Show simple item record

dc.contributor.authorWagner, D. E.
dc.contributor.authorWang, Irving E.
dc.contributor.authorReddien, Peter
dc.date.accessioned2017-07-07T18:52:14Z
dc.date.available2017-07-07T18:52:14Z
dc.date.issued2011-05
dc.date.submitted2011-02
dc.identifier.issn0036-8075
dc.identifier.issn1095-9203
dc.identifier.urihttp://hdl.handle.net/1721.1/110557
dc.description.abstractPluripotent cells in the embryo can generate all cell types, but lineage-restricted cells are generally thought to replenish adult tissues. Planarians are flatworms and regenerate from tiny body fragments, a process requiring a population of proliferating cells (neoblasts). Whether regeneration is accomplished by pluripotent cells or by the collective activity of multiple lineage-restricted cell types is unknown. We used ionizing radiation and single-cell transplantation to identify neoblasts that can form large descendant-cell colonies in vivo. These clonogenic neoblasts (cNeoblasts) produce cells that differentiate into neuronal, intestinal, and other known postmitotic cell types and are distributed throughout the body. Single transplanted cNeoblasts restored regeneration in lethally irradiated hosts. We conclude that broadly distributed, adult pluripotent stem cells underlie the remarkable regenerative abilities of planarians.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01GM080639)en_US
dc.language.isoen_US
dc.publisherAmerican Association for the Advancement of Science (AAAS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1126/science.1203983en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleClonogenic Neoblasts Are Pluripotent Adult Stem Cells That Underlie Planarian Regenerationen_US
dc.typeArticleen_US
dc.identifier.citationWagner, D. E.; Wang, I. E. and Reddien, P. W. “Clonogenic Neoblasts Are Pluripotent Adult Stem Cells That Underlie Planarian Regeneration.” Science 332, 6031 (May 2011): 811–816 © 2011 American Association for the Advancement of Science (AAAS)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorWang, Irving E.
dc.contributor.mitauthorReddien, Peter
dc.relation.journalScienceen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWagner, D. E.; Wang, I. E.; Reddien, P. W.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5569-333X
mit.licenseOPEN_ACCESS_POLICYen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record