TMEM175 : A lysosomal ion channel associated with neurological diseases

Copyright © 2023. Published by Elsevier Inc..

Lysosomes are acidic intracellular organelles with autophagic functions that are critical for protein degradation and mitochondrial homeostasis, while abnormalities in lysosomal physiological functions are closely associated with neurological disorders. Transmembrane protein 175 (TMEM175), an ion channel in the lysosomal membrane that is essential for maintaining lysosomal acidity, has been proven to coordinate with V-ATPase to modulate the luminal pH of the lysosome to assist the digestion of abnormal proteins and organelles. However, there is considerable controversy about the characteristics of TMEM175. In this review, we introduce the research progress on the structural, modulatory, and functional properties of TMEM175, followed by evidence of its relevance for neurological disorders. Finally, we discuss the potential value of TMEM175 as a therapeutic target in the hope of providing new directions for the treatment of neurodegenerative diseases.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:185

Enthalten in:

Neurobiology of disease - 185(2023) vom: 13. Sept., Seite 106244

Sprache:

Englisch

Beteiligte Personen:

Wu, Luojia [VerfasserIn]
Lin, Yue [VerfasserIn]
Song, Jiali [VerfasserIn]
Li, Longshan [VerfasserIn]
Rao, Xiuqin [VerfasserIn]
Wan, Wei [VerfasserIn]
Wei, Gen [VerfasserIn]
Hua, Fuzhou [VerfasserIn]
Ying, Jun [VerfasserIn]

Links:

Volltext

Themen:

Autophagy
Ion Channels
Ion channel
Journal Article
Lysosomal membrane protein
Lysosome
Neurological disease
Potassium Channels
Research Support, Non-U.S. Gov't
Review
TMEM175
TMEM175 protein, human

Anmerkungen:

Date Completed 04.09.2023

Date Revised 02.10.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.nbd.2023.106244

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM360240380