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Título

Axonal and Myelin Neuroprotection by the Peptoid BN201 in Brain Inflammation

AutorVilloslada, Pablo; Vila, Gemma; Colafrancesco, Valeria; Moreno, Beatriz; Fernández-Diez, Begoña; Vazquez, R; Pertsovskaya, Inna; Zubizarreta, Irati; Pulido-Valdeolivas, Irene; Messeguer, Joaquim CSIC; Vendrell-Navarro, Gloria; Frade López, José María CSIC ORCID ; López-Sánchez, Noelia CSIC ORCID; Teixidó, Meritxell; Giralt, Ernest; Masso, Mar; Dugas, Jason C.; Leonoudakis, Dmitri; Lariosa-Willingham, Karen D.; Steinman, Lawrence; Messeguer, Àngel
Palabras claveNeuroprotection
glaucoma
Multiple sclerosis
Neurodegenerative diseases
Neuroinflammation
Fecha de publicación2019
EditorSpringer Nature
CitaciónNeurotherapeutics 16: 808- 827 (2019)
ResumenThe development of neuroprotective therapies is a sought-after goal. By screening combinatorial chemical libraries using in vitro assays, we identified the small molecule BN201 that promotes the survival of cultured neural cells when subjected to oxidative stress or when deprived of trophic factors. Moreover, BN201 promotes neuronal differentiation, the differentiation of precursor cells to mature oligodendrocytes in vitro, and the myelination of new axons. BN201 modulates several kinases participating in the insulin growth factor 1 pathway including serum-glucocorticoid kinase and midkine, inducing the phosphorylation of NDRG1 and the translocation of the transcription factor Foxo3 to the cytoplasm. In vivo, BN201 prevents axonal and neuronal loss, and it promotes remyelination in models of multiple sclerosis, chemically induced demyelination, and glaucoma. In summary, we provide a new promising strategy to promote neuroaxonal survival and remyelination, potentially preventing disability in brain diseases.
Versión del editorhttp://dx.doi.org/10.1007/s13311-019-00717-4
URIhttp://hdl.handle.net/10261/203085
DOI10.1007/s13311-019-00717-4
Identificadoresdoi: 10.1007/s13311-019-00717-4
issn: 1878-7479
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