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In vivo fluorescence imaging of conjunctival goblet cells

Conjunctival goblet cells (GCs) are specialized epithelial cells that secrete mucins onto the ocular surface to maintain the wet environment. Assessment of GCs is important because various ocular surface diseases are associated with their loss. Although there are GC assessment methods available, the...

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Autores principales: Kim, Seonghan, Lee, Seunghun, Chang, Hoonchul, Kim, Moses, Kim, Myoung Joon, Kim, Ki Hean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820527/
https://www.ncbi.nlm.nih.gov/pubmed/31664078
http://dx.doi.org/10.1038/s41598-019-51893-4
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author Kim, Seonghan
Lee, Seunghun
Chang, Hoonchul
Kim, Moses
Kim, Myoung Joon
Kim, Ki Hean
author_facet Kim, Seonghan
Lee, Seunghun
Chang, Hoonchul
Kim, Moses
Kim, Myoung Joon
Kim, Ki Hean
author_sort Kim, Seonghan
collection PubMed
description Conjunctival goblet cells (GCs) are specialized epithelial cells that secrete mucins onto the ocular surface to maintain the wet environment. Assessment of GCs is important because various ocular surface diseases are associated with their loss. Although there are GC assessment methods available, the current methods are either invasive or difficult to use. In this report, we developed a simple and non-invasive GC assessment method based on fluorescence imaging. Moxifloxacin ophthalmic solution was used to label GCs via topical administration, and then various fluorescence microscopies could image GCs in high contrasts. Fluorescence imaging of GCs in the mouse conjunctiva was confirmed by both confocal reflection microscopy and histology with Periodic acid-Schiff (PAS) labeling. Real-time in-vivo conjunctival GC imaging was demonstrated in a rat model by using both confocal fluorescence microscopy and simple wide-field fluorescence microscopy. Different GC densities were observed in the forniceal and bulbar conjunctivas of the rat eye. Moxifloxacin based fluorescence imaging provides high-contrast images of conjunctival GCs non-invasively and could be useful for the study or diagnosis of GC related ocular surface diseases.
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spelling pubmed-68205272019-11-04 In vivo fluorescence imaging of conjunctival goblet cells Kim, Seonghan Lee, Seunghun Chang, Hoonchul Kim, Moses Kim, Myoung Joon Kim, Ki Hean Sci Rep Article Conjunctival goblet cells (GCs) are specialized epithelial cells that secrete mucins onto the ocular surface to maintain the wet environment. Assessment of GCs is important because various ocular surface diseases are associated with their loss. Although there are GC assessment methods available, the current methods are either invasive or difficult to use. In this report, we developed a simple and non-invasive GC assessment method based on fluorescence imaging. Moxifloxacin ophthalmic solution was used to label GCs via topical administration, and then various fluorescence microscopies could image GCs in high contrasts. Fluorescence imaging of GCs in the mouse conjunctiva was confirmed by both confocal reflection microscopy and histology with Periodic acid-Schiff (PAS) labeling. Real-time in-vivo conjunctival GC imaging was demonstrated in a rat model by using both confocal fluorescence microscopy and simple wide-field fluorescence microscopy. Different GC densities were observed in the forniceal and bulbar conjunctivas of the rat eye. Moxifloxacin based fluorescence imaging provides high-contrast images of conjunctival GCs non-invasively and could be useful for the study or diagnosis of GC related ocular surface diseases. Nature Publishing Group UK 2019-10-29 /pmc/articles/PMC6820527/ /pubmed/31664078 http://dx.doi.org/10.1038/s41598-019-51893-4 Text en © The Author(s) 2019 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
Kim, Seonghan
Lee, Seunghun
Chang, Hoonchul
Kim, Moses
Kim, Myoung Joon
Kim, Ki Hean
In vivo fluorescence imaging of conjunctival goblet cells
title In vivo fluorescence imaging of conjunctival goblet cells
title_full In vivo fluorescence imaging of conjunctival goblet cells
title_fullStr In vivo fluorescence imaging of conjunctival goblet cells
title_full_unstemmed In vivo fluorescence imaging of conjunctival goblet cells
title_short In vivo fluorescence imaging of conjunctival goblet cells
title_sort in vivo fluorescence imaging of conjunctival goblet cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820527/
https://www.ncbi.nlm.nih.gov/pubmed/31664078
http://dx.doi.org/10.1038/s41598-019-51893-4
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