Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018:1759:19-27.
doi: 10.1007/7651_2017_20.

Immunocytochemical Monitoring of PINK1/Parkin-Mediated Mitophagy in Cultured Cells

Affiliations

Immunocytochemical Monitoring of PINK1/Parkin-Mediated Mitophagy in Cultured Cells

Motoki Fujimaki et al. Methods Mol Biol. 2018.

Abstract

Both PINK1 and parkin are the responsible genes (PARK6 and PARK2, respectively) for familial early-onset Parkinson's disease (PD). Several lines of evidences have suggested that mitochondrial dysfunction would be associated with PD pathogenesis. Lewy body, one of PD pathological hallmarks, contains alpha-synuclein, a familial PD (PARK1/4)-gene product, which is eliminated by macroautophagy, while PINK1 and parkin coordinately mediate mitophagy (hereafter called as PINK1/parkin-mediated mitophagy) reported firstly by Youle's group. The mitochondrial quality control system is specific for elimination of damaged mitochondria especially in the loss of mitochondrial membrane potential induced by treatment with mitochondrial uncoupler like CCCP or FCCP. In this chapter, we summarized immunocytochemical methods to monitor the PINK1/parkin-mediated mitophagy using cultured cells.

Keywords: Familial Parkinson’s disease; Immunocytochemistry; Membrane potential; Mitochondrial uncoupler; Mitophagy; PINK1; Parkin; Parkinson’s disease.

PubMed Disclaimer

Similar articles

Cited by

Publication types

LinkOut - more resources