Cargando…
Astrocytes expressing mutant SOD1 and TDP43 trigger motoneuron death that is mediated via sodium channels and nitroxidative stress
Amyotrophic lateral sclerosis (ALS) is a fatal paralytic disorder caused by dysfunction and degeneration of motor neurons. Multiple disease-causing mutations, including in the genes for SOD1 and TDP-43, have been identified in ALS. Astrocytes expressing mutant SOD1 are strongly implicated in the pat...
Autores principales: | Rojas, Fabiola, Cortes, Nicole, Abarzua, Sebastian, Dyrda, Agnieszka, van Zundert, Brigitte |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916762/ https://www.ncbi.nlm.nih.gov/pubmed/24570655 http://dx.doi.org/10.3389/fncel.2014.00024 |
Ejemplares similares
-
Mature iPSC-derived astrocytes of an ALS/FTD patient carrying the TDP43(
A90V
) mutation display a mild reactive state and release polyP toxic to motoneurons
por: Rojas, Fabiola, et al.
Publicado: (2023) -
Reactive oxygen species trigger motoneuron death in non-cell-autonomous models of ALS through activation of c-Abl signaling
por: Rojas, Fabiola, et al.
Publicado: (2015) -
Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusions
por: Farrawell, Natalie E., et al.
Publicado: (2015) -
Augmentation of spinal cord glutamatergic synaptic currents in zebrafish primary motoneurons expressing mutant human TARDBP (TDP-43)
por: Petel Légaré, Virginie, et al.
Publicado: (2019) -
Disulfide cross-linked multimers of TDP-43 and spinal motoneuron loss in a TDP-43(A315T) ALS/FTD mouse model
por: Bargsted, Leslie, et al.
Publicado: (2017)