Defective lysosomal acidification: a new prognostic marker and therapeutic target for neurodegenerative diseases

CH Lo, J Zeng - Translational Neurodegeneration, 2023 - Springer
Lysosomal acidification dysfunction has been implicated as a key driving factor in the
pathogenesis of neurodegenerative diseases, including Alzheimer's disease and …

The aging lysosome: An essential catalyst for late-onset neurodegenerative diseases

RA Nixon - Biochimica et Biophysica Acta (BBA)-Proteins and …, 2020 - Elsevier
Lysosomes figure prominently in theories of aging as the proteolytic system most
responsible for eliminating growing burdens of damaged proteins and organelles in aging …

Lysosome trafficking and signaling in health and neurodegenerative diseases

PPY Lie, RA Nixon - Neurobiology of disease, 2019 - Elsevier
Lysosomes, single-membrane organelles defined by a uniquely strong acidic lumenal pH
and high content of acid hydrolases, are the shared degradative compartments of the …

Lysosomal dysfunction in neurodegeneration: emerging concepts and methods

V Udayar, Y Chen, E Sidransky, R Jagasia - Trends in neurosciences, 2022 - cell.com
The understanding of lysosomes has come a long way since the initial discovery of their role
in degrading cellular waste. The lysosome is now recognized as a highly dynamic organelle …

[HTML][HTML] Preserving lysosomal function in the aging brain: insights from neurodegeneration

W Peng, G Minakaki, M Nguyen, D Krainc - Neurotherapeutics, 2019 - Elsevier
Lysosomes are acidic, membrane-bound organelles that serve as the primary catabolic
compartment of the cell. They are crucial to a variety of cellular processes from nutrient …

Lysosomes as a therapeutic target

SR Bonam, F Wang, S Muller - Nature reviews Drug discovery, 2019 - nature.com
Lysosomes are membrane-bound organelles with roles in processes involved in degrading
and recycling cellular waste, cellular signalling and energy metabolism. Defects in genes …

The rapidly evolving view of lysosomal storage diseases

G Parenti, DL Medina, A Ballabio - EMBO molecular medicine, 2021 - embopress.org
Lysosomal storage diseases are a group of metabolic disorders caused by deficiencies of
several components of lysosomal function. Most commonly affected are lysosomal …

Lysosomal function and dysfunction: mechanism and disease

P Boya - Antioxidants & redox signaling, 2012 - liebertpub.com
Significance: Lysosomes are organelles in which cellular degradation occurs in a controlled
manner, separated from other cellular components. As several pathways terminate in the …

Lysosomal acidification dysfunction in microglia: an emerging pathogenic mechanism of neuroinflammation and neurodegeneration

JD Quick, C Silva, JH Wong, KL Lim… - Journal of …, 2023 - Springer
Microglia are the resident innate immune cells in the brain with a major role in orchestrating
immune responses. They also provide a frontline of host defense in the central nervous …

Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology

C Settembre, RM Perera - Nature Reviews Molecular Cell Biology, 2024 - nature.com
Every cell must satisfy basic requirements for nutrient sensing, utilization and recycling
through macromolecular breakdown to coordinate programmes for growth, repair and stress …