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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |