Generation of disease-specific autopsy-confirmed iPSCs lines from postmortem isolated Peripheral Blood Mononuclear Cells
Autor: | Francelethia S. Shabazz, David A. Davis, Aleena Ali, Derek M. Dykxhoorn, Karen Nuytemans, William K. Scott, Deborah C. Mash, Jeffrey M. Vance, Juan L. Young, Kinsley C. Belle |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Pathology medicine.medical_specialty Cell type Cellular differentiation Induced Pluripotent Stem Cells Autopsy Cell Separation Disease Peripheral blood mononuclear cell Pathogenesis 03 medical and health sciences 0302 clinical medicine medicine Humans Induced pluripotent stem cell Neurons business.industry General Neuroscience Cell Differentiation Neurodegenerative Diseases Fibroblasts 030104 developmental biology Leukocytes Mononuclear Stem cell business 030217 neurology & neurosurgery |
Zdroj: | Neuroscience Letters. 637:201-206 |
ISSN: | 0304-3940 |
DOI: | 10.1016/j.neulet.2016.10.065 |
Popis: | Understanding the molecular mechanisms that underlie neurodegenerative disorders has been hampered by a lack of readily available model systems that replicate the complexity of the human disease. Recent advances in stem cell technology have facilitated the derivation of patient-specific stem cells from a variety of differentiated cell types. These induced pluripotent stem cells (iPSCs) are attractive disease models since they can be grown and differentiated to produce large numbers of disease-relevant cell types. However, most iPSC lines are derived in advance of, and without the benefit of, neuropathological confirmation of the donor - the gold standard for many disease classifications and measurement of disease severity. While others have reported the generation of autopsy-confirmed iPSC lines from patient explants, these methods require outgrowth of cadaver tissue, which require additional time and is often only successful ∼50% of the time. Here we report the rapid generation of autopsy-confirmed iPSC lines from peripheral blood mononuclear cells (PBMCs) drawn postmortem. Since this approach doesn't require the propagation of previously frozen cadaver tissue, iPSC can be rapidly and efficiently produced from patients with autopsy-confirmed pathology. These matched iPSC-derived patient-specific neurons and postmortem brain tissue will support studies of specific mechanisms that drive the pathogenesis of neurodegenerative diseases. |
Databáze: | OpenAIRE |
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