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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 |
Appears in Collections: | Elements Staff Publications |
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