dc.contributor.author
Lu, Albert
dc.date.issued
2024-10-18T13:19:11Z
dc.date.issued
2024-10-18T13:19:11Z
dc.date.issued
2022-10-01
dc.date.issued
2024-10-18T13:19:11Z
dc.identifier
https://hdl.handle.net/2445/215878
dc.description.abstract
NPC1 plays a central role in cholesterol egress from endolysosomes, a critical step for maintaining intracellular cholesterol homeostasis. Despite recent advances in the field, the full repertoire of molecules and pathways involved in this process remains unknown. Emerging evidence suggests the existence of NPC1-independent, alternative routes. These may involve vesicular and non-vesicular mechanisms, as well as release of extracellular vesicles. Understanding the underlying molecular mechanisms that bypass NPC1 function could have important implications for the development of therapies for lysosomal storage disorders. Here we discuss how cholesterol may be exported from lysosomes in which NPC1 function is impaired.
dc.format
application/pdf
dc.relation
Reproducció del document publicat a: https://doi.org/10.1002/bies.202200111
dc.relation
BioEssays, 2022, vol. 44, num.10, p. 1-12
dc.relation
https://doi.org/10.1002/bies.202200111
dc.rights
cc-by.nc (c) Lu, 2022
dc.rights
http://creativecommons.org/licenses/by-nc/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biomedicina)
dc.subject
Glicoproteïnes
dc.title
Endolysosomal cholesterol export: More than just NPC1
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion