/mps-06-00072-g001.jpg

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