Center for Cell Death, Injury & Regeneration, Medical University of South Carolina, QF308 Quadrangle Bldg., 280 Calhoun St., P. O Box 250140, Charleston, SC 29425, USA.
Am J Physiol Cell Physiol. 2011 Feb;300(2):C308-17. doi: 10.1152/ajpcell.00056.2010. Epub 2010 Nov 24.
Fasting in vivo and nutrient deprivation in vitro enhance sequestration of mitochondria and other organelles by autophagy for recycling of essential nutrients. Here our goal was to use a transgenic mouse strain expressing green fluorescent protein (GFP) fused to rat microtubule-associated protein-1 light chain 3 (LC3), a marker protein for autophagy, to characterize the dynamics of mitochondrial turnover by autophagy (mitophagy) in hepatocytes during nutrient deprivation. In complete growth medium, GFP-LC3 fluorescence was distributed diffusely in the cytosol and incorporated in mostly small (0.2-0.3 μm) patches in proximity to mitochondria, which likely represent preautophagic structures (PAS). After nutrient deprivation plus 1 μM glucagon to simulate fasting, PAS grew into green cups (phagophores) and then rings (autophagosomes) that enveloped individual mitochondria, a process that was blocked by 3-methyladenine. Autophagic sequestration of mitochondria took place in 6.5 ± 0.4 min and often occurred coordinately with mitochondrial fission. After ring formation and apparent sequestration, mitochondria depolarized in 11.8 ± 1.4 min, as indicated by loss of tetramethylrhodamine methylester fluorescence. After ring formation, LysoTracker Red uptake, a marker of acidification, occurred gradually, becoming fully evident at 9.9 ± 1.9 min of ring formation. After acidification, GFP-LC3 fluorescence dispersed. PicoGreen labeling of mitochondrial DNA (mtDNA) showed that mtDNA was also sequestered and degraded in autophagosomes. Overall, the results indicate that PAS serve as nucleation sites for mitophagy in hepatocytes during nutrient deprivation. After autophagosome formation, mitochondrial depolarization and vesicular acidification occur, and mitochondrial contents, including mtDNA, are degraded.
在体内禁食和体外营养缺乏的情况下,自噬会增强对线粒体和其他细胞器的隔离,以回收必需的营养物质。在这里,我们的目标是使用一种表达绿色荧光蛋白(GFP)与大鼠微管相关蛋白-1 轻链 3(LC3)融合的转基因小鼠品系,LC3 是自噬的标记蛋白,来描述营养缺乏期间肝细胞中线粒体自噬(mitophagy)的线粒体周转率的动态变化。在完全生长培养基中,GFP-LC3 荧光弥散分布在细胞质中,并整合到靠近线粒体的大多数小(0.2-0.3μm)斑点中,这些斑点可能代表自噬前体结构(PAS)。在营养缺乏加 1μM 胰高血糖素模拟禁食后,PAS 生长成绿色杯子(吞噬体),然后是环(自噬体),这些环包裹单个线粒体,这个过程被 3-甲基腺嘌呤阻断。线粒体的自噬隔离发生在 6.5±0.4 分钟内,并且经常与线粒体裂变协调发生。在环形成和明显隔离后,线粒体在 11.8±1.4 分钟内去极化,如四甲基罗丹明甲酯荧光的丧失所表明的。在环形成后,溶酶体追踪器红色摄取(酸化的标志物)逐渐发生,在环形成的 9.9±1.9 分钟时完全明显。在酸化后,GFP-LC3 荧光分散。线粒体 DNA(mtDNA)的 PicoGreen 标记表明 mtDNA 也在线粒体自噬体中被隔离和降解。总的来说,这些结果表明在营养缺乏期间,PAS 作为肝细胞中线粒体自噬的成核位点。在自噬体形成后,线粒体去极化和囊泡酸化发生,线粒体内容物,包括 mtDNA,被降解。