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Data defining markers of human neural stem cell lineage potential

Neural stem cells (NSCs) and neural progenitor cells (NPCs) are self-renewing and multipotent cells, however, NPCs are considered to be more lineage-restricted with a reduced self-renewing capacity. We present data comparing the expression of 21 markers encompassing pluripotency, self-renewal (NSC)...

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Autores principales: Oikari, Lotta E., Okolicsanyi, Rachel K., Griffiths, Lyn R., Haupt, Larisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773572/
https://www.ncbi.nlm.nih.gov/pubmed/26958640
http://dx.doi.org/10.1016/j.dib.2016.02.030
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author Oikari, Lotta E.
Okolicsanyi, Rachel K.
Griffiths, Lyn R.
Haupt, Larisa M.
author_facet Oikari, Lotta E.
Okolicsanyi, Rachel K.
Griffiths, Lyn R.
Haupt, Larisa M.
author_sort Oikari, Lotta E.
collection PubMed
description Neural stem cells (NSCs) and neural progenitor cells (NPCs) are self-renewing and multipotent cells, however, NPCs are considered to be more lineage-restricted with a reduced self-renewing capacity. We present data comparing the expression of 21 markers encompassing pluripotency, self-renewal (NSC) as well as neuronal and glial (astrocyte and oligodendrocyte) lineage specification and 28 extracellular proteoglycan (PG) genes and their regulatory enzymes between embryonic stem cell (ESC)-derived human NSCs (hNSC H9 cells, Thermo Fisher) and human cortex-derived normal human NPCs (nhNPCs, Lonza). The data demonstrates expression differences of multiple lineage and proteoglycan-associated genes between hNSC H9 cells and nhNPCs. Data interpretation of markers and proteoglycans defining NSC and neural cell lineage characterisation can be found in “Cell surface heparan sulfate proteoglycans as novel markers of human neural stem cell fate determination” (Oikari et al. 2015) [1].
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spelling pubmed-47735722016-03-08 Data defining markers of human neural stem cell lineage potential Oikari, Lotta E. Okolicsanyi, Rachel K. Griffiths, Lyn R. Haupt, Larisa M. Data Brief Data Article Neural stem cells (NSCs) and neural progenitor cells (NPCs) are self-renewing and multipotent cells, however, NPCs are considered to be more lineage-restricted with a reduced self-renewing capacity. We present data comparing the expression of 21 markers encompassing pluripotency, self-renewal (NSC) as well as neuronal and glial (astrocyte and oligodendrocyte) lineage specification and 28 extracellular proteoglycan (PG) genes and their regulatory enzymes between embryonic stem cell (ESC)-derived human NSCs (hNSC H9 cells, Thermo Fisher) and human cortex-derived normal human NPCs (nhNPCs, Lonza). The data demonstrates expression differences of multiple lineage and proteoglycan-associated genes between hNSC H9 cells and nhNPCs. Data interpretation of markers and proteoglycans defining NSC and neural cell lineage characterisation can be found in “Cell surface heparan sulfate proteoglycans as novel markers of human neural stem cell fate determination” (Oikari et al. 2015) [1]. Elsevier 2016-02-19 /pmc/articles/PMC4773572/ /pubmed/26958640 http://dx.doi.org/10.1016/j.dib.2016.02.030 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Oikari, Lotta E.
Okolicsanyi, Rachel K.
Griffiths, Lyn R.
Haupt, Larisa M.
Data defining markers of human neural stem cell lineage potential
title Data defining markers of human neural stem cell lineage potential
title_full Data defining markers of human neural stem cell lineage potential
title_fullStr Data defining markers of human neural stem cell lineage potential
title_full_unstemmed Data defining markers of human neural stem cell lineage potential
title_short Data defining markers of human neural stem cell lineage potential
title_sort data defining markers of human neural stem cell lineage potential
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773572/
https://www.ncbi.nlm.nih.gov/pubmed/26958640
http://dx.doi.org/10.1016/j.dib.2016.02.030
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