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dc.contributor.authorCentanin, Lázaroen
dc.contributor.authorAnder, Janina -Jen
dc.contributor.authorHoeckendorf, Burkharden
dc.contributor.authorLust, Katharinaen
dc.contributor.authorKellner, Tanjaen
dc.contributor.authorKraemer, Isabelen
dc.contributor.authorUrbany, Cedricen
dc.contributor.authorHasel, Evaen
dc.contributor.authorHarris, Williamen
dc.contributor.authorSimons, Benjaminen
dc.contributor.authorWittbrodt, Joachimen
dc.date.accessioned2014-09-30T13:38:03Z
dc.date.available2014-09-30T13:38:03Z
dc.date.issued2014-08-19en
dc.identifier.citation(2014) Development 141: 1-11 doi:10.1242/dev.109892en
dc.identifier.issn0950-1991
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/246081
dc.description.abstractThe potency of post-embryonic stem cells can only be addressed in the living organism, by labeling single cells after embryonic development and following their descendants. Recently, transplantation experiments involving permanently labeled cells revealed multipotent neural stem cells (NSCs) of embryonic origin in the medaka retina. To analyse whether NSC potency is affected by developmental progression, as reported for the mammalian brain, we developed an inducible toolkit for clonal labeling and non-invasive fate tracking. We used this toolkit to address post-embryonic stem cells in different tissues and to functionally differentiate transient progenitor cells from permanent, bona fide stem cells in the retina. Using temporally controlled clonal induction, we showed that post-embryonic retinal NSCs are exclusively multipotent and give rise to the complete spectrum of cell types in the neural retina. Intriguingly, and in contrast to any other vertebrate stem cell system described so far, long-term analysis of clones indicates a preferential mode of asymmetric cell division. Moreover, following the behavior of clones before and after external stimuli, such as injuries, shows that NSCs in the retina maintained the preference for asymmetric cell division during regenerative responses. We present a comprehensive analysis of individual post-embryonic NSCs in their physiological environment and establish the teleost retina as an ideal model for studying adult stem cell biology at single cell resolution.
dc.languageen_USen
dc.language.isoen_USen
dc.publisherThe Company of Biologists Ltd.
dc.rightsAttribution 2.0 UK: England & Wales*
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/uk/*
dc.titleExclusive Multipotency and Preferential Asymmetric Divisions in Post-Embryonic Neural Stem Cells of the Fish Retinaen
dc.typeArticle
dc.description.versionThis is the final version of the article. It has been published by The Company of Biologists Ltd in Development here: http://dev.biologists.org/content/early/2014/08/19/dev.109892.long.en
prism.endingPage11
prism.publicationDate2014en
prism.publicationNameDevelopmenten
prism.startingPage1
prism.volume141en
dc.rioxxterms.funderWellcome Trust German Science Funding Agency European Research Council
dc.rioxxterms.projectidWT: 098357/Z/12/Z German Science Funding Agency: SFB 873
rioxxterms.versionofrecord10.1242/dev.109892en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2014-08-19en
dc.contributor.orcidHarris, William [0000-0002-9995-8096]
dc.contributor.orcidSimons, Benjamin [0000-0002-3875-7071]
dc.identifier.eissn1477-9129
rioxxterms.typeJournal Article/Reviewen
pubs.funder-project-idWELLCOME TRUST (098357/Z/12/Z)
pubs.funder-project-idWellcome Trust (100329/Z/12/Z)
pubs.funder-project-idWellcome Trust (092096/Z/10/Z)


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Attribution 2.0 UK: England & Wales
Except where otherwise noted, this item's licence is described as Attribution 2.0 UK: England & Wales