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Protein-Induced Pluripotent Stem Cells Ameliorate Cognitive Dysfunction and Reduce Aβ Deposition in a Mouse Model of Alzheimer's Disease
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dc.contributor.author Cha, Moon-Yong -
dc.contributor.author Kwon, Yoo-Wook -
dc.contributor.author Ahn, Hyo-Suk -
dc.contributor.author Jeong, Hyobin -
dc.contributor.author Lee, Yong Yook -
dc.contributor.author Moon, Minho -
dc.contributor.author Baik, Sung Hoon -
dc.contributor.author Kim, Dong Kyu -
dc.contributor.author Song, Hyundong -
dc.contributor.author Yi, Eugene C. -
dc.contributor.author Hwang, Dae Hee -
dc.contributor.author Kim, Hyo-Soo -
dc.contributor.author Mook-Jung, Inhee -
dc.date.available 2017-08-10T08:18:08Z -
dc.date.created 2017-08-09 -
dc.date.issued 2017-01 -
dc.identifier.issn 2157-6564 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/4249 -
dc.description.abstract Transplantation of stem cells into the brain attenuates functional deficits in the central nervous system via cell replacement, the release of specific neurotransmitters, and the production of neurotrophic factors. To identify patient-specific and safe stem cells for treating Alzheimer’s disease (AD), we generated induced pluripotent stem cells (iPSCs) derived from mouse skin fibroblasts by treating protein extracts of embryonic stem cells. These reprogrammed cells were pluripotent but nontumorigenic. Here, we report that protein-iPSCs differentiated into glial cells and decreased plaque depositions in the 5XFAD transgenic AD mouse model. We also found that transplanted protein-iPSCs mitigated the cognitive dysfunction observed in these mice. Proteomic analysis revealed that oligodendrocyte-related genes were upregulated in brains injected with protein-iPSCs, providing new insights into the potential function of protein-iPSCs. Taken together, our data indicate that protein-iPSCs might be a promising therapeutic approach for AD. © 2016 The Authors. -
dc.language English -
dc.publisher AlphaMed Press -
dc.title Protein-Induced Pluripotent Stem Cells Ameliorate Cognitive Dysfunction and Reduce Aβ Deposition in a Mouse Model of Alzheimer's Disease -
dc.type Article -
dc.identifier.doi 10.5966/sctm.2016-0081 -
dc.identifier.wosid 000398194800031 -
dc.identifier.scopusid 2-s2.0-85017371053 -
dc.identifier.bibliographicCitation Stem Cells Translational Medicine, v.6, no.1, pp.293 - 305 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor 5XFAD mice -
dc.subject.keywordAuthor Proteomic analysis -
dc.subject.keywordAuthor Oligodendrocyte -
dc.subject.keywordAuthor Alzheimer&apos -
dc.subject.keywordAuthor s disease -
dc.subject.keywordAuthor Protein-iPSC -
dc.subject.keywordPlus 5XFAD mice -
dc.subject.keywordPlus Activation -
dc.subject.keywordPlus Alzheimer&apos -
dc.subject.keywordPlus s Disease (AD) -
dc.subject.keywordPlus Amyloid Beta (A Beta) -
dc.subject.keywordPlus Central Nervous System -
dc.subject.keywordPlus Generation -
dc.subject.keywordPlus Identification -
dc.subject.keywordPlus Mechanisms -
dc.subject.keywordPlus Mice -
dc.subject.keywordPlus Mouse -
dc.subject.keywordPlus Oligodendrocyte -
dc.subject.keywordPlus Progenitor Cells -
dc.subject.keywordPlus Protein Ipsc -
dc.subject.keywordPlus Proteomic Analysis -
dc.citation.endPage 305 -
dc.citation.number 1 -
dc.citation.startPage 293 -
dc.citation.title Stem Cells Translational Medicine -
dc.citation.volume 6 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Cell Biology -
dc.relation.journalWebOfScienceCategory Cell & Tissue Engineering -
dc.type.docType Article -
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