Vajrala Venkata Suresh, Suraniti Emmanuel, Rigoulet Michel, Devin Anne, Sojic Neso, Arbault Stéphane
Univ. Bordeaux, CNRS, ISM UMR5255, NSYSA group, ENSCBP, 33607 Pessac, France.
Integr Biol (Camb). 2016 Aug 8;8(8):836-43. doi: 10.1039/c6ib00064a. Epub 2016 Jul 7.
Microwell arrays have been developed to monitor simultaneously, and on a large scale, multiple metabolic responses of single mitochondria. Wells of 50 to 1000 μm-diameter were prepared based on easy structuration of thin polydimethylsiloxane layers (PDMS; 100 μm thickness). Their surface treatment with oxygen plasma allowed the immobilization in situ and observation with time of populations of single isolated mitochondria. Their metabolic activities could be monitored individually by fluorescence microscopy under several activation/inhibition conditions. We measured the concomitant variations of two main metabolic parameters - the endogenous NADH level and the internal membrane potential difference Δψ owing to a cationic fluorescent probe (TMRM) - at energized, uncoupled and inhibited stages of the mitochondrial respiratory chain. Microwell arrays allowed analyses on large populations, and consequently statistical studies with a single organelle resolution. Thus, we observed rapid individual polarizations and depolarizations of mitochondria following their supply with the energetic substrate, while an averaged global polarization (increase of TMRM fluorescence within mitochondria) and NADH increase were detected for the whole population. In addition, statistical correlation studies show that the NADH content of all mitochondria tends toward a metabolic limit and that their polarization-depolarization ability is ubiquitous. These results demonstrate that PDMS microwell platforms provide an innovative approach to better characterize the individual metabolic status of isolated mitochondria, possibly as a function of their cell or organ origin or in different physio-pathological situations.
微孔阵列已被开发出来,用于同时大规模监测单个线粒体的多种代谢反应。基于薄聚二甲基硅氧烷层(PDMS;厚度为100μm)易于结构化的特点,制备了直径为50至1000μm的孔。通过氧等离子体对其表面进行处理,可以原位固定单个分离的线粒体群体并随时间进行观察。在几种激活/抑制条件下,可通过荧光显微镜单独监测它们的代谢活性。我们测量了线粒体呼吸链在供能、解偶联和抑制阶段两个主要代谢参数的伴随变化——内源性NADH水平和由于阳离子荧光探针(TMRM)引起的内膜电位差Δψ。微孔阵列允许对大量群体进行分析,从而以单个细胞器分辨率进行统计研究。因此,我们观察到线粒体在供应能量底物后迅速发生个体极化和去极化,而对整个群体检测到平均的整体极化(线粒体内TMRM荧光增加)和NADH增加。此外,统计相关性研究表明,所有线粒体的NADH含量趋向于一个代谢极限,并且它们的极化-去极化能力是普遍存在的。这些结果表明,PDMS微孔平台提供了一种创新方法,能够更好地表征分离线粒体的个体代谢状态,这可能取决于它们的细胞或器官来源,或者处于不同的生理病理状况。