In Vitro Effects of Methylprednisolone over Oligodendroglial Cells: Foresight to Future Cell Therapies

The implantation of oligodendrocyte precursor cells may be a useful therapeutic strategy for targeting remyelination. However, it is yet to be established how these cells behave after implantation and whether they retain the capacity to proliferate or differentiate into myelin-forming oligodendrocyt...

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Detalles Bibliográficos
Autores: Gómez Pinedo, Ulises, Matias-Guiu Antem, Jordi, Ojeda Hernández, Doddy Denise, Fuente Martín, Sarah De La, Mohammed-Fathy Kamal, Ola, Benito Martín, María Soledad, Selma Calvo, Belén, Montero Escribano, Paloma, Matías-Guiu Guía, Jorge
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/104914
Acceso en línea:https://hdl.handle.net/20.500.14352/104914
Access Level:acceso abierto
Palabra clave:61
Multiple sclerosis
HOG cells
oligodendrocyte precursor cells
oligodendrocytes
corticosteroids
demyelination
remyelination
Ciencias Biomédicas
32 Ciencias Médicas
Descripción
Sumario:The implantation of oligodendrocyte precursor cells may be a useful therapeutic strategy for targeting remyelination. However, it is yet to be established how these cells behave after implantation and whether they retain the capacity to proliferate or differentiate into myelin-forming oligodendrocytes. One essential issue is the creation of administration protocols and determining which factors need to be well established. There is controversy around whether these cells may be implanted simultaneously with corticosteroid treatment, which is widely used in many clinical situations. This study assesses the influence of corticosteroids on the capacity for proliferation and differentiation and the survival of human oligodendroglioma cells. Our findings show that corticosteroids reduce the capacity of these cells to proliferate and to differentiate into oligodendrocytes and decrease cell survival. Thus, their effect does not favour remyelination; this is consistent with the results of studies with rodent cells. In conclusion, protocols for the administration of oligodendrocyte lineage cells with the aim of repopulating oligodendroglial niches or repairing demyelinated axons should not include corticosteroids, given the evidence that the effects of these drugs may undermine the objectives of cell transplantation.