Esteban-Martinez L, Villarejo-Zori B, Boya P
Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Methods Enzymol. 2017;588:209-217. doi: 10.1016/bs.mie.2016.09.081. Epub 2017 Jan 3.
Mitophagy is the selective autophagic degradation of mitochondria inside lysosomes and is the only mechanism capable of eliminating whole mitochondria that are either damaged or no longer required. Mitochondrial dysfunction is a common hallmark in many pathological conditions and has been implicated in cellular damage in aged tissues. The limited availability of mitophagy research methods underscores the need for more robust, quantitative, and objective tools in order to better understand this process. Here we describe a flow cytometry-based method using MitoTracker Deep Red for mitophagy assessment that can be applied to cells and tissues. Moreover, we demonstrate that when used in conjunction with lysosomal inhibitors, our method provides a novel means of assessing mitophagic flux, which is the most reliable indicator of whether mitochondria are truly delivered to lysosomes for degradation.
线粒体自噬是溶酶体内线粒体的选择性自噬降解,是唯一能够清除受损或不再需要的整个线粒体的机制。线粒体功能障碍是许多病理状况的常见特征,并且与衰老组织中的细胞损伤有关。线粒体自噬研究方法的有限性凸显了对更强大、定量和客观工具的需求,以便更好地理解这一过程。在此,我们描述了一种基于流式细胞术的方法,该方法使用MitoTracker Deep Red进行线粒体自噬评估,可应用于细胞和组织。此外,我们证明,当与溶酶体抑制剂联合使用时,我们的方法提供了一种评估线粒体自噬通量的新方法,线粒体自噬通量是线粒体是否真正被输送到溶酶体进行降解的最可靠指标。