Yamashita Shun-Ichi, Kanki Tomotake
Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Methods Mol Biol. 2018;1782:315-324. doi: 10.1007/978-1-4939-7831-1_18.
Mitochondrial autophagy or mitophagy is a process that selectively degrades mitochondria via autophagy. It is believed that mitophagy degrades damaged or unnecessary mitochondria and is important for maintaining mitochondrial homeostasis. To date, it is known that several stimuli can induce mitophagy. However, some of these stimuli (including iron depletion, hypoxia, and nitrogen starvation) induce mild mitophagy, which is difficult to detect by measuring the decrease in mitochondrial mass. Recently, we have successfully detected mitophagy induced under these conditions using mito-Keima as a reporter. In this chapter, we describe the protocols for induction and detection of iron depletion- and hypoxia-induced mitophagy using the mito-Keima-expressing cells.
线粒体自噬,即线粒体选择性自噬,是一种通过自噬选择性降解线粒体的过程。人们认为线粒体自噬可降解受损或多余的线粒体,对维持线粒体稳态至关重要。迄今为止,已知有几种刺激可诱导线粒体自噬。然而,其中一些刺激(包括铁缺乏、缺氧和氮饥饿)诱导的是轻度线粒体自噬,通过测量线粒体质量的减少很难检测到。最近,我们使用线粒体靶向的红色荧光蛋白Keima作为报告基因,成功检测了在这些条件下诱导的线粒体自噬。在本章中,我们描述了使用表达线粒体靶向的红色荧光蛋白Keima的细胞诱导和检测铁缺乏及缺氧诱导的线粒体自噬的实验方案。