Panusatid Chatnapa, Thangsiriskul Nattachai, Peerapittayamongkol Chayanon
Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
MethodsX. 2022 Apr 2;9:101685. doi: 10.1016/j.mex.2022.101685. eCollection 2022.
Mitochondria are important organelles responsible for energy production. Mitochondrial dysfunction relates to various pathological diseases. The investigation of mitochondrial heath is critical to evaluate the cellular status. Herein, we demonstrated an approach for determining the status of mitochondrial health by observing mitochondrial HO (one type of ROS), membrane potential, and morphology (fragmentation and length) in live primary fibroblast cells. The cells were co-stained with fluorescent dyes (Hoechst 33342 and MITO-ID® Red/MitoPY1/JC-10) and continuously processed by the High Content Imaging System. We employed the Operetta CLS to take fluorescent images with its given quickness and high resolution. The CellProfiler image analysis software was further used to identify cell and mitochondrial phenotypes in the thousand fluorescent images.•We could quantitatively analyze fluorescent images with high-throughput and high-speed detection to track the alteration of mitochondrial status.•The MMP assay is sensitive to FCCP even at the concentration of 0.01 µM.•The fibroblast cells treated with stress inducers (HO, FCCP, and phenanthroline) revealed a significant change in mitochondrial health parameters, with more ROS accumulation, depolarized MMP, increased fragmentation, and reduced length of mitochondria.
线粒体是负责能量产生的重要细胞器。线粒体功能障碍与多种病理疾病相关。线粒体健康状况的研究对于评估细胞状态至关重要。在此,我们展示了一种通过观察活的原代成纤维细胞中线粒体HO(一种活性氧)、膜电位和形态(碎片化和长度)来确定线粒体健康状态的方法。细胞用荧光染料(Hoechst 33342和MITO-ID® Red/MitoPY1/JC-10)进行共染色,并通过高内涵成像系统连续处理。我们使用Operetta CLS以其给定的速度和高分辨率拍摄荧光图像。进一步使用CellProfiler图像分析软件在数千张荧光图像中识别细胞和线粒体表型。
•我们可以通过高通量和高速检测对荧光图像进行定量分析,以跟踪线粒体状态的变化。
•即使在0.01 µM的浓度下,MMP检测对FCCP也很敏感。
•用应激诱导剂(HO、FCCP和菲咯啉)处理的成纤维细胞显示线粒体健康参数有显著变化,活性氧积累更多、MMP去极化、碎片化增加且线粒体长度缩短。