The Preventive and Therapeutic Effects of Intravenous Human Adipose-Derived Stem Cells in Alzheimer's Disease Mice
DC Field | Value | Language |
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dc.contributor.author | Kim, Saeromi | - |
dc.contributor.author | Chang, Keun-A | - |
dc.contributor.author | Kim, Jeong A. | - |
dc.contributor.author | Park, Hyeong-Geun | - |
dc.contributor.author | Ra, Jeong Chan | - |
dc.contributor.author | Kim, Hye-Sun | - |
dc.contributor.author | Suh, Yoo-Hun | - |
dc.date.available | 2020-02-29T05:43:11Z | - |
dc.date.created | 2020-02-06 | - |
dc.date.issued | 2012-09-26 | - |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16162 | - |
dc.description.abstract | Alzheimer's disease (AD) is characterized by the accumulation of amyloid plaques and neurofibrillary tangles accompanied by cognitive dysfunction. The aim of the present study was to elucidate preventive and therapeutic potential of stem cells for AD. Among stem cells, autologous human adipose-derived stem cells (hASCs) elicit no immune rejection responses, tumorigenesis, or ethical problems. We found that intravenously transplanted hASCs passed through the BBB and migrated into the brain. The learning, memory and pathology in an AD mouse model (Tg2576) mice greatly improved for at least 4 months after intravenous injection of hASC. The number of amyloid plaques and A beta levels decreased significantly in the brains of hASC-injected Tg mice compared to those of Tg-sham mice. Here, we first report that intravenously or intracerebrally transplanted hASCs significantly rescues memory deficit and neuropathology, in the brains of Tg mice by upregulating IL-10 and VEGF and be a possible use for the prevention and treatment of AD. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | PUBLIC LIBRARY SCIENCE | - |
dc.relation.isPartOf | PLOS ONE | - |
dc.subject | STROMAL CELLS | - |
dc.subject | NEURONAL DIFFERENTIATION | - |
dc.subject | NEUROTROPHIC FACTORS | - |
dc.subject | TRANSGENIC MODEL | - |
dc.subject | AMYLOID-PROTEIN | - |
dc.subject | NERVOUS-SYSTEM | - |
dc.subject | GROWTH-FACTOR | - |
dc.subject | MOUSE MODEL | - |
dc.subject | IN-VITRO | - |
dc.subject | TRANSPLANTATION | - |
dc.title | The Preventive and Therapeutic Effects of Intravenous Human Adipose-Derived Stem Cells in Alzheimer's Disease Mice | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000309517300051 | - |
dc.identifier.doi | 10.1371/journal.pone.0045757 | - |
dc.identifier.bibliographicCitation | PLOS ONE, v.7, no.9 | - |
dc.identifier.scopusid | 2-s2.0-84866862490 | - |
dc.citation.title | PLOS ONE | - |
dc.citation.volume | 7 | - |
dc.citation.number | 9 | - |
dc.contributor.affiliatedAuthor | Chang, Keun-A | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | STROMAL CELLS | - |
dc.subject.keywordPlus | NEURONAL DIFFERENTIATION | - |
dc.subject.keywordPlus | NEUROTROPHIC FACTORS | - |
dc.subject.keywordPlus | TRANSGENIC MODEL | - |
dc.subject.keywordPlus | AMYLOID-PROTEIN | - |
dc.subject.keywordPlus | NERVOUS-SYSTEM | - |
dc.subject.keywordPlus | GROWTH-FACTOR | - |
dc.subject.keywordPlus | MOUSE MODEL | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | TRANSPLANTATION | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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