Ageing, cellular senescence and neurodegenerative disease

M Kritsilis, S V. Rizou, PN Koutsoudaki… - International journal of …, 2018 - mdpi.com
Ageing is a major risk factor for develo** many neurodegenerative diseases. Cellular
senescence is a homeostatic biological process that has a key role in driving ageing. There …

Cellular senescence in neurodegenerative diseases

C Martínez-Cué, N Rueda - Frontiers in cellular neuroscience, 2020 - frontiersin.org
Cellular senescence is a homeostatic biological process characterized by a permanent state
of cell cycle arrest that can contribute to the decline of the regenerative potential and …

Glucocerebrosidase and its relevance to Parkinson disease

J Do, C McKinney, P Sharma, E Sidransky - Molecular neurodegeneration, 2019 - Springer
Mutations in GBA1, the gene encoding the lysosomal enzyme glucocerebrosidase, are
among the most common known genetic risk factors for the development of Parkinson …

Reactive oxygen species as a link between antioxidant pathways and autophagy

D Li, Z Ding, K Du, X Ye… - Oxidative Medicine and …, 2021 - Wiley Online Library
Reactive oxygen species (ROS) are highly reactive molecules that can oxidize proteins,
lipids, and DNA. Under physiological conditions, ROS are mainly generated in the …

Neuronal soma-derived degradative lysosomes are continuously delivered to distal axons to maintain local degradation capacity

T Farfel-Becker, JC Roney, XT Cheng, S Li, SR Cuddy… - Cell reports, 2019 - cell.com
Neurons face the challenge of maintaining cellular homeostasis through lysosomal
degradation. While enzymatically active degradative lysosomes are enriched in the soma …

Lipids at the crossroad of α-synuclein function and dysfunction: biological and pathological implications

NP Alza, PA Iglesias González, MA Conde… - Frontiers in Cellular …, 2019 - frontiersin.org
Since its discovery, the study of the biological role of α-synuclein and its pathological
implications has been the subject of increasing interest. The propensity to adopt different …

Pathological α-syn aggregation is mediated by glycosphingolipid chain length and the physiological state of α-syn in vivo

K Fredriksen, S Aivazidis, K Sharma… - Proceedings of the …, 2021 - National Acad Sciences
GBA1 mutations that encode lysosomal β-glucocerebrosidase (GCase) cause the lysosomal
storage disorder Gaucher disease (GD) and are strong risk factors for synucleinopathies …

TFEB biology and agonists at a glance

M Chen, Y Dai, S Liu, Y Fan, Z Ding, D Li - Cells, 2021 - mdpi.com
Autophagy is a critical regulator of cellular survival, differentiation, development, and
homeostasis, dysregulation of which is associated with diverse diseases including cancer …

Clinical, mechanistic, biomarker, and therapeutic advances in GBA1-associated Parkinson's disease

X Zhang, H Wu, B Tang, J Guo - Translational Neurodegeneration, 2024 - Springer
Parkinson's disease (PD) is the second most common neurodegenerative disease. The
development of PD is closely linked to genetic and environmental factors, with GBA1 …

GBA1 inactivation in oligodendrocytes affects myelination and induces neurodegenerative hallmarks and lipid dyshomeostasis in mice

I Gregorio, L Russo, E Torretta, P Barbacini… - Molecular …, 2024 - Springer
Background Mutations in the β-glucocerebrosidase (GBA1) gene do cause the lysosomal
storage Gaucher disease (GD) and are among the most frequent genetic risk factors for …