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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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