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  Peripheral nervous system progenitors can be reprogrammed to produce myelinating oligodendrocytes and repair brain lesions

Binder, E., Rukavina, M., Hassani, H., Weber, M., Nakatani, H., Reiff, T., et al. (2011). Peripheral nervous system progenitors can be reprogrammed to produce myelinating oligodendrocytes and repair brain lesions. The Journal of Neuroscience, 31(17), 6379-6391.

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Binder, E.1, Autor           
Rukavina, M., Autor
Hassani, H., Autor
Weber, M.2, Autor           
Nakatani, H., Autor
Reiff, T.1, Autor           
Parras, C., Autor
Taylor, V., Autor
Rohrer, H.2, Autor           
Affiliations:
1Neurochemistry Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461704              
2Developmental Neurobiology Group, Max Planck Institute for Brain Research, Max Planck Society, ou_2461697              

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 Zusammenfassung: Neural crest stem cells (NCSCs) give rise to the neurons and glia of the peripheral nervous system (PNS). NCSC-like cells can be isolated from multiple peripheral organs and maintained in neurosphere culture. Combining in vitro culture and transplantation, we show that expanded embryonic NCSC-like cells lose PNS traits and are reprogrammed to generate CNS cell types. When transplanted into the embryonic or adult mouse CNS, they differentiate predominantly into cells of the oligodendrocyte lineage without any signs of tumor formation. NCSC-derived oligodendrocytes generate CNS myelin and contribute to the repair of the myelin deficiency in shiverer mice. These results demonstrate a reprogramming of PNS progenitors to CNS fates without genetic modification and imply that PNS cells could be a potential source for cell-based CNS therapy.

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Sprache(n): eng - English
 Datum: 2011
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: eDoc: 579068
ISI: 000289934600014
 Art des Abschluß: -

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Titel: The Journal of Neuroscience
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 31 (17) Artikelnummer: - Start- / Endseite: 6379 - 6391 Identifikator: ISSN: 0270-6474