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Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes
Cellular factor XIII (cFXIII, FXIII-A(2)), a transglutaminase, has been demonstrated in a few cell types. Its main function is to cross-link proteins by isopeptide bonds. Here, we investigated the presence of cFXIII in cells of human cornea. Tissue sections of the cornea were immunostained for FXIII...
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/PMC6928837/ https://www.ncbi.nlm.nih.gov/pubmed/31783511 http://dx.doi.org/10.3390/ijms20235963 |
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author | Orosz, Zsuzsanna Z. Bárdos, Helga Shemirani, Amir H. Beke Debreceni, Ildikó Lassila, Riitta Riikonen, Antti S. Kremer Hovinga, Johanna A. Seiler, Theo G. van Dorland, Hendrika A. Schroeder, Verena Boda, Zoltán Nemes, László Früh Eppstein, Beatrice Nagy, Bence Facskó, Andrea Kappelmayer, János Muszbek, László |
author_facet | Orosz, Zsuzsanna Z. Bárdos, Helga Shemirani, Amir H. Beke Debreceni, Ildikó Lassila, Riitta Riikonen, Antti S. Kremer Hovinga, Johanna A. Seiler, Theo G. van Dorland, Hendrika A. Schroeder, Verena Boda, Zoltán Nemes, László Früh Eppstein, Beatrice Nagy, Bence Facskó, Andrea Kappelmayer, János Muszbek, László |
author_sort | Orosz, Zsuzsanna Z. |
collection | PubMed |
description | Cellular factor XIII (cFXIII, FXIII-A(2)), a transglutaminase, has been demonstrated in a few cell types. Its main function is to cross-link proteins by isopeptide bonds. Here, we investigated the presence of cFXIII in cells of human cornea. Tissue sections of the cornea were immunostained for FXIII-A in combination with staining for CD34 antigen or isopeptide cross-links. Isolated corneal keratocytes were also evaluated by immunofluorescent microscopy and flow cytometry. FXIII-A in the corneal stroma was quantified by Western blotting. FXIII-A mRNA was detected by RT-qPCR. The cornea of FXIII-A-deficient patients was evaluated by cornea topography. FXIII-A was detected in 68 ± 13% of CD34+ keratocytes. Their distribution in the corneal stroma was unequal; they were most abundant in the subepithelial tertile. cFXIII was of cytoplasmic localization. In the stroma, 3.64 ng cFXIII/mg protein was measured. The synthesis of cFXIII by keratocytes was confirmed by RT-qPCR. Isopeptide cross-links were detected above, but not within the corneal stroma. Slight abnormality of the cornea was detected in six out of nine FXIII-A-deficient patients. The presence of cFXIII in human keratocytes was established for the first time. cFXIII might be involved in maintaining the stability of the cornea and in the corneal wound healing process. |
format | Online Article Text |
id | pubmed-6928837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69288372019-12-26 Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes Orosz, Zsuzsanna Z. Bárdos, Helga Shemirani, Amir H. Beke Debreceni, Ildikó Lassila, Riitta Riikonen, Antti S. Kremer Hovinga, Johanna A. Seiler, Theo G. van Dorland, Hendrika A. Schroeder, Verena Boda, Zoltán Nemes, László Früh Eppstein, Beatrice Nagy, Bence Facskó, Andrea Kappelmayer, János Muszbek, László Int J Mol Sci Article Cellular factor XIII (cFXIII, FXIII-A(2)), a transglutaminase, has been demonstrated in a few cell types. Its main function is to cross-link proteins by isopeptide bonds. Here, we investigated the presence of cFXIII in cells of human cornea. Tissue sections of the cornea were immunostained for FXIII-A in combination with staining for CD34 antigen or isopeptide cross-links. Isolated corneal keratocytes were also evaluated by immunofluorescent microscopy and flow cytometry. FXIII-A in the corneal stroma was quantified by Western blotting. FXIII-A mRNA was detected by RT-qPCR. The cornea of FXIII-A-deficient patients was evaluated by cornea topography. FXIII-A was detected in 68 ± 13% of CD34+ keratocytes. Their distribution in the corneal stroma was unequal; they were most abundant in the subepithelial tertile. cFXIII was of cytoplasmic localization. In the stroma, 3.64 ng cFXIII/mg protein was measured. The synthesis of cFXIII by keratocytes was confirmed by RT-qPCR. Isopeptide cross-links were detected above, but not within the corneal stroma. Slight abnormality of the cornea was detected in six out of nine FXIII-A-deficient patients. The presence of cFXIII in human keratocytes was established for the first time. cFXIII might be involved in maintaining the stability of the cornea and in the corneal wound healing process. MDPI 2019-11-27 /pmc/articles/PMC6928837/ /pubmed/31783511 http://dx.doi.org/10.3390/ijms20235963 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 Orosz, Zsuzsanna Z. Bárdos, Helga Shemirani, Amir H. Beke Debreceni, Ildikó Lassila, Riitta Riikonen, Antti S. Kremer Hovinga, Johanna A. Seiler, Theo G. van Dorland, Hendrika A. Schroeder, Verena Boda, Zoltán Nemes, László Früh Eppstein, Beatrice Nagy, Bence Facskó, Andrea Kappelmayer, János Muszbek, László Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title | Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title_full | Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title_fullStr | Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title_full_unstemmed | Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title_short | Cellular Factor XIII, a Transglutaminase in Human Corneal Keratocytes |
title_sort | cellular factor xiii, a transglutaminase in human corneal keratocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928837/ https://www.ncbi.nlm.nih.gov/pubmed/31783511 http://dx.doi.org/10.3390/ijms20235963 |
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