Niemann-Pick Disease Type C (NPDC) by Mutation of

Niemann-Pick disease type C cholesterol trafficking lysosomal proteins lysosomal storage disorders oxidative stress

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
21 Nov 2023
Historique:
received: 24 10 2023
revised: 13 11 2023
accepted: 17 11 2023
medline: 23 12 2023
pubmed: 23 12 2023
entrez: 23 12 2023
Statut: epublish

Résumé

Cholesterol trafficking is initiated by the endocytic pathway and transported from endo/lysosomes to other intracellular organelles. Deficiencies in cholesterol-sensing and binding proteins NPC1 and NPC2 induce accumulation in lysosomes and the malfunction of trafficking to other organelles. Each organelle possesses regulatory factors to induce cholesterol trafficking. The mutation of

Identifiants

pubmed: 38136141
pii: antiox12122021
doi: 10.3390/antiox12122021
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : National Research Foundation of Korea (NRF) grant funded by the Korean government
ID : 2022R1A2C1003890 (JHH)

Auteurs

Dongun Lee (D)

Department of Health Sciences & Technology, GAIHST, Gachon University, 155 Getbeolro, Yeonsu-gu, Incheon 21999, Republic of Korea.

Jeong Hee Hong (JH)

Department of Health Sciences & Technology, GAIHST, Gachon University, 155 Getbeolro, Yeonsu-gu, Incheon 21999, Republic of Korea.

Classifications MeSH