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{"title":"Uncompensated Polychromatic Analysis of Mitochondrial Membrane Potential Using JC-1 and Multilaser Excitation","authors":"Sara De Biasi, Lara Gibellini, Andrea Cossarizza","doi":"10.1002/0471142956.cy0732s72","DOIUrl":null,"url":null,"abstract":"<p>The lipophilic cation JC-1 (5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethyl-benzimidazolyl carbocyanine iodide) has been used for more than 20 years as a specific dye for measuring mitochondrial membrane potential (ΔΨ<sub>m</sub>). In this unit, we revise our original protocol (that made use of a single 488 nm laser for the detection of monomers and aggregates, and where compensation was an important step) to use dual-laser excitation. Moreover, thanks to recently developed multilaser instruments and novel probes for surface and intracellular markers, JC-1 can be utilized by polychromatic flow cytometry to simultaneously detect, without any compensation between fluorescences, ΔΨ<sub>m</sub> along with other biological parameters, such as apoptosis and the production of reactive oxygen species. © 2015 by John Wiley & Sons, Inc.</p>","PeriodicalId":11020,"journal":{"name":"Current Protocols in Cytometry","volume":"72 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/0471142956.cy0732s72","citationCount":"42","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cytometry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/0471142956.cy0732s72","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Health Professions","Score":null,"Total":0}
引用次数: 42
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Abstract
The lipophilic cation JC-1 (5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethyl-benzimidazolyl carbocyanine iodide) has been used for more than 20 years as a specific dye for measuring mitochondrial membrane potential (ΔΨm ). In this unit, we revise our original protocol (that made use of a single 488 nm laser for the detection of monomers and aggregates, and where compensation was an important step) to use dual-laser excitation. Moreover, thanks to recently developed multilaser instruments and novel probes for surface and intracellular markers, JC-1 can be utilized by polychromatic flow cytometry to simultaneously detect, without any compensation between fluorescences, ΔΨm along with other biological parameters, such as apoptosis and the production of reactive oxygen species. © 2015 by John Wiley & Sons, Inc.
利用JC-1和多激光激发对线粒体膜电位进行无补偿多色分析
亲脂性阳离子JC-1(5,5 ',6,6 ' -四氯-1,1 ',3,3 ' -四乙基-苯并咪唑基碘化碳氰)作为测定线粒体膜电位的特定染料已经使用了20多年(ΔΨm)。在本单元中,我们修改了原来的方案(使用单个488nm激光检测单体和聚集体,其中补偿是一个重要步骤),使用双激光激发。此外,由于最近开发了用于表面和细胞内标记物的多激光仪器和新型探针,JC-1可以通过多色流式细胞术同时检测ΔΨm以及其他生物学参数,如凋亡和活性氧的产生,而荧光之间没有任何补偿。©2015 by John Wiley &儿子,Inc。
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