Allen George F G, Toth Rachel, James John, Ganley Ian G
MRC-Protein Phosphorylation and Ubiquitylation Unit, and.
EMBO Rep. 2013 Dec;14(12):1127-35. doi: 10.1038/embor.2013.168. Epub 2013 Nov 1.
In this study, we develop a simple assay to identify mitophagy inducers on the basis of the use of fluorescently tagged mitochondria that undergo a colour change on lysosomal delivery. Using this assay, we identify iron chelators as a family of compounds that generate a strong mitophagy response. Iron chelation-induced mitophagy requires that cells undergo glycolysis, but does not require PINK1 stabilization or Parkin activation, and occurs in primary human fibroblasts as well as those isolated from a Parkinson's patient with Parkin mutations. Thus, we have identified and characterized a mitophagy pathway, the induction of which could prove beneficial as a potential therapy for several neurodegenerative diseases in which mitochondrial clearance is advantageous.
在本研究中,我们开发了一种简单的检测方法,基于使用在溶酶体递送时会发生颜色变化的荧光标记线粒体来鉴定线粒体自噬诱导剂。利用该检测方法,我们鉴定出铁螯合剂是一类能产生强烈线粒体自噬反应的化合物。铁螯合诱导的线粒体自噬要求细胞进行糖酵解,但不要求PINK1稳定化或Parkin激活,并且在原代人成纤维细胞以及从患有Parkin突变的帕金森病患者分离出的成纤维细胞中均会发生。因此,我们已经鉴定并表征了一种线粒体自噬途径,其诱导作为一种潜在治疗方法可能对几种线粒体清除有益的神经退行性疾病具有益处。