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Generation of iPSC lines from archived non-cryoprotected biobanked dura mater
BACKGROUND: Induced pluripotent stem cells (iPSCs) derived from patients with neurodegenerative disease generally lack neuropathological confirmation, the gold standard for disease classification and grading of severity. The use of tissue with a definitive neuropathological diagnosis would be an ide...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895779/ https://www.ncbi.nlm.nih.gov/pubmed/24398250 http://dx.doi.org/10.1186/2051-5960-2-4 |
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author | Sproul, Andrew A Vensand, Lauren B Dusenberry, Carmen R Jacob, Samson Vonsattel, Jean Paul G Paull, Daniel J Shelanski, Michael L Crary, John F Noggle, Scott A |
author_facet | Sproul, Andrew A Vensand, Lauren B Dusenberry, Carmen R Jacob, Samson Vonsattel, Jean Paul G Paull, Daniel J Shelanski, Michael L Crary, John F Noggle, Scott A |
author_sort | Sproul, Andrew A |
collection | PubMed |
description | BACKGROUND: Induced pluripotent stem cells (iPSCs) derived from patients with neurodegenerative disease generally lack neuropathological confirmation, the gold standard for disease classification and grading of severity. The use of tissue with a definitive neuropathological diagnosis would be an ideal source for iPSCs. The challenge to this approach is that the majority of biobanked brain tissue was not meant for growing live cells, and thus was not frozen in the presence of cryoprotectants such as DMSO. RESULTS: We report the generation of iPSCs from frozen non-cryoprotected dural tissue stored at −80°C for up to 11 years. This autopsy cohort included subjects with Alzheimer’s disease and four other neurodegenerative diseases. CONCLUSIONS: Disease-specific iPSCs can be generated from readily available, archival biobanked tissue. This allows for rapid expansion of generating iPSCs with confirmed pathology as well as allowing access to rare patient variants that have been banked. |
format | Online Article Text |
id | pubmed-3895779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38957792014-01-21 Generation of iPSC lines from archived non-cryoprotected biobanked dura mater Sproul, Andrew A Vensand, Lauren B Dusenberry, Carmen R Jacob, Samson Vonsattel, Jean Paul G Paull, Daniel J Shelanski, Michael L Crary, John F Noggle, Scott A Acta Neuropathol Commun Methodology Article BACKGROUND: Induced pluripotent stem cells (iPSCs) derived from patients with neurodegenerative disease generally lack neuropathological confirmation, the gold standard for disease classification and grading of severity. The use of tissue with a definitive neuropathological diagnosis would be an ideal source for iPSCs. The challenge to this approach is that the majority of biobanked brain tissue was not meant for growing live cells, and thus was not frozen in the presence of cryoprotectants such as DMSO. RESULTS: We report the generation of iPSCs from frozen non-cryoprotected dural tissue stored at −80°C for up to 11 years. This autopsy cohort included subjects with Alzheimer’s disease and four other neurodegenerative diseases. CONCLUSIONS: Disease-specific iPSCs can be generated from readily available, archival biobanked tissue. This allows for rapid expansion of generating iPSCs with confirmed pathology as well as allowing access to rare patient variants that have been banked. BioMed Central 2014-01-07 /pmc/articles/PMC3895779/ /pubmed/24398250 http://dx.doi.org/10.1186/2051-5960-2-4 Text en Copyright © 2014 Sproul 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Sproul, Andrew A Vensand, Lauren B Dusenberry, Carmen R Jacob, Samson Vonsattel, Jean Paul G Paull, Daniel J Shelanski, Michael L Crary, John F Noggle, Scott A Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title | Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title_full | Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title_fullStr | Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title_full_unstemmed | Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title_short | Generation of iPSC lines from archived non-cryoprotected biobanked dura mater |
title_sort | generation of ipsc lines from archived non-cryoprotected biobanked dura mater |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895779/ https://www.ncbi.nlm.nih.gov/pubmed/24398250 http://dx.doi.org/10.1186/2051-5960-2-4 |
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