File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Umbilical cord-derived mesenchymal stem cells with forced expression of hepatocyte growth factor enhance remyelination and functional recovery in a rat intracerebral hemorrhage model

TitleUmbilical cord-derived mesenchymal stem cells with forced expression of hepatocyte growth factor enhance remyelination and functional recovery in a rat intracerebral hemorrhage model
Authors
KeywordsHepatocyte growth factor
Intracerebral hemorrhage
Mesenchymal stem cells
Regeneration
Remyelination
Transduction
Umbilical cord
Issue Date2010
Citation
Neurosurgery, 2010, v. 67, n. 2, p. 357-365 How to Cite?
AbstractBACKGROUND: Spontaneous intracerebral hemorrhage (ICH) carries a high mortality rate, with survivors commonly left with permanent neurological deficits. Mesenchymal stem cell (MSC) transplantation promotes functional recovery in experimental ICH, and treatment with hepatocyte growth factor (HGF) is beneficial in ischemic stroke. OBJECTIVE: We hypothesize that transplantation of MSCs with previous transduction of HGF has an additive effect in promoting neurological recovery through myelin and axonal regeneration. METHODS: HGF transduction to human umbilical cord-derived MSCs using lentiviral plasmid pWPI-HGF-GFP was prepared. One week after a collagenase-induced ICH, 80 male Sprague-Dawley rats were divided into 3 groups for stereotactic injection of phosphate-buffered saline (group I), MSC transplant (group II), and HGF-transduced MSC transplant (group III), respectively, into the left ventricle. The animals were assessed weekly for 5 weeks using the Rotarod motor function test, at which time they were killed for Luxol fast blue myelin staining and appropriate immunohistochemistry and Western blotting. RESULTS: Animals receiving transplanted HGF-transduced MSCs (group III) exhibited significantly better motor function recovery than animals treated with MSCs alone (group II), which in turn performed better than the phosphate-buffered saline controls at 2 weeks after transplantation. Luxol fast blue staining of myelin displayed significantly less demyelination and significantly higher reactivity in myelin basic protein and growth-associated protein-43 in immunohistochemistry and Western blotting and significantly reduced myelin-associated glycoprotein activity in group III animals. CONCLUSION: Animals transplanted with HGF-transduced MSCs 1 week after experimental ICH were shown to achieve a better neurological recovery. This improved neurological recovery from ICH is attributed to nerve fiber remyelination and axonal regeneration. Copyright © 2010 by the Congress of Neurological Surgeons.
Persistent Identifierhttp://hdl.handle.net/10722/325200
ISSN
2023 Impact Factor: 3.9
2023 SCImago Journal Rankings: 1.313
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, An Min-
dc.contributor.authorLu, Gang-
dc.contributor.authorTsang, Kam Sze-
dc.contributor.authorLi, Guo-
dc.contributor.authorWu, Yan-
dc.contributor.authorHuang, Zheng Song-
dc.contributor.authorNg, Ho Keung-
dc.contributor.authorKung, Hsiang Fu-
dc.contributor.authorPoon, Wai Sang-
dc.date.accessioned2023-02-27T07:30:32Z-
dc.date.available2023-02-27T07:30:32Z-
dc.date.issued2010-
dc.identifier.citationNeurosurgery, 2010, v. 67, n. 2, p. 357-365-
dc.identifier.issn0148-396X-
dc.identifier.urihttp://hdl.handle.net/10722/325200-
dc.description.abstractBACKGROUND: Spontaneous intracerebral hemorrhage (ICH) carries a high mortality rate, with survivors commonly left with permanent neurological deficits. Mesenchymal stem cell (MSC) transplantation promotes functional recovery in experimental ICH, and treatment with hepatocyte growth factor (HGF) is beneficial in ischemic stroke. OBJECTIVE: We hypothesize that transplantation of MSCs with previous transduction of HGF has an additive effect in promoting neurological recovery through myelin and axonal regeneration. METHODS: HGF transduction to human umbilical cord-derived MSCs using lentiviral plasmid pWPI-HGF-GFP was prepared. One week after a collagenase-induced ICH, 80 male Sprague-Dawley rats were divided into 3 groups for stereotactic injection of phosphate-buffered saline (group I), MSC transplant (group II), and HGF-transduced MSC transplant (group III), respectively, into the left ventricle. The animals were assessed weekly for 5 weeks using the Rotarod motor function test, at which time they were killed for Luxol fast blue myelin staining and appropriate immunohistochemistry and Western blotting. RESULTS: Animals receiving transplanted HGF-transduced MSCs (group III) exhibited significantly better motor function recovery than animals treated with MSCs alone (group II), which in turn performed better than the phosphate-buffered saline controls at 2 weeks after transplantation. Luxol fast blue staining of myelin displayed significantly less demyelination and significantly higher reactivity in myelin basic protein and growth-associated protein-43 in immunohistochemistry and Western blotting and significantly reduced myelin-associated glycoprotein activity in group III animals. CONCLUSION: Animals transplanted with HGF-transduced MSCs 1 week after experimental ICH were shown to achieve a better neurological recovery. This improved neurological recovery from ICH is attributed to nerve fiber remyelination and axonal regeneration. Copyright © 2010 by the Congress of Neurological Surgeons.-
dc.languageeng-
dc.relation.ispartofNeurosurgery-
dc.subjectHepatocyte growth factor-
dc.subjectIntracerebral hemorrhage-
dc.subjectMesenchymal stem cells-
dc.subjectRegeneration-
dc.subjectRemyelination-
dc.subjectTransduction-
dc.subjectUmbilical cord-
dc.titleUmbilical cord-derived mesenchymal stem cells with forced expression of hepatocyte growth factor enhance remyelination and functional recovery in a rat intracerebral hemorrhage model-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1227/01.NEU.0000371983.06278.B3-
dc.identifier.pmid20644422-
dc.identifier.scopuseid_2-s2.0-77954971944-
dc.identifier.volume67-
dc.identifier.issue2-
dc.identifier.spage357-
dc.identifier.epage365-
dc.identifier.isiWOS:000280105800030-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats