Pregled bibliografske jedinice broj: 1175147
Impaired Retromer Function in Niemann-Pick Type C Disease Is Dependent on Intracellular Cholesterol Accumulation
Impaired Retromer Function in Niemann-Pick Type C Disease Is Dependent on Intracellular Cholesterol Accumulation // International journal of molecular sciences, 22 (2021), 24; 13256, 27 doi:10.3390/ijms222413256 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1175147 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Impaired Retromer Function in Niemann-Pick Type C Disease Is Dependent on Intracellular Cholesterol Accumulation
Autori
Dominko, Kristina ; Rastija, Ana ; Sobočanec, Sandra ; Vidatić, Lea ; Meglaj, Sarah ; Lovinčić Babić, Andrea ; Hutter-Paier, Birgit ; Colombo, Alessio-Vittorio, ; Lichtenthaler, Stefan F. ; Tahirović, Sabina ; Hećimović, Silva
Izvornik
International journal of molecular sciences (1422-0067) 22
(2021), 24;
13256, 27
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
cholesterol homeostasis ; endolysosomal pathway ; neurodegeneration ; neurodegenerative diseases ; NPC1 ; rare diseases ; retromer
Sažetak
Niemann-Pick type C disease (NPC) is a rare inherited neurodegenerative disorder characterized by an accumulation of intracellular cholesterol within late endosomes and lysosomes due to NPC1 or NPC2 dysfunction. In this work, we tested the hypothesis that retromer impairment may be involved in the pathogenesis of NPC and may contribute to increased amyloidogenic processing of APP and enhanced BACE1-mediated proteolysis observed in NPC disease. Using NPC1-null cells, primary mouse NPC1-deficient neurons and NPC1-deficient mice (BALB/cNctr-Npc1m1N), we show that retromer function is impaired in NPC. This is manifested by altered transport of the retromer core components Vps26, Vps35 and/or retromer receptor sorLA and by retromer accumulation in neuronal processes, such as within axonal swellings. Changes in retromer distribution in NPC1 mouse brains were observed already at the presymptomatic stage (at 4-weeks of age), indicating that the retromer defect occurs early in the course of NPC disease and may contribute to downstream pathological processes. Furthermore, we show that cholesterol depletion in NPC1-null cells and in NPC1 mouse brains reverts retromer dysfunction, suggesting that retromer impairment in NPC is mechanistically dependent on cholesterol accumulation. Thus, we characterized retromer dysfunction in NPC and propose that the rescue of retromer impairment may represent a novel therapeutic approach against NPC.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
HRZZ-IP-2016-06-2799 - Molekularni mehanizam neurodegeneracije u Niemann-Pickovoj bolesti tip C (neuroNiPiC) (Katušić Hećimović, Silva, HRZZ - 2016-06) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Kristina Dominko
(autor)
Sandra Sobočanec
(autor)
Ana Rastija
(autor)
Silva Katušić Hećimović
(autor)
Sarah Meglaj
(autor)
Lea Vidatić
(autor)
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi www.mdpi.com doi.org fulir.irb.hrCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE