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dc.contributor.authorCarlone, Diana L
dc.contributor.authorRiba-Wolman, Rebecca D
dc.contributor.authorDeary, Luke T
dc.contributor.authorTovaglieri, Alessio
dc.contributor.authorJiang, Lijie
dc.contributor.authorAmbruzs, Dana M
dc.contributor.authorMead, Benjamin E
dc.contributor.authorShah, Manasvi S
dc.contributor.authorLengner, Christopher J
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorBreault, David T
dc.date.accessioned2021-10-27T19:57:29Z
dc.date.available2021-10-27T19:57:29Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/133982
dc.description.abstract©2021 The Authors. Stem Cells published by Wiley Periodicals LLC on behalf of AlphaMed Press. Skeletal progenitor/stem cells (SSCs) play a critical role in postnatal bone growth and maintenance. Telomerase (Tert) activity prevents cellular senescence and is required for maintenance of stem cells in self-renewing tissues. Here we investigated the role of mTert-expressing cells in postnatal mouse long bone and found that mTert expression is enriched at the time of adolescent bone growth. mTert-GFP+ cells were identified in regions known to house SSCs, including the metaphyseal stroma, growth plate, and the bone marrow. We also show that mTert-expressing cells are a distinct SSC population with enriched colony-forming capacity and contribute to multiple mesenchymal lineages, in vitro. In contrast, in vivo lineage-tracing studies identified mTert+ cells as osteochondral progenitors and contribute to the bone-forming cell pool during endochondral bone growth with a subset persisting into adulthood. Taken together, our results show that mTert expression is temporally regulated and marks SSCs during a discrete phase of transitional growth between rapid bone growth and maintenance.
dc.language.isoen
dc.publisherWiley
dc.relation.isversionof10.1002/stem.3318
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceWiley
dc.titleTelomerase expression marks transitional growth-associated skeletal progenitor/stem cells: mTert marks skeletal progenitor/stem cells
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentWhitehead Institute for Biomedical Research
dc.relation.journalStem Cells
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-19T17:45:05Z
dspace.orderedauthorsCarlone, DL; Riba-Wolman, RD; Deary, LT; Tovaglieri, A; Jiang, L; Ambruzs, DM; Mead, BE; Shah, MS; Lengner, CJ; Jaenisch, R; Breault, DT
dspace.date.submission2021-07-19T17:45:09Z
mit.journal.volume39
mit.journal.issue3
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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