Cargando…

Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons

INTRODUCTION: The use of immortalized neural stem cells either as models of neural development in vitro or as cellular therapies in central nervous system (CNS) disorders has been controversial. This controversy has centered on the capacity of immortalized cells to retain characteristic features of...

Descripción completa

Detalles Bibliográficos
Autores principales: Cocks, Graham, Romanyuk, Nataliya, Amemori, Takashi, Jendelova, Pavla, Forostyak, Oksana, Jeffries, Aaron R, Perfect, Leo, Thuret, Sandrine, Dayanithi, Govindan, Sykova, Eva, Price, Jack
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706922/
https://www.ncbi.nlm.nih.gov/pubmed/23759128
http://dx.doi.org/10.1186/scrt220
_version_ 1782276435102138368
author Cocks, Graham
Romanyuk, Nataliya
Amemori, Takashi
Jendelova, Pavla
Forostyak, Oksana
Jeffries, Aaron R
Perfect, Leo
Thuret, Sandrine
Dayanithi, Govindan
Sykova, Eva
Price, Jack
author_facet Cocks, Graham
Romanyuk, Nataliya
Amemori, Takashi
Jendelova, Pavla
Forostyak, Oksana
Jeffries, Aaron R
Perfect, Leo
Thuret, Sandrine
Dayanithi, Govindan
Sykova, Eva
Price, Jack
author_sort Cocks, Graham
collection PubMed
description INTRODUCTION: The use of immortalized neural stem cells either as models of neural development in vitro or as cellular therapies in central nervous system (CNS) disorders has been controversial. This controversy has centered on the capacity of immortalized cells to retain characteristic features of the progenitor cells resident in the tissue of origin from which they were derived, and the potential for tumorogenicity as a result of immortalization. Here, we report the generation of conditionally immortalized neural stem cell lines from human fetal spinal cord tissue, which addresses these issues. METHODS: Clonal neural stem cell lines were derived from 10-week-old human fetal spinal cord and conditionally immortalized with an inducible form of cMyc. The derived lines were karyotyped, transcriptionally profiled by microarray, and assessed against a panel of spinal cord progenitor markers with immunocytochemistry. In addition, the lines were differentiated and assessed for the presence of neuronal fate markers and functional calcium channels. Finally, a clonal line expressing eGFP was grafted into lesioned rat spinal cord and assessed for survival, differentiation characteristics, and tumorogenicity. RESULTS: We demonstrate that these clonal lines (a) retain a clear transcriptional signature of ventral spinal cord progenitors and a normal karyotype after extensive propagation in vitro, (b) differentiate into relevant ventral neuronal subtypes with functional T-, L-, N-, and P/Q-type Ca(2+) channels and spontaneous calcium oscillations, and (c) stably engraft into lesioned rat spinal cord without tumorogenicity. CONCLUSIONS: We propose that these cells represent a useful tool both for the in vitro study of differentiation into ventral spinal cord neuronal subtypes, and for examining the potential of conditionally immortalized neural stem cells to facilitate functional recovery after spinal cord injury or disease.
format Online
Article
Text
id pubmed-3706922
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-37069222013-07-15 Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons Cocks, Graham Romanyuk, Nataliya Amemori, Takashi Jendelova, Pavla Forostyak, Oksana Jeffries, Aaron R Perfect, Leo Thuret, Sandrine Dayanithi, Govindan Sykova, Eva Price, Jack Stem Cell Res Ther Research INTRODUCTION: The use of immortalized neural stem cells either as models of neural development in vitro or as cellular therapies in central nervous system (CNS) disorders has been controversial. This controversy has centered on the capacity of immortalized cells to retain characteristic features of the progenitor cells resident in the tissue of origin from which they were derived, and the potential for tumorogenicity as a result of immortalization. Here, we report the generation of conditionally immortalized neural stem cell lines from human fetal spinal cord tissue, which addresses these issues. METHODS: Clonal neural stem cell lines were derived from 10-week-old human fetal spinal cord and conditionally immortalized with an inducible form of cMyc. The derived lines were karyotyped, transcriptionally profiled by microarray, and assessed against a panel of spinal cord progenitor markers with immunocytochemistry. In addition, the lines were differentiated and assessed for the presence of neuronal fate markers and functional calcium channels. Finally, a clonal line expressing eGFP was grafted into lesioned rat spinal cord and assessed for survival, differentiation characteristics, and tumorogenicity. RESULTS: We demonstrate that these clonal lines (a) retain a clear transcriptional signature of ventral spinal cord progenitors and a normal karyotype after extensive propagation in vitro, (b) differentiate into relevant ventral neuronal subtypes with functional T-, L-, N-, and P/Q-type Ca(2+) channels and spontaneous calcium oscillations, and (c) stably engraft into lesioned rat spinal cord without tumorogenicity. CONCLUSIONS: We propose that these cells represent a useful tool both for the in vitro study of differentiation into ventral spinal cord neuronal subtypes, and for examining the potential of conditionally immortalized neural stem cells to facilitate functional recovery after spinal cord injury or disease. BioMed Central 2013-06-07 /pmc/articles/PMC3706922/ /pubmed/23759128 http://dx.doi.org/10.1186/scrt220 Text en Copyright © 2013 Cocks et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cocks, Graham
Romanyuk, Nataliya
Amemori, Takashi
Jendelova, Pavla
Forostyak, Oksana
Jeffries, Aaron R
Perfect, Leo
Thuret, Sandrine
Dayanithi, Govindan
Sykova, Eva
Price, Jack
Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title_full Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title_fullStr Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title_full_unstemmed Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title_short Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons
title_sort conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional v2a interneurons and motorneurons
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706922/
https://www.ncbi.nlm.nih.gov/pubmed/23759128
http://dx.doi.org/10.1186/scrt220
work_keys_str_mv AT cocksgraham conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT romanyuknataliya conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT amemoritakashi conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT jendelovapavla conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT forostyakoksana conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT jeffriesaaronr conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT perfectleo conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT thuretsandrine conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT dayanithigovindan conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT sykovaeva conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons
AT pricejack conditionallyimmortalizedstemcelllinesfromhumanspinalcordretainregionalidentityandgeneratefunctionalv2ainterneuronsandmotorneurons