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dc.contributor.authorDrake, Adam
dc.contributor.authorChen, Qingfeng
dc.contributor.authorDong, Di
dc.contributor.authorLeskov, Ilya B.
dc.contributor.authorFragoso, Maria F.
dc.contributor.authorLi, Yan
dc.contributor.authorIliopoulou, Bettina P.
dc.contributor.authorHwang, William
dc.contributor.authorLodish, Harvey F.
dc.contributor.authorChen, Jianzhu
dc.date.accessioned2012-09-12T13:28:55Z
dc.date.available2012-09-12T13:28:55Z
dc.date.issued2010-12
dc.date.submitted2010-10
dc.identifier.issn1547-3287
dc.identifier.urihttp://hdl.handle.net/1721.1/72658
dc.description.abstractClinical and preclinical applications of human hematopoietic stem cells (HSCs) are often limited by scarcity of cells. Expanding human HSCs to increase their numbers while maintaining their stem cell properties has therefore become an important area of research. Here, we report a robust HSC coculture system wherein cord blood CD34+ CD133+ cells were cocultured with mesenchymal stem cells engineered to express angiopoietin-like-5 in a defined medium. After 11 days of culture, SCID repopulating cells were expanded 60-fold by limiting dilution assay in NOD-scid Il2rg−/− (NSG) mice. The cultured CD34+ CD133+ cells had similar engraftment potential to uncultured CD34+ CD133+ cells in competitive repopulation assays and were capable of efficient secondary reconstitution. Further, the expanded cells supported a robust multilineage reconstitution of human blood cells in NSG recipient mice, including a more efficient T-cell reconstitution. These results demonstrate that the expanded CD34+ CD133+ cells maintain both short-term and long-term HSC activities. To our knowledge, this 60-fold expansion of SCID repopulating cells is the best expansion of human HSCs reported to date. Further development of this coculture method for expanding human HSCs for clinical and preclinical applications is therefore warranted.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant number DK067356)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant number AI69208)en_US
dc.description.sponsorshipSingapore-MIT Alliance for Research and Technology Centeren_US
dc.description.sponsorshipAnna Fuller Postdoctoral Fellowshipen_US
dc.language.isoen_US
dc.publisherMary Ann Lieberten_US
dc.relation.isversionofhttp://dx.doi.org/10.1089/scd.2010.0456en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleMesenchymal stem cells secreting angiopoietin-like-5 support efficient expansion of human hematopoietic stem cells without compromising their repopulating potentialen_US
dc.typeArticleen_US
dc.identifier.citationKhoury, Maroun et al. “Mesenchymal Stem Cells Secreting Angiopoietin-Like-5 Support Efficient Expansion of Human Hematopoietic Stem Cells Without Compromising Their Repopulating Potential.” Stem Cells and Development 20.8 (2011): 1371–1381. Copyright © 2011 Mary Ann Liebert, Inc. publishers.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverChen, Jianzhu
dc.contributor.mitauthorDrake, Adam
dc.contributor.mitauthorChen, Qingfeng
dc.contributor.mitauthorDong, Di
dc.contributor.mitauthorLeskov, Ilya B.
dc.contributor.mitauthorFragoso, Maria F.
dc.contributor.mitauthorLi, Yan
dc.contributor.mitauthorIliopoulou, Bettina P.
dc.contributor.mitauthorLodish, Harvey F.
dc.contributor.mitauthorChen, Jianzhu
dc.relation.journalStem Cells and Developmenten_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKhoury, Maroun; Drake, Adam; Chen, Qingfeng; Dong, Di; Leskov, Ilya; Fragoso, Maria F.; Li, Yan; Iliopoulou, Bettina P.; Hwang, William; Lodish, Harvey F.; Chen, Jianzhuen
dc.identifier.orcidhttps://orcid.org/0000-0002-7029-7415
dc.identifier.orcidhttps://orcid.org/0000-0002-5687-6154
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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