Lysosomes as dynamic regulators of cell and organismal homeostasis

A Ballabio, JS Bonifacino - Nature reviews Molecular cell biology, 2020 - nature.com
Exciting new discoveries have transformed the view of the lysosome from a static organelle
dedicated to the disposal and recycling of cellular waste to a highly dynamic structure that …

Programmed cell death in spinal cord injury pathogenesis and therapy

Z Shi, S Yuan, L Shi, J Li, G Ning, X Kong… - Cell …, 2021 - Wiley Online Library
Spinal cord injury (SCI) always leads to functional deterioration due to a series of processes
including cell death. In recent years, programmed cell death (PCD) is considered to be a …

[HTML][HTML] Autophagy in neurodegenerative diseases: from mechanism to therapeutic approach

J Nah, J Yuan, YK Jung - Molecules and cells, 2015 - Elsevier
Autophagy is a lysosome-dependent intracellular degradation process that allows recycling
of cytoplasmic constituents into bioenergetic and biosynthetic materials for maintenance of …

SOD1 function and its implications for amyotrophic lateral sclerosis pathology: new and renascent themes

RKA Bunton-Stasyshyn, RA Saccon… - The …, 2015 - journals.sagepub.com
The canonical role of superoxide dismutase 1 (SOD1) is as an antioxidant enzyme
protecting the cell from reactive oxygen species toxicity. SOD1 was also the first gene in …

[HTML][HTML] Resveratrol improves motoneuron function and extends survival in SOD1G93A ALS mice

R Mancuso, J Del Valle, L Modol, A Martinez… - …, 2014 - Elsevier
Amyotrophic lateral sclerosis (ALS) is an adult onset neurodegenerative disease that causes
progressive paralysis and death due to degeneration of motoneurons in spinal cord …

Brain disorders due to lysosomal dysfunction

A Fraldi, AD Klein, DL Medina… - Annual review of …, 2016 - annualreviews.org
Recent studies of autophagic and lysosomal pathways have significantly changed our
understanding of lysosomes; once thought to be simple degradative and recycling centers …

SQSTM1 mutations–bridging Paget disease of bone and ALS/FTLD

SL Rea, V Majcher, MS Searle, R Layfield - Experimental cell research, 2014 - Elsevier
Paget disease of bone (PDB) is a skeletal disorder common in Western Europe but
extremely rare in the Indian subcontinent and Far East. The condition has a strong genetic …

[HTML][HTML] Mitochondria: a Promising Convergent Target for the treatment of amyotrophic lateral sclerosis

T Cunha-Oliveira, L Montezinho, RF Simões… - Cells, 2024 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease
characterized by the progressive loss of motor neurons, for which current treatment options …

[HTML][HTML] Protein aggregation and dysfunction of autophagy-lysosomal pathway: a vicious cycle in lysosomal storage diseases

A Monaco, A Fraldi - Frontiers in Molecular Neuroscience, 2020 - frontiersin.org
Many neurodegenerative conditions are characterized by the deposition of protein
aggregates (mainly amyloid-like) in the central nervous system (CNS). In post-mitotic CNS …

Mitophagy in neurodegenerative diseases

C Rodolfo, S Campello, F Cecconi - Neurochemistry international, 2018 - Elsevier
Neurodegenerative diseases, such as Parkinson's disease (PD), Alzheimer's disease (AD),
Huntington's disease (HD), and Amyotrophic Lateral Sclerosis (ALS), are a complex “family” …