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Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium
The corneal endothelium regulates corneal hydration to maintain the transparency of cornea. Lacking regenerative capacity, corneal endothelial cell loss due to aging and diseases can lead to corneal edema and vision loss. There is limited information on the existence of corneal endothelial progenito...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829622/ https://www.ncbi.nlm.nih.gov/pubmed/31614883 http://dx.doi.org/10.3390/cells8101244 |
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author | Yam, Gary Hin-Fai Seah, Xinyi Yusoff, Nur Zahirah Binte M Setiawan, Melina Wahlig, Stephen Htoon, Hla Myint Peh, Gary S.L. Kocaba, Viridiana Mehta, Jodhbir S |
author_facet | Yam, Gary Hin-Fai Seah, Xinyi Yusoff, Nur Zahirah Binte M Setiawan, Melina Wahlig, Stephen Htoon, Hla Myint Peh, Gary S.L. Kocaba, Viridiana Mehta, Jodhbir S |
author_sort | Yam, Gary Hin-Fai |
collection | PubMed |
description | The corneal endothelium regulates corneal hydration to maintain the transparency of cornea. Lacking regenerative capacity, corneal endothelial cell loss due to aging and diseases can lead to corneal edema and vision loss. There is limited information on the existence of corneal endothelial progenitors. We conducted ultrastructural examinations and expression analyses on the human transition zone (TZ) at the posterior limbus of corneal periphery, to elucidate if the TZ harbored progenitor-like cells, and to reveal their niche characteristics. Within the narrow TZ (~190 μm width), the inner TZ—adjacent to the peripheral endothelium (PE)—contained cells expressing stem/progenitor markers (Sox2, Lgr5, CD34, Pitx2, telomerase). They were located on the inner TZ surface and in its underlying stroma. Lgr5 positive cells projected as multicellular clusters into the PE. Under transmission electron microscopy and serial block face-scanning electron microscopy and three-dimensional (3D) reconstruction, the terminal margin of Descemet’s membrane was inserted beneath the TZ surface, with the distance akin to the inner TZ breadth. Porcine TZ cells were isolated and proliferated into a confluent monolayer and differentiated to cells expressing corneal endothelial markers (ZO1, Na(+)K(+)ATPase) on cell surface. In conclusion, we have identified a novel inner TZ containing progenitor-like cells, which could serve the regenerative potential for corneal endothelium. |
format | Online Article Text |
id | pubmed-6829622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68296222019-11-18 Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium Yam, Gary Hin-Fai Seah, Xinyi Yusoff, Nur Zahirah Binte M Setiawan, Melina Wahlig, Stephen Htoon, Hla Myint Peh, Gary S.L. Kocaba, Viridiana Mehta, Jodhbir S Cells Article The corneal endothelium regulates corneal hydration to maintain the transparency of cornea. Lacking regenerative capacity, corneal endothelial cell loss due to aging and diseases can lead to corneal edema and vision loss. There is limited information on the existence of corneal endothelial progenitors. We conducted ultrastructural examinations and expression analyses on the human transition zone (TZ) at the posterior limbus of corneal periphery, to elucidate if the TZ harbored progenitor-like cells, and to reveal their niche characteristics. Within the narrow TZ (~190 μm width), the inner TZ—adjacent to the peripheral endothelium (PE)—contained cells expressing stem/progenitor markers (Sox2, Lgr5, CD34, Pitx2, telomerase). They were located on the inner TZ surface and in its underlying stroma. Lgr5 positive cells projected as multicellular clusters into the PE. Under transmission electron microscopy and serial block face-scanning electron microscopy and three-dimensional (3D) reconstruction, the terminal margin of Descemet’s membrane was inserted beneath the TZ surface, with the distance akin to the inner TZ breadth. Porcine TZ cells were isolated and proliferated into a confluent monolayer and differentiated to cells expressing corneal endothelial markers (ZO1, Na(+)K(+)ATPase) on cell surface. In conclusion, we have identified a novel inner TZ containing progenitor-like cells, which could serve the regenerative potential for corneal endothelium. MDPI 2019-10-12 /pmc/articles/PMC6829622/ /pubmed/31614883 http://dx.doi.org/10.3390/cells8101244 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yam, Gary Hin-Fai Seah, Xinyi Yusoff, Nur Zahirah Binte M Setiawan, Melina Wahlig, Stephen Htoon, Hla Myint Peh, Gary S.L. Kocaba, Viridiana Mehta, Jodhbir S Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title | Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title_full | Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title_fullStr | Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title_full_unstemmed | Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title_short | Characterization of Human Transition Zone Reveals a Putative Progenitor-Enriched Niche of Corneal Endothelium |
title_sort | characterization of human transition zone reveals a putative progenitor-enriched niche of corneal endothelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829622/ https://www.ncbi.nlm.nih.gov/pubmed/31614883 http://dx.doi.org/10.3390/cells8101244 |
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