Conference Paper: Comparative proteomic analysis of mesenchymal stem cells derived from human bone marrow, umbilical cord and placenta: Implication in the migration

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TitleComparative proteomic analysis of mesenchymal stem cells derived from human bone marrow, umbilical cord and placenta: Implication in the migration
AuthorsLi, G4
Zhang, XA4
Wang, H4
Wang, X4
Meng, CL4
Chan, CY4
Yew, DTW4
Tsang, KS4
Li, K4
Tsai, SN4
Ngai, SM4
Han, ZC3
Lin, MCM2
He, ML4
Kung, HF1 4
Issue Date2011
CitationAdvances In Experimental Medicine And Biology, 2011, v. 720, p. 51-68 [How to Cite?]
DOI: http://dx.doi.org/10.1007/978-1-4614-0254-1_5
AbstractUmbilical cord (UC) and placenta (P) have been suggested as alternatives to bone marrow (BM) as sources of mesenchymal stem cells (MSC) for cell therapy, with both UC- and P-MSC possess immunophenotypic and functional characteristics similar to BM-MSC. However, under defined conditions, the migration capacity of BM- and P-MSC was found to be 5.9- and 3.2-folds higher than that of UC-MSC, respectively. By the use of 2-DE and combined MS and MS/MS analysis, six differentially expressed proteins were identified among these MSC samples, with five of them known to be involved in cell migration as migration enhancing or inhibiting proteins. Interestingly, the expression levels of those proteins reflect perfectly the migration capacity of corresponding MSC, which is also proved by in vitro overexpression and silencing techniques. Our study indicates that a bunch of migration-related proteins are pivotal in governing the migration capacity of MSC. © 2011 Springer Science+Business Media, LLC.
ISSN0065-2598
2011 Impact Factor: 1.093
2011 SCImago Journal Rankings: 0.177
DOIhttp://dx.doi.org/10.1007/978-1-4614-0254-1_5
ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorLi, G
dc.contributor.authorZhang, XA
dc.contributor.authorWang, H
dc.contributor.authorWang, X
dc.contributor.authorMeng, CL
dc.contributor.authorChan, CY
dc.contributor.authorYew, DTW
dc.contributor.authorTsang, KS
dc.contributor.authorLi, K
dc.contributor.authorTsai, SN
dc.contributor.authorNgai, SM
dc.contributor.authorHan, ZC
dc.contributor.authorLin, MCM
dc.contributor.authorHe, ML
dc.contributor.authorKung, HF
dc.date.accessioned2012-10-08T03:35:22Z
dc.date.available2012-10-08T03:35:22Z
dc.date.issued2011
dc.description.abstractUmbilical cord (UC) and placenta (P) have been suggested as alternatives to bone marrow (BM) as sources of mesenchymal stem cells (MSC) for cell therapy, with both UC- and P-MSC possess immunophenotypic and functional characteristics similar to BM-MSC. However, under defined conditions, the migration capacity of BM- and P-MSC was found to be 5.9- and 3.2-folds higher than that of UC-MSC, respectively. By the use of 2-DE and combined MS and MS/MS analysis, six differentially expressed proteins were identified among these MSC samples, with five of them known to be involved in cell migration as migration enhancing or inhibiting proteins. Interestingly, the expression levels of those proteins reflect perfectly the migration capacity of corresponding MSC, which is also proved by in vitro overexpression and silencing techniques. Our study indicates that a bunch of migration-related proteins are pivotal in governing the migration capacity of MSC. © 2011 Springer Science+Business Media, LLC.
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationAdvances In Experimental Medicine And Biology, 2011, v. 720, p. 51-68 [How to Cite?]
DOI: http://dx.doi.org/10.1007/978-1-4614-0254-1_5
dc.identifier.doihttp://dx.doi.org/10.1007/978-1-4614-0254-1_5
dc.identifier.epage68
dc.identifier.issn0065-2598
2011 Impact Factor: 1.093
2011 SCImago Journal Rankings: 0.177
dc.identifier.scopuseid_2-s2.0-80053910493
dc.identifier.spage51
dc.identifier.urihttp://hdl.handle.net/10722/168877
dc.identifier.volume720
dc.languageeng
dc.publisher.placeUnited States
dc.relation.ispartofAdvances in Experimental Medicine and Biology
dc.relation.referencesReferences in Scopus
dc.titleComparative proteomic analysis of mesenchymal stem cells derived from human bone marrow, umbilical cord and placenta: Implication in the migration
dc.typeConference_Paper
Author Affiliations
  1. Sun Yat-Sen University Cancer Center
  2. The University of Hong Kong
  3. Institute of Hematology and Blood Disease Hospital
  4. Chinese University of Hong Kong