Cited 8 times in
Behavioral improvement after transplantation of neural precursors derived from embryonic stem cells into the globally ischemic brain of adolescent rats
DC Field | Value | Language |
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dc.contributor.author | 김흥동 | - |
dc.contributor.author | 이진성 | - |
dc.contributor.author | 강훈철 | - |
dc.contributor.author | 김대성 | - |
dc.contributor.author | 김동욱 | - |
dc.contributor.author | 김지영 | - |
dc.contributor.author | 김한수 | - |
dc.date.accessioned | 2015-04-23T16:58:26Z | - |
dc.date.available | 2015-04-23T16:58:26Z | - |
dc.date.issued | 2010 | - |
dc.identifier.issn | 0387-7604 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/101584 | - |
dc.description.abstract | We intended to determine whether transplanted neural precursors, derived from mouse embryonic stem (ES) cells, can migrate and differentiate into mature neurons and glial cells in damaged brains and improve functional deficits caused by global cerebral ischemic injury in adolescent rats. METHODS: Global ischemia was induced using the four-vessel occlusion method. ES cells that display enhanced expression of yellow fluorescent protein were co-cultured in N2 supplemented media with PA6 cells that had stromal derived inducing activity. Neural precursor cells were directly transplanted bilaterally into hippocampal C3 areas 2 weeks after induction of global ischemia. Assessments of the Morris water-maze test at eight weeks and, the Open field activity levels at two, four, six and eight weeks after transplantation were carried out according to standard methods. RESULTS: From neural precursors, we were able to generate neural lineages, including neurons and glial cells in vitro. Eight weeks following transplantation, cellular migration as well as generation of neural cells including neurons, astrocytes, and oligodendrocytes developed from the grafted ES cell-derived neural precursors were observed. Cell-transplanted animals exhibited enhanced functional recovery on sensorimotor and behavioral tests, compared to vehicle-treated control animals. CONCLUSION: Therefore, transplantation of mouse ES cell-derived neural precursor cells shows promise for improving recovery after global ischemia in adolescent rats. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 658~668 | - |
dc.relation.isPartOf | BRAIN & DEVELOPMENT | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Behavior, Animal/physiology* | - |
dc.subject.MESH | Biomarkers/metabolism | - |
dc.subject.MESH | Brain Ischemia/pathology | - |
dc.subject.MESH | Brain Ischemia/physiopathology | - |
dc.subject.MESH | Brain Ischemia/rehabilitation* | - |
dc.subject.MESH | Brain Ischemia/surgery* | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Coculture Techniques | - |
dc.subject.MESH | Embryonic Stem Cells/cytology | - |
dc.subject.MESH | Embryonic Stem Cells/physiology* | - |
dc.subject.MESH | Fluorescent Dyes/metabolism | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Neuropsychological Tests | - |
dc.subject.MESH | Rats | - |
dc.subject.MESH | Rats, Sprague-Dawley | - |
dc.subject.MESH | Stem Cell Transplantation* | - |
dc.subject.MESH | Stem Cells/cytology | - |
dc.subject.MESH | Stem Cells/physiology* | - |
dc.title | Behavioral improvement after transplantation of neural precursors derived from embryonic stem cells into the globally ischemic brain of adolescent rats | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Anesthesiology (마취통증의학) | - |
dc.contributor.googleauthor | Hoon-Chul Kanga | - |
dc.contributor.googleauthor | Dae-Sung Kimb | - |
dc.contributor.googleauthor | Ji Young Kimb | - |
dc.contributor.googleauthor | Han-Soo Kimc | - |
dc.contributor.googleauthor | Bo Young Limb | - |
dc.contributor.googleauthor | Heung Dong Kima | - |
dc.contributor.googleauthor | Jin-Sung Leed | - |
dc.contributor.googleauthor | Baik-Lin Eun | - |
dc.contributor.googleauthor | Dong-Wook Kim | - |
dc.identifier.doi | 10.1016/j.braindev.2009.09.010 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00367 | - |
dc.contributor.localId | A01208 | - |
dc.contributor.localId | A00102 | - |
dc.contributor.localId | A01100 | - |
dc.contributor.localId | A03227 | - |
dc.contributor.localId | A00406 | - |
dc.contributor.localId | A00981 | - |
dc.relation.journalcode | J00386 | - |
dc.identifier.eissn | 1872-7131 | - |
dc.identifier.pmid | 19854013 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0387760409002538 | - |
dc.subject.keyword | Embryonic stem cells | - |
dc.subject.keyword | Neural precursors | - |
dc.subject.keyword | Globally ischemic brain | - |
dc.subject.keyword | Cell transplantation | - |
dc.contributor.alternativeName | Kim, Heung Dong | - |
dc.contributor.alternativeName | Lee, Jin Sung | - |
dc.contributor.alternativeName | Kang, Hoon Chul | - |
dc.contributor.alternativeName | Kim, Dae Sung | - |
dc.contributor.alternativeName | Kim, Dong Wook | - |
dc.contributor.alternativeName | Kim, Ji Young | - |
dc.contributor.alternativeName | Kim, Han Soo | - |
dc.contributor.affiliatedAuthor | Kim, Dae Sung | - |
dc.contributor.affiliatedAuthor | Kim, Heung Dong | - |
dc.contributor.affiliatedAuthor | Kang, Hoon Chul | - |
dc.contributor.affiliatedAuthor | Kim, Han Soo | - |
dc.contributor.affiliatedAuthor | Lee, Jin Sung | - |
dc.contributor.affiliatedAuthor | Kim, Dong Wook | - |
dc.contributor.affiliatedAuthor | Kim, Ji Young | - |
dc.citation.volume | 32 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 658 | - |
dc.citation.endPage | 668 | - |
dc.identifier.bibliographicCitation | BRAIN & DEVELOPMENT, Vol.32(8) : 658-668, 2010 | - |
dc.identifier.rimsid | 40104 | - |
dc.type.rims | ART | - |
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