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Article: Striatal extracts promote the dopaminergic differentiation of GFP-bone mesenchymal stem cells

TitleStriatal extracts promote the dopaminergic differentiation of GFP-bone mesenchymal stem cells
Authors
KeywordsDopaminergic differentiation
GFP transgenic mice
Striatal extracts
Issue Date2012
Citation
Neuroscience Letters, 2012, v. 530, n. 2, p. 115-120 How to Cite?
AbstractBone mesenchymal stem cells (BMSCs) are an attractive donor graft source because of the potential of self-renewal and multi-direction differentiation. However, it is a great challenge to induce BMSCs to specifically differentiate to dopamine (DA) neurons for the treatment of Parkinson's disease. Because the striatum is the target tissue for the projection of DA neurons in the midbrain, we investigated whether its extracts could promote the dopaminergic differentiation of BMSCs. BMSCs were isolated from green fluorescent protein (GFP) transgenic mice. Flow cytometry was used to identify the expression of CD29 and CD11b in cultured BMSCs; and immunochemical staining was employed to determine the differentiation of BMSCs. Our results showed that striatal extracts could induce differentiation of BMSCs into both neurons and glia, especially the DA neurons. When transplanted to the rat striatum, GFP-BMSCs could differentiate into tyrosine hydroxylase positive neurons and demonstrate potential migration in the brain. Taking together, our results suggest that striatal extracts can specifically promote the dopaminergic differentiation of GFP-BMSCs, thereby providing a feasible strategy for the treatment of Parkinson's disease. © 2012 Published by Elsevier Ireland Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/325251
ISSN
2021 Impact Factor: 3.197
2020 SCImago Journal Rankings: 0.944

 

DC FieldValueLanguage
dc.contributor.authorYang, Shuhua-
dc.contributor.authorGao, Qing-
dc.contributor.authorBao, Lihua-
dc.contributor.authorZhang, Jing-
dc.contributor.authorHu, Yanlai-
dc.contributor.authorBing, Lujun-
dc.contributor.authorSun, Jinlong-
dc.contributor.authorHao, Jing-
dc.contributor.authorChen, Chao-
dc.contributor.authorLi, Shangzhi-
dc.contributor.authorPoon, W. S.-
dc.contributor.authorSun, Jinhao-
dc.contributor.authorGao, Yingmao-
dc.date.accessioned2023-02-27T07:30:58Z-
dc.date.available2023-02-27T07:30:58Z-
dc.date.issued2012-
dc.identifier.citationNeuroscience Letters, 2012, v. 530, n. 2, p. 115-120-
dc.identifier.issn0304-3940-
dc.identifier.urihttp://hdl.handle.net/10722/325251-
dc.description.abstractBone mesenchymal stem cells (BMSCs) are an attractive donor graft source because of the potential of self-renewal and multi-direction differentiation. However, it is a great challenge to induce BMSCs to specifically differentiate to dopamine (DA) neurons for the treatment of Parkinson's disease. Because the striatum is the target tissue for the projection of DA neurons in the midbrain, we investigated whether its extracts could promote the dopaminergic differentiation of BMSCs. BMSCs were isolated from green fluorescent protein (GFP) transgenic mice. Flow cytometry was used to identify the expression of CD29 and CD11b in cultured BMSCs; and immunochemical staining was employed to determine the differentiation of BMSCs. Our results showed that striatal extracts could induce differentiation of BMSCs into both neurons and glia, especially the DA neurons. When transplanted to the rat striatum, GFP-BMSCs could differentiate into tyrosine hydroxylase positive neurons and demonstrate potential migration in the brain. Taking together, our results suggest that striatal extracts can specifically promote the dopaminergic differentiation of GFP-BMSCs, thereby providing a feasible strategy for the treatment of Parkinson's disease. © 2012 Published by Elsevier Ireland Ltd.-
dc.languageeng-
dc.relation.ispartofNeuroscience Letters-
dc.subjectDopaminergic differentiation-
dc.subjectGFP transgenic mice-
dc.subjectStriatal extracts-
dc.titleStriatal extracts promote the dopaminergic differentiation of GFP-bone mesenchymal stem cells-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.neulet.2012.09.063-
dc.identifier.pmid23069670-
dc.identifier.scopuseid_2-s2.0-84868446938-
dc.identifier.volume530-
dc.identifier.issue2-
dc.identifier.spage115-
dc.identifier.epage120-
dc.identifier.eissn1872-7972-

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