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Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life
The dynamics of epithelial stem cells (SCs) that contribute to the formation and maintenance of the cornea are poorly understood. Here, we used K14CreER(T2)-Confetti (Confetti) mice, sophisticated imaging, and computational modeling to trace the origins and fate of these cells during embryogenesis a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639292/ https://www.ncbi.nlm.nih.gov/pubmed/28943255 http://dx.doi.org/10.1016/j.stemcr.2017.08.015 |
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author | Richardson, Alexander Lobo, Erwin P. Delic, Naomi C. Myerscough, Mary R. Lyons, J. Guy Wakefield, Denis Di Girolamo, Nick |
author_facet | Richardson, Alexander Lobo, Erwin P. Delic, Naomi C. Myerscough, Mary R. Lyons, J. Guy Wakefield, Denis Di Girolamo, Nick |
author_sort | Richardson, Alexander |
collection | PubMed |
description | The dynamics of epithelial stem cells (SCs) that contribute to the formation and maintenance of the cornea are poorly understood. Here, we used K14CreER(T2)-Confetti (Confetti) mice, sophisticated imaging, and computational modeling to trace the origins and fate of these cells during embryogenesis and adult life. We show that keratin-14 (K14(+))-expressing progenitors are defined and widely distributed across the E16.5 cornea, after which they undergo cycles of proliferation and dispersal prior to eyelid opening. K14(+) clonal patches disappear from the central cornea and are replaced by limbal-derived K14(+) streaks, a finding that aligned with bromodeoxyuridine label-retaining studies. We also elucidated the mechanism by which SC clones are lost during life and propose this is due to population asymmetry and neutral drift. Finally, we established that the occurrence of an equatorial migratory mid-line is a consequence of apoptosis in a narrow nasal-temporal region, the site where eyelids meet during blinking. |
format | Online Article Text |
id | pubmed-5639292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56392922017-10-20 Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life Richardson, Alexander Lobo, Erwin P. Delic, Naomi C. Myerscough, Mary R. Lyons, J. Guy Wakefield, Denis Di Girolamo, Nick Stem Cell Reports Article The dynamics of epithelial stem cells (SCs) that contribute to the formation and maintenance of the cornea are poorly understood. Here, we used K14CreER(T2)-Confetti (Confetti) mice, sophisticated imaging, and computational modeling to trace the origins and fate of these cells during embryogenesis and adult life. We show that keratin-14 (K14(+))-expressing progenitors are defined and widely distributed across the E16.5 cornea, after which they undergo cycles of proliferation and dispersal prior to eyelid opening. K14(+) clonal patches disappear from the central cornea and are replaced by limbal-derived K14(+) streaks, a finding that aligned with bromodeoxyuridine label-retaining studies. We also elucidated the mechanism by which SC clones are lost during life and propose this is due to population asymmetry and neutral drift. Finally, we established that the occurrence of an equatorial migratory mid-line is a consequence of apoptosis in a narrow nasal-temporal region, the site where eyelids meet during blinking. Elsevier 2017-09-21 /pmc/articles/PMC5639292/ /pubmed/28943255 http://dx.doi.org/10.1016/j.stemcr.2017.08.015 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Richardson, Alexander Lobo, Erwin P. Delic, Naomi C. Myerscough, Mary R. Lyons, J. Guy Wakefield, Denis Di Girolamo, Nick Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title | Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title_full | Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title_fullStr | Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title_full_unstemmed | Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title_short | Keratin-14-Positive Precursor Cells Spawn a Population of Migratory Corneal Epithelia that Maintain Tissue Mass throughout Life |
title_sort | keratin-14-positive precursor cells spawn a population of migratory corneal epithelia that maintain tissue mass throughout life |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639292/ https://www.ncbi.nlm.nih.gov/pubmed/28943255 http://dx.doi.org/10.1016/j.stemcr.2017.08.015 |
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