Pathogenic Lysosomal Depletion in Parkinson's Disease
Biomedical Research Networking Center on Neurodegenerative Diseases · Vall d'Hebron Institut de Recerca · +3 more institutions
Abstract
Mounting evidence suggests a role for autophagy dysregulation in Parkinson's disease (PD). The bulk degradation of cytoplasmic proteins (including α-synuclein) and organelles (such as mitochondria) is mediated by macroautophagy, which involves the sequestration of cytosolic components into autophagosomes (AP) and its delivery to lysosomes. Accumulation of AP occurs in postmortem brain samples from PD patients, which has been widely attributed to an induction of autophagy. However, the cause and pathogenic significance of these changes remain unknown. Here we found in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of PD that AP accumulation and dopaminergic cell death are preceded by a marked…
Citation impact
- FWCI
- 24.67
- Percentile
- 100%
- References
- 53
Authors
7- BDBenjamin DehayCorresponding
Biomedical Research Networking Center on Neurodegenerative Diseases
- JBJordi Bové
Biomedical Research Networking Center on Neurodegenerative Diseases, Vall d'Hebron Institut de Recerca
- NRNatalia Rodríguez‐Muela
Vall d'Hebron Institut de Recerca, National Research Council, Centro de Investigaciones Biológicas Margarita Salas
- CPCéline Perier
Biomedical Research Networking Center on Neurodegenerative Diseases, Vall d'Hebron Institut de Recerca
- ARAriadna Recasens
Biomedical Research Networking Center on Neurodegenerative Diseases, Vall d'Hebron Institut de Recerca
Topics & keywords
- Autophagy
- TFEB
- Neurodegeneration
- Cell biology
- Programmed cell death
- Lysosome
- Biology
- Cytosol