Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia

Mutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal dominant Parkinson disease (PD), while polymorphic LRRK2 variants are associated with sporadic PD. PD-linked mutations increase LRRK2 kinase activity and induce neurotoxicity in vitro and in vivo. The small GTPase Rab8a is a LRRK2 kin...

Descripción completa

Detalles Bibliográficos
Autores principales: Mamais, Adamantios, Kluss, Jillian H., Bonet-Ponce, Luis, Landeck, Natalie, Langston, Rebekah G., Smith, Nathan, Beilina, Alexandra, Kaganovich, Alice, Ghosh, Manik C., Pellegrini, Laura, Kumaran, Ravindran, Papazoglou, Ioannis, Heaton, George R., Bandopadhyay, Rina, Maio, Nunziata, Kim, Changyoun, LaVoie, Matthew J., Gershlick, David C., Cookson, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675653/
https://www.ncbi.nlm.nih.gov/pubmed/34914695
http://dx.doi.org/10.1371/journal.pbio.3001480

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675653/
https://www.ncbi.nlm.nih.gov/pubmed/34914695
http://dx.doi.org/10.1371/journal.pbio.3001480

Ejemplares similares