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MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment
BACKGROUND: Fungal Keratitis (FK) is an infective keratopathy with extremely high blindness rate. The damaging effect of this disease is not only the destruction of corneal tissue during fungal infection, but also the cornea scar formed during the healing period after infection control, which can al...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857224/ https://www.ncbi.nlm.nih.gov/pubmed/31727008 http://dx.doi.org/10.1186/s12886-019-1235-6 |
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author | Zhou, Yue Chen, Yuqing Wang, Suiyue Qin, Fangyuan Wang, Liya |
author_facet | Zhou, Yue Chen, Yuqing Wang, Suiyue Qin, Fangyuan Wang, Liya |
author_sort | Zhou, Yue |
collection | PubMed |
description | BACKGROUND: Fungal Keratitis (FK) is an infective keratopathy with extremely high blindness rate. The damaging effect of this disease is not only the destruction of corneal tissue during fungal infection, but also the cornea scar formed during the healing period after infection control, which can also seriously affect a patient’s vision. The purpose of the study was to observe the effect of umbilical cord mesenchymal stem cells (uMSCs) on corneal scar formation in FK. METHODS: The FK mouse model was made according to a previously reported method. Natamycin eye drops were used for antifungal treatment 24 h after modeling. There are four groups involved in the study, including control group, FK group, vehicle(inj) FK group and uMSCs(inj) FK group. Mice in uMSCs(inj) FK group received repeated subconjunctival injections of uMSCs for 3 times at the 1d, 4d and 7d after FK modeling. At 14d, 21d and 28d after trauma, clinical observation, histological examination, second harmonic generation and molecular assays were performed. RESULTS: The uMSCs topical administration reduced corneal scar formation area and corneal opacity, accompanying with decreased corneal thickness and inflammatory cell infiltration, following down-regulated fibrotic-related factors α-SMA, TGFβ1, CTGF, and COLI and finally inhibited phosphorylation of TGFβ1/Smad2 signaling pathway during FK corneal fibrosis. CONCLUSION: The results confirmed that uMSCs can improve corneal opacity during the scar formation stage of FK, and exert anti-inflammatory and anti-fibrotic effects. |
format | Online Article Text |
id | pubmed-6857224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68572242019-12-05 MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment Zhou, Yue Chen, Yuqing Wang, Suiyue Qin, Fangyuan Wang, Liya BMC Ophthalmol Research Article BACKGROUND: Fungal Keratitis (FK) is an infective keratopathy with extremely high blindness rate. The damaging effect of this disease is not only the destruction of corneal tissue during fungal infection, but also the cornea scar formed during the healing period after infection control, which can also seriously affect a patient’s vision. The purpose of the study was to observe the effect of umbilical cord mesenchymal stem cells (uMSCs) on corneal scar formation in FK. METHODS: The FK mouse model was made according to a previously reported method. Natamycin eye drops were used for antifungal treatment 24 h after modeling. There are four groups involved in the study, including control group, FK group, vehicle(inj) FK group and uMSCs(inj) FK group. Mice in uMSCs(inj) FK group received repeated subconjunctival injections of uMSCs for 3 times at the 1d, 4d and 7d after FK modeling. At 14d, 21d and 28d after trauma, clinical observation, histological examination, second harmonic generation and molecular assays were performed. RESULTS: The uMSCs topical administration reduced corneal scar formation area and corneal opacity, accompanying with decreased corneal thickness and inflammatory cell infiltration, following down-regulated fibrotic-related factors α-SMA, TGFβ1, CTGF, and COLI and finally inhibited phosphorylation of TGFβ1/Smad2 signaling pathway during FK corneal fibrosis. CONCLUSION: The results confirmed that uMSCs can improve corneal opacity during the scar formation stage of FK, and exert anti-inflammatory and anti-fibrotic effects. BioMed Central 2019-11-14 /pmc/articles/PMC6857224/ /pubmed/31727008 http://dx.doi.org/10.1186/s12886-019-1235-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhou, Yue Chen, Yuqing Wang, Suiyue Qin, Fangyuan Wang, Liya MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title | MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title_full | MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title_fullStr | MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title_full_unstemmed | MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title_short | MSCs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
title_sort | mscs helped reduce scarring in the cornea after fungal infection when combined with anti-fungal treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857224/ https://www.ncbi.nlm.nih.gov/pubmed/31727008 http://dx.doi.org/10.1186/s12886-019-1235-6 |
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