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Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography

Diagnosis of corneal disease and challenges in corneal transplantation require comprehensive understanding of corneal anatomy, particularly that of the posterior cornea. Micro-optical coherence tomography (µOCT) is a potentially suitable tool to meet this need, owing to its ultrahigh isotropic spati...

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Autores principales: Chen, Si, Liu, Xinyu, Wang, Nanshuo, Wang, Xianghong, Xiong, Qiaozhou, Bo, En, Yu, Xiaojun, Chen, Shufen, Liu, Linbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589810/
https://www.ncbi.nlm.nih.gov/pubmed/28883661
http://dx.doi.org/10.1038/s41598-017-11380-0
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author Chen, Si
Liu, Xinyu
Wang, Nanshuo
Wang, Xianghong
Xiong, Qiaozhou
Bo, En
Yu, Xiaojun
Chen, Shufen
Liu, Linbo
author_facet Chen, Si
Liu, Xinyu
Wang, Nanshuo
Wang, Xianghong
Xiong, Qiaozhou
Bo, En
Yu, Xiaojun
Chen, Shufen
Liu, Linbo
author_sort Chen, Si
collection PubMed
description Diagnosis of corneal disease and challenges in corneal transplantation require comprehensive understanding of corneal anatomy, particularly that of the posterior cornea. Micro-optical coherence tomography (µOCT) is a potentially suitable tool to meet this need, owing to its ultrahigh isotropic spatial resolution, high image acquisition rate and depth priority scanning mode. In this study, we explored the ability of µOCT to visualize micro-anatomical structures of the posterior cornea ex vivo and in vivo using small and large animals. µOCT clearly delineated cornea layers and revealed micro-anatomical structures, including not only polygonal endothelial cells, stellate keratocytes, collagen fibres and corneal nerve fibres but also new structures such as the dome-shaped basolateral side of endothelial cells and lattice structures at the interface between endothelium and Descemet’s membrane. Based on these observations, a short post-harvest longitudinal study was conducted on rat cornea to test the feasibility of using µOCT to monitor the quality of endothelial cells. This study successfully reveals a series of morphological features and pathological changes in the posterior cornea at the cellular level in situ and in real time with µOCT. These findings enrich knowledge of corneal anatomy and suggest that µOCT may be a promising imaging tool in corneal transplantation.
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spelling pubmed-55898102017-09-13 Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography Chen, Si Liu, Xinyu Wang, Nanshuo Wang, Xianghong Xiong, Qiaozhou Bo, En Yu, Xiaojun Chen, Shufen Liu, Linbo Sci Rep Article Diagnosis of corneal disease and challenges in corneal transplantation require comprehensive understanding of corneal anatomy, particularly that of the posterior cornea. Micro-optical coherence tomography (µOCT) is a potentially suitable tool to meet this need, owing to its ultrahigh isotropic spatial resolution, high image acquisition rate and depth priority scanning mode. In this study, we explored the ability of µOCT to visualize micro-anatomical structures of the posterior cornea ex vivo and in vivo using small and large animals. µOCT clearly delineated cornea layers and revealed micro-anatomical structures, including not only polygonal endothelial cells, stellate keratocytes, collagen fibres and corneal nerve fibres but also new structures such as the dome-shaped basolateral side of endothelial cells and lattice structures at the interface between endothelium and Descemet’s membrane. Based on these observations, a short post-harvest longitudinal study was conducted on rat cornea to test the feasibility of using µOCT to monitor the quality of endothelial cells. This study successfully reveals a series of morphological features and pathological changes in the posterior cornea at the cellular level in situ and in real time with µOCT. These findings enrich knowledge of corneal anatomy and suggest that µOCT may be a promising imaging tool in corneal transplantation. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589810/ /pubmed/28883661 http://dx.doi.org/10.1038/s41598-017-11380-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Si
Liu, Xinyu
Wang, Nanshuo
Wang, Xianghong
Xiong, Qiaozhou
Bo, En
Yu, Xiaojun
Chen, Shufen
Liu, Linbo
Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title_full Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title_fullStr Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title_full_unstemmed Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title_short Visualizing Micro-anatomical Structures of the Posterior Cornea with Micro-optical Coherence Tomography
title_sort visualizing micro-anatomical structures of the posterior cornea with micro-optical coherence tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589810/
https://www.ncbi.nlm.nih.gov/pubmed/28883661
http://dx.doi.org/10.1038/s41598-017-11380-0
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