Cargando…
The lysosomal protein cathepsin L is a progranulin protease
Haploinsufficiency of GRN, the gene encoding progranulin (PGRN), causes frontotemporal lobar degeneration (FTLD), the second most common cause of early-onset dementia. Receptor-mediated lysosomal targeting has been shown to regulate brain PGRN levels, and complete deficiency of PGRN is a direct caus...
Autores principales: | Lee, Chris W., Stankowski, Jeannette N., Chew, Jeannie, Cook, Casey N., Lam, Ying-Wai, Almeida, Sandra, Carlomagno, Yari, Lau, Kwok-Fai, Prudencio, Mercedes, Gao, Fen-Biao, Bogyo, Matthew, Dickson, Dennis W., Petrucelli, Leonard |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526245/ https://www.ncbi.nlm.nih.gov/pubmed/28743268 http://dx.doi.org/10.1186/s13024-017-0196-6 |
Ejemplares similares
-
Acetylation: a new key to unlock tau’s role in neurodegeneration
por: Cook, Casey, et al.
Publicado: (2014) -
Targeted manipulation of the sortilin–progranulin axis rescues progranulin haploinsufficiency
por: Lee, Wing C., et al.
Publicado: (2014) -
Loss of Progranulin Results in Increased Pan-Cathepsin Activity and Reduced LAMP1 Lysosomal Protein
por: Anderson, Abigail, et al.
Publicado: (2023) -
Lysosomal processing of progranulin
por: Zhou, Xiaolai, et al.
Publicado: (2017) -
Processing of progranulin into granulins involves multiple lysosomal proteases and is affected in frontotemporal lobar degeneration
por: Mohan, Swetha, et al.
Publicado: (2021)