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dc.contributor.authorHolland, Nicholas D.
dc.contributor.authorSomorjai, Ildiko M.L.
dc.date.accessioned2020-11-02T16:30:08Z
dc.date.available2020-11-02T16:30:08Z
dc.date.issued2020-10-17
dc.identifier271010680
dc.identifiere9ed16cc-6e5c-4224-a8f4-5271661b79f9
dc.identifier85092741801
dc.identifier000579268800001
dc.identifier.citationHolland , N D & Somorjai , I M L 2020 , ' Serial blockface SEM suggests that stem cells may participate in adult notochord growth in an invertebrate chordate, the Bahamas lancelet ' , EvoDevo , vol. 11 , 22 . https://doi.org/10.1186/s13227-020-00167-6en
dc.identifier.otherORCID: /0000-0001-5243-6664/work/83085995
dc.identifier.urihttps://hdl.handle.net/10023/20886
dc.descriptionFunding: Lancelet research at Scripps Institution of Oceanography is supported by NSF Grant IOS 1952567 to LZ Holland and ND Holland. Research in the Somorjai lab is funded by Wellcome Trust ISSF3 and EU Horizon 2020 grants INFRADEV4 [654248] and INFRA ASSEMBLE [930984].en
dc.description.abstractBackground : The cellular basis of adult growth in cephalochordates (lancelets or amphioxus) has received little attention. Lancelets and their constituent organs grow slowly but continuously during adult life. Here, we consider whether this slow organ growth involves tissue-specific stem cells. Specifically, we focus on the cell populations in the notochord of an adult lancelet and use serial blockface scanning electron microscopy (SBSEM) to reconstruct the three-dimensional fine structure of all the cells in a tissue volume considerably larger than normally imaged with this technique.  Results : In the notochordal region studied, we identified 10 cells with stem cell-like morphology at the posterior tip of the organ, 160 progenitor (Müller) cells arranged along its surface, and 385 highly differentiated lamellar cells constituting its core. Each cell type could clearly be distinguished on the basis of cytoplasmic density and overall cell shape. Moreover, because of the large sample size, transitions between cell types were obvious.  Conclusions : For the notochord of adult lancelets, a reasonable interpretation of our data indicates growth of the organ is based on stem cells that self-renew and also give rise to progenitor cells that, in turn, differentiate into lamellar cells. Our discussion compares the cellular basis of adult notochord growth among chordates in general. In the vertebrates, several studies implied that proliferating cells (chordoblasts) in the cortex of the organ might be stem cells. However, we think it is more likely that such cells actually constitute a progenitor population downstream from and maintained by inconspicuous stem cells. We venture to suggest that careful searches should find stem cells in the adult notochords of many vertebrates, although possibly not in the notochordal vestiges (nucleus pulposus regions) of mammals, where the presence of endogenous proliferating cells remains controversial.
dc.format.extent15
dc.format.extent3818051
dc.language.isoeng
dc.relation.ispartofEvoDevoen
dc.subjectAmphioxusen
dc.subjectCephalochordataen
dc.subjectIntervertebral discen
dc.subjectLanceleten
dc.subjectNotochorden
dc.subjectNucleus pulposusen
dc.subjectProgenitor cellen
dc.subjectSerial blockface scanning electron microscopy (SBSEM)en
dc.subjectStem cellen
dc.subjectQH301 Biologyen
dc.subjectEcology, Evolution, Behavior and Systematicsen
dc.subjectDevelopmental Biologyen
dc.subjectGeneticsen
dc.subjectNDASen
dc.subject.lccQH301en
dc.titleSerial blockface SEM suggests that stem cells may participate in adult notochord growth in an invertebrate chordate, the Bahamas lanceleten
dc.typeJournal articleen
dc.contributor.sponsorThe Wellcome Trusten
dc.contributor.sponsorEuropean Commissionen
dc.contributor.sponsorEuropean Commissionen
dc.contributor.institutionUniversity of St Andrews. Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. Marine Alliance for Science & Technology Scotlanden
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.identifier.doi10.1186/s13227-020-00167-6
dc.description.statusPeer revieweden
dc.identifier.grantnumberen
dc.identifier.grantnumber654248en
dc.identifier.grantnumber730984en


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