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{"title":"Mitochondrial Subtype Identification and Characterization","authors":"Joseph R. Daniele, Kartoosh Heydari, Andrew Dillin","doi":"10.1002/cpcy.41","DOIUrl":null,"url":null,"abstract":"<p>Healthy, functional mitochondria are central to many cellular and physiological phenomena, including aging, metabolism, and stress resistance. A key feature of healthy mitochondria is a high membrane potential (Δψ) or charge differential (i.e., proton gradient) between the matrix and inner mitochondrial membrane. Mitochondrial Δψ has been extensively characterized via flow cytometry of intact cells, which measures the average membrane potential within a cell. However, the characteristics of individual mitochondria differ dramatically even within a single cell, and thus interrogation of mitochondrial features at the organelle level is necessary to better understand and accurately measure heterogeneity. Here we describe a new flow cytometric methodology that enables the quantification and classification of mitochondrial subtypes (via their Δψ, size, and substructure) using the small animal model <i>C. elegans</i>. Future application of this methodology should allow research to discern the bioenergetic and mitochondrial component in a number of human disease and aging models, including, <i>C. elegans</i>, cultured cells, small animal models, and human biopsy samples. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":11020,"journal":{"name":"Current Protocols in Cytometry","volume":"85 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcy.41","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cytometry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcy.41","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Health Professions","Score":null,"Total":0}
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Abstract
Healthy, functional mitochondria are central to many cellular and physiological phenomena, including aging, metabolism, and stress resistance. A key feature of healthy mitochondria is a high membrane potential (Δψ) or charge differential (i.e., proton gradient) between the matrix and inner mitochondrial membrane. Mitochondrial Δψ has been extensively characterized via flow cytometry of intact cells, which measures the average membrane potential within a cell. However, the characteristics of individual mitochondria differ dramatically even within a single cell, and thus interrogation of mitochondrial features at the organelle level is necessary to better understand and accurately measure heterogeneity. Here we describe a new flow cytometric methodology that enables the quantification and classification of mitochondrial subtypes (via their Δψ, size, and substructure) using the small animal model C. elegans . Future application of this methodology should allow research to discern the bioenergetic and mitochondrial component in a number of human disease and aging models, including, C. elegans , cultured cells, small animal models, and human biopsy samples. © 2018 by John Wiley & Sons, Inc.
线粒体亚型鉴定与表征
健康、功能性的线粒体是许多细胞和生理现象的核心,包括衰老、新陈代谢和抗逆性。健康线粒体的一个关键特征是高膜电位(Δψ)或基质和线粒体内膜之间的电荷差(即质子梯度)。线粒体Δψ已经通过完整细胞的流式细胞术广泛表征,测量细胞内的平均膜电位。然而,即使在单个细胞内,单个线粒体的特征也存在显著差异,因此在细胞器水平上对线粒体特征的研究对于更好地理解和准确测量异质性是必要的。在这里,我们描述了一种新的流式细胞术方法,可以使用小动物模型秀丽隐杆线虫对线粒体亚型(通过它们的Δψ、大小和亚结构)进行量化和分类。该方法的未来应用将使研究能够在许多人类疾病和衰老模型中识别生物能量和线粒体成分,包括秀丽隐杆线虫、培养细胞、小动物模型和人类活检样本。©2018 by John Wiley &儿子,Inc。
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