Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan.
Nat Commun. 2013;4:2428. doi: 10.1038/ncomms3428.
Eukaryotic cells maintain mitochondrial integrity through mitophagy, an autophagic process by which dysfunctional mitochondria are selectively sequestered into double-layered membrane structures, termed phagophores, and delivered to lysosomes for degradation. Here we show that small fragments of parkin-labelled mitochondria at omegasome-marked sites are engulfed by autophagic membranes one at a time. Using a light-activation scheme to impair long mitochondrial tubules, we demonstrate that sites undergoing bit-by-bit mitophagy display preferential ubiquitination, and are situated where parkin-labelled mitochondrial tubules and endoplasmic reticulum intersect. Our observations suggest contact regions between the endoplasmic reticulum and impaired mitochondria are initiation sites for local LC3 recruitment and mitochondrial remodelling that support bit-by-bit, parkin-mediated mitophagy. These results help in understanding how cells manage to fit large and morphologically heterogeneous mitochondria into micron-sized autophagic membranes during mitophagy.
真核细胞通过自噬来维持线粒体的完整性,自噬是一种选择性地将功能失调的线粒体隔离到双层膜结构中的过程,这些双层膜结构被称为吞噬体,并被递送到溶酶体中进行降解。在这里,我们表明,在 omegasome 标记的位点处,被 parkin 标记的线粒体的小片段一次一个地被自噬膜吞噬。我们使用一种光激活方案来损伤长线粒体小管,证明了正在进行逐段线粒体自噬的位点显示出优先的泛素化,并位于 parkin 标记的线粒体小管和内质网相交的地方。我们的观察结果表明,内质网和受损线粒体之间的接触区域是局部 LC3 募集和支持逐段、parkin 介导的线粒体自噬的线粒体重塑的起始位点。这些结果有助于理解细胞在进行线粒体自噬时,如何将大型和形态上异质的线粒体装配到微尺寸的自噬膜中。