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Identification and characterization of a new source of adult human neural progenitors.
Behnan, Jinan; Stangeland, Biljana; Langella, Tiziana; Finocchiaro, Gaetano; Tringali, Giovanni; Meling, Torstein R; Murrell, Wayne.
Afiliación
  • Behnan J; Department of Immunology, Norwegian Center for Stem Cell Research, Institute of Clinical Medicine, Oslo University Hospital, Oslo, Norway.
  • Stangeland B; Department of Molecular Medicine, Institute of Basic Medical Sciences, The Medical Faculty, University of Oslo, Oslo, Norway.
  • Langella T; Department of Immunology, Norwegian Center for Stem Cell Research, Institute of Clinical Medicine, Oslo University Hospital, Oslo, Norway.
  • Finocchiaro G; Department of Insights and Data, Capgemini, Akershus, Norway.
  • Tringali G; Unit of Molecular Neuro-Oncology, Neurological Institute C, Besta, Milan, Italy.
  • Meling TR; Unit of Molecular Neuro-Oncology, Neurological Institute C, Besta, Milan, Italy.
  • Murrell W; Department of Neurosurgery, Neurological Institute C. Besta, Milan, Italy.
Cell Death Dis ; 8(8): e2991, 2017 08 10.
Article en En | MEDLINE | ID: mdl-28796246
Adult neural progenitor cells (aNPCs) are a potential source for cell based therapy for neurodegenerative diseases and traumatic brain injuries. These cells have been traditionally isolated from hippocampus, subventricular zone and white matter. However, there is still a need for an easily accessible source with better yield to counter the limitations of small surgical samples of previously characterized aNPCs. Here we show that ultrasonic aspirate (UA) samples currently considered as 'biological waste after surgery,' offer a good source for aNPCs. Furthermore, we show that culture conditions dictated the phenotype of cells across patients. The neurosphere-enriched cells were more similar to freshly isolated brain cells, while cells expanded adherently in serum conditions were similar to mesenchymal stem cells. However, cells expanded in these adherent conditions expressed some NPC and glial markers in addition to active canonical Wnt signaling. This suggests a mesenchymal-neuroectodermal hybrid nature of these cells. Finally, we show that UA-NPCs are comparable to those from neurogenic regions. Our findings suggest that UA samples can be used as a source for fresh and in vitro propagated aNPCs that could have various clinical applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Adultas / Células-Madre Neurales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cell Death Dis Año: 2017 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Adultas / Células-Madre Neurales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cell Death Dis Año: 2017 Tipo del documento: Article País de afiliación: Noruega