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dc.contributor.authorMunoz, SS
dc.contributor.authorEngel, M
dc.contributor.authorBalez, R
dc.contributor.authorDo-Ha, D
dc.contributor.authorCabral-da-Silva, MC
dc.contributor.authorHernandez, D
dc.contributor.authorBerg, T
dc.contributor.authorFifita, JA
dc.contributor.authorGrima, N
dc.contributor.authorYang, S
dc.contributor.authorBlair, IP
dc.contributor.authorNicholson, G
dc.contributor.authorCook, AL
dc.contributor.authorHewitt, AW
dc.contributor.authorPebay, A
dc.contributor.authorOoi, L
dc.date.accessioned2020-11-17T03:44:20Z
dc.date.available2020-11-17T03:44:20Z
dc.date.issued2020-09-01
dc.identifierpii: cells9092018
dc.identifier.citationMunoz, S. S., Engel, M., Balez, R., Do-Ha, D., Cabral-da-Silva, M. C., Hernandez, D., Berg, T., Fifita, J. A., Grima, N., Yang, S., Blair, I. P., Nicholson, G., Cook, A. L., Hewitt, A. W., Pebay, A. & Ooi, L. (2020). A Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer's Disease and Frontotemporal Dementia Disease Modeling. CELLS, 9 (9), https://doi.org/10.3390/cells9092018.
dc.identifier.issn2073-4409
dc.identifier.urihttp://hdl.handle.net/11343/251588
dc.description.abstractThe study of neurodegenerative diseases using pluripotent stem cells requires new methods to assess neurodevelopment and neurodegeneration of specific neuronal subtypes. The cholinergic system, characterized by its use of the neurotransmitter acetylcholine, is one of the first to degenerate in Alzheimer's disease and is also affected in frontotemporal dementia. We developed a differentiation protocol to generate basal forebrain-like cholinergic neurons (BFCNs) from induced pluripotent stem cells (iPSCs) aided by the use of small molecule inhibitors and growth factors. Ten iPSC lines were successfully differentiated into BFCNs using this protocol. The neuronal cultures were characterised through RNA and protein expression, and functional analysis of neurons was confirmed by whole-cell patch clamp. We have developed a reliable protocol using only small molecule inhibitors and growth factors, while avoiding transfection or cell sorting methods, to achieve a BFCN culture that expresses the characteristic markers of cholinergic neurons.
dc.languageEnglish
dc.publisherMDPI
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleA Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer's Disease and Frontotemporal Dementia Disease Modeling
dc.typeJournal Article
dc.identifier.doi10.3390/cells9092018
melbourne.affiliation.departmentSurgery (RMH)
melbourne.affiliation.departmentCentre for Eye Research Australia (CERA)
melbourne.affiliation.departmentAnatomy and Neuroscience
melbourne.source.titleCells
melbourne.source.volume9
melbourne.source.issue9
dc.rights.licenseCC BY
melbourne.elementsid1465504
melbourne.contributor.authorPebay, Alice
melbourne.contributor.authorHernandez De Santiago, Hector
dc.identifier.eissn2073-4409
melbourne.accessrightsOpen Access


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