Please use this identifier to cite or link to this item: https://doi.org/10.1186/2051-5960-2-4
Title: Generation of iPSC lines from archived non-cryoprotected biobanked dura mater
Authors: Sproul, A.A
Vensand, L.B
Dusenberry, C.R
Jacob, S
Vonsattel, J.P.G
Paull, D.J
Shelanski, M.L 
Crary, J.F
Noggle, S.A
Keywords: homeodomain protein
membrane antigen
NANOG protein, human
octamer transcription factor 4
proteoglycan
stage specific embryo antigen
stage-specific embryonic antigen-4
TRA-1-60 antigen, human
Alzheimer disease
animal
cell differentiation
cell proliferation
cytology
data base
degenerative disease
dura mater
fibroblast
human
metabolism
mouse
pathology
physiology
pluripotent stem cell
postmortem change
skin
transformed cell line
virology
Alzheimer Disease
Animals
Antigens, Surface
Cell Differentiation
Cell Line, Transformed
Cell Proliferation
Databases as Topic
Dura Mater
Fibroblasts
Homeodomain Proteins
Humans
Induced Pluripotent Stem Cells
Mice
Neurodegenerative Diseases
Octamer Transcription Factor-3
Postmortem Changes
Proteoglycans
Skin
Stage-Specific Embryonic Antigens
Issue Date: 2014
Citation: Sproul, A.A, Vensand, L.B, Dusenberry, C.R, Jacob, S, Vonsattel, J.P.G, Paull, D.J, Shelanski, M.L, Crary, J.F, Noggle, S.A (2014). Generation of iPSC lines from archived non-cryoprotected biobanked dura mater. Acta Neuropathologica Communications 2 (1) : 4. ScholarBank@NUS Repository. https://doi.org/10.1186/2051-5960-2-4
Rights: Attribution 4.0 International
Abstract: 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. © 2014 Sproul et al.; licensee BioMed Central Ltd.
Source Title: Acta Neuropathologica Communications
URI: https://scholarbank.nus.edu.sg/handle/10635/182029
ISSN: 20515960
DOI: 10.1186/2051-5960-2-4
Rights: Attribution 4.0 International
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