Chacko Leeba Ann, Ananthanarayanan Vaishnavi
Centre for BioSystems Science and Engineering, Indian Institute of Science, Bangalore 560012, India.
Bio Protoc. 2019 Dec 5;9(23):e3450. doi: 10.21769/BioProtoc.3450.
Mitochondria are double-membraned organelles responsible for several functions in the cell including energy production, calcium signaling, and cellular metabolism. An equilibrium between fission and fusion events of mitochondria is required for their proper functioning. Mitochondrial morphologies have been quantified in yeast using image processing modules such as MitoGraph and MitoLoc. However, the dynamics of mitochondrial fission and fusion have not been analyzed in these methods. Here, we present a method for measuring mitochondrial morphologies, as well as estimation of fission and fusion frequencies of mitochondria in individual fission yeast cells whose mitochondria are fluorescently-tagged or stained. The latter relies on counting of individual mitochondria upon signal filtering in each frame of a time-lapse. Taken together, we present a simple protocol for analyzing mitochondrial dynamics, which can easily be adopted to other model systems.
线粒体是具有双层膜的细胞器,负责细胞内的多种功能,包括能量产生、钙信号传导和细胞代谢。线粒体的正常功能需要其裂变和融合事件之间保持平衡。在酵母中,已使用诸如MitoGraph和MitoLoc等图像处理模块对线粒体形态进行了量化。然而,这些方法尚未分析线粒体裂变和融合的动力学。在此,我们提出一种方法,用于测量线粒体形态,以及估计单个裂殖酵母细胞中线粒体的裂变和融合频率,这些细胞的线粒体已进行荧光标记或染色。后者依赖于在延时拍摄的每一帧中进行信号过滤后对单个线粒体进行计数。综上所述,我们提出了一种用于分析线粒体动力学的简单方案,该方案可轻松应用于其他模型系统。