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Evaluation of Stem Cell Components in Retrocorneal Membranes

The purpose of this study was to elucidate the origin and cellular composition of retrocorneal membranes (RCMs) associated with chemical burns using immunohistochemical staining for primitive cell markers. Six cases of RCMs were collected during penetrating keratoplasty. We examined RCMs with hemato...

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Autores principales: Lee, Seok Hyun, Kim, Kyoung Woo, Kim, Mi Kyung, Chun, Yeoun Sook, Kim, Jae Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055820/
https://www.ncbi.nlm.nih.gov/pubmed/24932088
http://dx.doi.org/10.3346/jkms.2014.29.6.846
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author Lee, Seok Hyun
Kim, Kyoung Woo
Kim, Mi Kyung
Chun, Yeoun Sook
Kim, Jae Chan
author_facet Lee, Seok Hyun
Kim, Kyoung Woo
Kim, Mi Kyung
Chun, Yeoun Sook
Kim, Jae Chan
author_sort Lee, Seok Hyun
collection PubMed
description The purpose of this study was to elucidate the origin and cellular composition of retrocorneal membranes (RCMs) associated with chemical burns using immunohistochemical staining for primitive cell markers. Six cases of RCMs were collected during penetrating keratoplasty. We examined RCMs with hematoxylin and eosin (H&E), periodic acid-Schiff (PAS) staining and immunohistochemical analysis using monoclonal antibodies against hematopoietic stem cells (CD34, CD133, c-kit), mesenchymal stem cells (beta-1-integrin, TGF-β, vimentin, hSTRO-1), fibroblasts (FGF-β, α-smooth muscle actin), and corneal endothelial cells (type IV collagen, CD133, VEGF, VEGFR1). Histologic analysis of RCMs revealed an organized assembly of spindle-shaped cells, pigment-laden cells, and thin collagenous matrix structures. RCMs were positive for markers of mesenchymal stem cells including beta-1-integrin, TGF-β, vimentin, and hSTRO-1. Fibroblast markers were also positive, including FGF-β and α-smooth muscle actin (SMA). In contrast, immunohistochemical staining was negative for hematopoietic stem cell markers including CD34, CD133 and c-kit as well as corneal endothelial cell markers such as type IV collagen, CD133 except VEGF and VEGFR1. Pigment-laden cells did not stain with any antibodies. The results of this study suggest that RCMs consist of a thin collagen matrix and fibroblast-like cells and may be a possible neogenetic structure produced from a lineage of bone marrow-derived mesenchymal stem cells. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-40558202014-06-15 Evaluation of Stem Cell Components in Retrocorneal Membranes Lee, Seok Hyun Kim, Kyoung Woo Kim, Mi Kyung Chun, Yeoun Sook Kim, Jae Chan J Korean Med Sci Original Article The purpose of this study was to elucidate the origin and cellular composition of retrocorneal membranes (RCMs) associated with chemical burns using immunohistochemical staining for primitive cell markers. Six cases of RCMs were collected during penetrating keratoplasty. We examined RCMs with hematoxylin and eosin (H&E), periodic acid-Schiff (PAS) staining and immunohistochemical analysis using monoclonal antibodies against hematopoietic stem cells (CD34, CD133, c-kit), mesenchymal stem cells (beta-1-integrin, TGF-β, vimentin, hSTRO-1), fibroblasts (FGF-β, α-smooth muscle actin), and corneal endothelial cells (type IV collagen, CD133, VEGF, VEGFR1). Histologic analysis of RCMs revealed an organized assembly of spindle-shaped cells, pigment-laden cells, and thin collagenous matrix structures. RCMs were positive for markers of mesenchymal stem cells including beta-1-integrin, TGF-β, vimentin, and hSTRO-1. Fibroblast markers were also positive, including FGF-β and α-smooth muscle actin (SMA). In contrast, immunohistochemical staining was negative for hematopoietic stem cell markers including CD34, CD133 and c-kit as well as corneal endothelial cell markers such as type IV collagen, CD133 except VEGF and VEGFR1. Pigment-laden cells did not stain with any antibodies. The results of this study suggest that RCMs consist of a thin collagen matrix and fibroblast-like cells and may be a possible neogenetic structure produced from a lineage of bone marrow-derived mesenchymal stem cells. GRAPHICAL ABSTRACT: [Image: see text] The Korean Academy of Medical Sciences 2014-06 2014-05-30 /pmc/articles/PMC4055820/ /pubmed/24932088 http://dx.doi.org/10.3346/jkms.2014.29.6.846 Text en © 2014 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Seok Hyun
Kim, Kyoung Woo
Kim, Mi Kyung
Chun, Yeoun Sook
Kim, Jae Chan
Evaluation of Stem Cell Components in Retrocorneal Membranes
title Evaluation of Stem Cell Components in Retrocorneal Membranes
title_full Evaluation of Stem Cell Components in Retrocorneal Membranes
title_fullStr Evaluation of Stem Cell Components in Retrocorneal Membranes
title_full_unstemmed Evaluation of Stem Cell Components in Retrocorneal Membranes
title_short Evaluation of Stem Cell Components in Retrocorneal Membranes
title_sort evaluation of stem cell components in retrocorneal membranes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055820/
https://www.ncbi.nlm.nih.gov/pubmed/24932088
http://dx.doi.org/10.3346/jkms.2014.29.6.846
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