Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia

Niemann-Pick type C disease is a rare childhood neurodegenerative disorder predominantly caused by mutations in NPC1, resulting in abnormal late endosomal and lysosomal defects. Here the authors show that NPC1 disruption largely impairs microglial function.

Guardado en:
Detalles Bibliográficos
Autores principales: Alessio Colombo, Lina Dinkel, Stephan A. Müller, Laura Sebastian Monasor, Martina Schifferer, Ludovico Cantuti-Castelvetri, Jasmin König, Lea Vidatic, Tatiana Bremova-Ertl, Andrew P. Lieberman, Silva Hecimovic, Mikael Simons, Stefan F. Lichtenthaler, Michael Strupp, Susanne A. Schneider, Sabina Tahirovic
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/086477f8dbac4c818ed45236ab495029
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:086477f8dbac4c818ed45236ab495029
record_format dspace
spelling oai:doaj.org-article:086477f8dbac4c818ed45236ab4950292021-12-02T13:14:59ZLoss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia10.1038/s41467-021-21428-52041-1723https://doaj.org/article/086477f8dbac4c818ed45236ab4950292021-02-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-21428-5https://doaj.org/toc/2041-1723Niemann-Pick type C disease is a rare childhood neurodegenerative disorder predominantly caused by mutations in NPC1, resulting in abnormal late endosomal and lysosomal defects. Here the authors show that NPC1 disruption largely impairs microglial function.Alessio ColomboLina DinkelStephan A. MüllerLaura Sebastian MonasorMartina SchiffererLudovico Cantuti-CastelvetriJasmin KönigLea VidaticTatiana Bremova-ErtlAndrew P. LiebermanSilva HecimovicMikael SimonsStefan F. LichtenthalerMichael StruppSusanne A. SchneiderSabina TahirovicNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-20 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Alessio Colombo
Lina Dinkel
Stephan A. Müller
Laura Sebastian Monasor
Martina Schifferer
Ludovico Cantuti-Castelvetri
Jasmin König
Lea Vidatic
Tatiana Bremova-Ertl
Andrew P. Lieberman
Silva Hecimovic
Mikael Simons
Stefan F. Lichtenthaler
Michael Strupp
Susanne A. Schneider
Sabina Tahirovic
Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
description Niemann-Pick type C disease is a rare childhood neurodegenerative disorder predominantly caused by mutations in NPC1, resulting in abnormal late endosomal and lysosomal defects. Here the authors show that NPC1 disruption largely impairs microglial function.
format article
author Alessio Colombo
Lina Dinkel
Stephan A. Müller
Laura Sebastian Monasor
Martina Schifferer
Ludovico Cantuti-Castelvetri
Jasmin König
Lea Vidatic
Tatiana Bremova-Ertl
Andrew P. Lieberman
Silva Hecimovic
Mikael Simons
Stefan F. Lichtenthaler
Michael Strupp
Susanne A. Schneider
Sabina Tahirovic
author_facet Alessio Colombo
Lina Dinkel
Stephan A. Müller
Laura Sebastian Monasor
Martina Schifferer
Ludovico Cantuti-Castelvetri
Jasmin König
Lea Vidatic
Tatiana Bremova-Ertl
Andrew P. Lieberman
Silva Hecimovic
Mikael Simons
Stefan F. Lichtenthaler
Michael Strupp
Susanne A. Schneider
Sabina Tahirovic
author_sort Alessio Colombo
title Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
title_short Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
title_full Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
title_fullStr Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
title_full_unstemmed Loss of NPC1 enhances phagocytic uptake and impairs lipid trafficking in microglia
title_sort loss of npc1 enhances phagocytic uptake and impairs lipid trafficking in microglia
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/086477f8dbac4c818ed45236ab495029
work_keys_str_mv AT alessiocolombo lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT linadinkel lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT stephanamuller lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT laurasebastianmonasor lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT martinaschifferer lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT ludovicocantuticastelvetri lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT jasminkonig lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT leavidatic lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT tatianabremovaertl lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT andrewplieberman lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT silvahecimovic lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT mikaelsimons lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT stefanflichtenthaler lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT michaelstrupp lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT susanneaschneider lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
AT sabinatahirovic lossofnpc1enhancesphagocyticuptakeandimpairslipidtraffickinginmicroglia
_version_ 1718393370731085824