Cargando…
ATP13A2 Regulates Cellular α-Synuclein Multimerization, Membrane Association, and Externalization
ATP13A2, a late endo-/lysosomal polyamine transporter, is implicated in a variety of neurodegenerative diseases, including Parkinson’s disease and Kufor–Rakeb syndrome, an early-onset atypical form of parkinsonism. Loss-of-function mutations in ATP13A2 result in lysosomal deficiency as a consequence...
Autores principales: | Si, Jianmin, Van den Haute, Chris, Lobbestael, Evy, Martin, Shaun, van Veen, Sarah, Vangheluwe, Peter, Baekelandt, Veerle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962109/ https://www.ncbi.nlm.nih.gov/pubmed/33799982 http://dx.doi.org/10.3390/ijms22052689 |
Ejemplares similares
-
Protection against Mitochondrial and Metal Toxicity Depends on Functional Lipid Binding Sites in ATP13A2
por: Martin, Shaun, et al.
Publicado: (2016) -
Pathogenic LRRK2 requires secondary factors to induce cellular toxicity
por: Lobbestael, Evy, et al.
Publicado: (2020) -
ATP13A4 Upregulation Drives the Elevated Polyamine Transport System in the Breast Cancer Cell Line MCF7
por: van Veen, Sarah, et al.
Publicado: (2023) -
ATP13A2-mediated endo-lysosomal polyamine export counters mitochondrial oxidative stress
por: Vrijsen, Stephanie, et al.
Publicado: (2020) -
ATP13A3 is a major component of the enigmatic mammalian polyamine transport system
por: Hamouda, Norin Nabil, et al.
Publicado: (2020)