Cargando…

Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres

Neural Stem and Progenitor Cells (NSC/NPC) are gathering tangible recognition for their uses in cell therapy and cell replacement therapies for human disease, as well as a model system to continue research on overall neural developmental processes in vitro. The Subventricular Zone is one of the larg...

Descripción completa

Detalles Bibliográficos
Autores principales: Franco, Paula G., Pasquini, Juana M., Silvestroff, Lucas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383518/
https://www.ncbi.nlm.nih.gov/pubmed/25837625
http://dx.doi.org/10.1371/journal.pone.0121774
_version_ 1782364751953657856
author Franco, Paula G.
Pasquini, Juana M.
Silvestroff, Lucas
author_facet Franco, Paula G.
Pasquini, Juana M.
Silvestroff, Lucas
author_sort Franco, Paula G.
collection PubMed
description Neural Stem and Progenitor Cells (NSC/NPC) are gathering tangible recognition for their uses in cell therapy and cell replacement therapies for human disease, as well as a model system to continue research on overall neural developmental processes in vitro. The Subventricular Zone is one of the largest NSC/NPC niches in the developing mammalian Central Nervous System, and persists through to adulthood. Oligodendrocyte progenitor cell (OPC) enriched cultures are usefull tools for in vitro studies as well as for cell replacement therapies for treating demyelination diseases. We used Subventricular Zone-derived NSC/NPC primary cultures from newborn mice and compared the effects of different growth factor combinations on cell proliferation and OPC yield. The Platelet Derived Growth Factor-AA and BB homodimers had a positive and significant impact on OPC generation. Furthermore, heparin addition to the culture media contributed to further increase overall culture yields. The OPC generated by this protocol were able to mature into Myelin Basic Protein-expressing cells and to interact with neurons in an in vitro co-culture system. As a whole, we describe an optimized in vitro method for increasing OPC.
format Online
Article
Text
id pubmed-4383518
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43835182015-04-09 Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres Franco, Paula G. Pasquini, Juana M. Silvestroff, Lucas PLoS One Research Article Neural Stem and Progenitor Cells (NSC/NPC) are gathering tangible recognition for their uses in cell therapy and cell replacement therapies for human disease, as well as a model system to continue research on overall neural developmental processes in vitro. The Subventricular Zone is one of the largest NSC/NPC niches in the developing mammalian Central Nervous System, and persists through to adulthood. Oligodendrocyte progenitor cell (OPC) enriched cultures are usefull tools for in vitro studies as well as for cell replacement therapies for treating demyelination diseases. We used Subventricular Zone-derived NSC/NPC primary cultures from newborn mice and compared the effects of different growth factor combinations on cell proliferation and OPC yield. The Platelet Derived Growth Factor-AA and BB homodimers had a positive and significant impact on OPC generation. Furthermore, heparin addition to the culture media contributed to further increase overall culture yields. The OPC generated by this protocol were able to mature into Myelin Basic Protein-expressing cells and to interact with neurons in an in vitro co-culture system. As a whole, we describe an optimized in vitro method for increasing OPC. Public Library of Science 2015-04-02 /pmc/articles/PMC4383518/ /pubmed/25837625 http://dx.doi.org/10.1371/journal.pone.0121774 Text en © 2015 Franco et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Franco, Paula G.
Pasquini, Juana M.
Silvestroff, Lucas
Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title_full Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title_fullStr Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title_full_unstemmed Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title_short Optimizing Culture Medium Composition to Improve Oligodendrocyte Progenitor Cell Yields In Vitro from Subventricular Zone-Derived Neural Progenitor Cell Neurospheres
title_sort optimizing culture medium composition to improve oligodendrocyte progenitor cell yields in vitro from subventricular zone-derived neural progenitor cell neurospheres
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383518/
https://www.ncbi.nlm.nih.gov/pubmed/25837625
http://dx.doi.org/10.1371/journal.pone.0121774
work_keys_str_mv AT francopaulag optimizingculturemediumcompositiontoimproveoligodendrocyteprogenitorcellyieldsinvitrofromsubventricularzonederivedneuralprogenitorcellneurospheres
AT pasquinijuanam optimizingculturemediumcompositiontoimproveoligodendrocyteprogenitorcellyieldsinvitrofromsubventricularzonederivedneuralprogenitorcellneurospheres
AT silvestrofflucas optimizingculturemediumcompositiontoimproveoligodendrocyteprogenitorcellyieldsinvitrofromsubventricularzonederivedneuralprogenitorcellneurospheres