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The ubiquitin kinase-ligase pair PINK1-PRKN identifies and selectively marks damaged mitochondria for elimination via the autophagy-lysosome system (mitophagy). While this cytoprotective pathway has been extensively studied in vitro upon acute and complete depolarization of mitochondria, the significance of PINK1-PRKN mitophagy in vivo is less well established. Here we used a novel approach to study PINK1-PRKN signaling in different energetically demanding tissues of mice during normal aging. We demonstrate a generally increased expression of both genes and enhanced enzymatic activity with aging across tissue types. Collectively our data suggest a distinct regulation of PINK1-PRKN signaling under basal conditions with the most pronounced activation and flux of the pathway in mouse heart compared to brain or skeletal muscle. Our biochemical analyses complement existing mitophagy reporter readouts and provide an important baseline assessment in vivo, setting the stage for further investigations of the PINK1-PRKN pathway during stress and in relevant disease conditions.Abbreviations: ECL: electrochemiluminescence; ELISA: enzyme-linked immunosorbent assay; MSD: Meso Scale Discovery; PD: Parkinson disease; p-S65-Ub: Serine-65 phosphorylated ubiquitin; RT-PCR: real-time polymerase chain reaction; Ub: ubiquitin; WT: wild-type.
Baninameh et al. (Sat,) studied this question.