Cargando…
PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin
Loss-of-function mutations in PINK1 and Parkin cause parkinsonism in humans and mitochondrial dysfunction in model organisms. Parkin is selectively recruited from the cytosol to damaged mitochondria to trigger their autophagy. How Parkin recognizes damaged mitochondria, however, is unknown. Here, we...
Autores principales: | Narendra, Derek P., Jin, Seok Min, Tanaka, Atsushi, Suen, Der-Fen, Gautier, Clement A., Shen, Jie, Cookson, Mark R., Youle, Richard J. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811155/ https://www.ncbi.nlm.nih.gov/pubmed/20126261 http://dx.doi.org/10.1371/journal.pbio.1000298 |
Ejemplares similares
-
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
por: Narendra, Derek, et al.
Publicado: (2008) -
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
por: Matsuda, Noriyuki, et al.
Publicado: (2010) -
Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin
por: Tanaka, Atsushi, et al.
Publicado: (2010) -
PINK1 drives Parkin self-association and HECT-like E3 activity upstream of mitochondrial binding
por: Lazarou, Michael, et al.
Publicado: (2013) -
PINK1 and Parkin to control mitochondria remodeling
por: Koh, Hyongjong, et al.
Publicado: (2010)