Specifc phospholipids regulate the acquisition of neuronal and astroglial identities in post-mitotic cells

Hitherto, the known mechanisms underpinning cell-fate specifcation act on neural progenitors, afecting their commitment to generate neuron or glial cells. Here, we show that particular phospholipids supplemented in the culture media modify the commitment of post-mitotic neural cells in vitro. Pho...

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Detalles Bibliográficos
Autores principales: Montaner, Aneley Natalia, Da Silva Santana, Themis Taynah, Schroeder, Timm, Einicker-Lamas, Marcelo, Girardini, Javier, Romualdo Costa, Marcos, Banchio, Claudia
Formato: article artículo publishedVersion
Lenguaje:Inglés
Publicado: Nature 2021
Materias:
Specific Phospholipids
Neuronal Identity
Astrocyte Identity
Neuroglia
Post-Mitotic Cells
Acceso en línea:http://hdl.handle.net/2133/19682
http://hdl.handle.net/2133/19682
Aporte de:
Repositorio Hipermedial de la Universidad Nacional de Rosario (UNR) de Universidad Nacional de Rosario
Descripción
Sumario:Hitherto, the known mechanisms underpinning cell-fate specifcation act on neural progenitors, afecting their commitment to generate neuron or glial cells. Here, we show that particular phospholipids supplemented in the culture media modify the commitment of post-mitotic neural cells in vitro. Phosphatidylcholine (PtdCho)-enriched media enhances neuronal diferentiation at the expense of astroglial and unspecifed cells. Conversely, phosphatidylethanolamine (PtdEtn) enhances astroglial diferentiation and accelerates astrocyte maturation. The ability of phospholipids to modify the fate of post-mitotic cells depends on its presence during a narrow time-window during cell diferentiation and it is mediated by the selective activation of particular signaling pathways. While PtdCho-mediated efect on neuronal diferentiation depends on cAMP-dependent kinase (PKA)/calcium responsive element binding protein (CREB), PtdEtn stimulates astrogliogenesis through the activation of the MEK/ ERK signaling pathway. Collectively, our results provide an additional degree of plasticity in neural cell specifcation and further support the notion that cell diferentiation is a reversible phenomenon. They also contribute to our understanding of neuronal and glial lineage specifcation in the central nervous system, opening up new avenues to retrieve neurogenic capacity in the brain.

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