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Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury
Corneal blindness due to scarring is conventionally treated by corneal transplantation, but the shortage of donor materials has been a major issue affecting the global success of treatment. Pre-clinical and clinical studies have shown that cell-based therapies using either corneal stromal stem cells...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267074/ https://www.ncbi.nlm.nih.gov/pubmed/35805991 http://dx.doi.org/10.3390/ijms23136980 |
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author | Jhanji, Vishal Santra, Mithun Riau, Andri K. Geary, Moira L. Yang, Tianbing Rubin, Elizabeth Yusoff, Nur Zahirah Binte M. Dhaliwal, Deepinder K. Mehta, Jodhbir S. Yam, Gary Hin-Fai |
author_facet | Jhanji, Vishal Santra, Mithun Riau, Andri K. Geary, Moira L. Yang, Tianbing Rubin, Elizabeth Yusoff, Nur Zahirah Binte M. Dhaliwal, Deepinder K. Mehta, Jodhbir S. Yam, Gary Hin-Fai |
author_sort | Jhanji, Vishal |
collection | PubMed |
description | Corneal blindness due to scarring is conventionally treated by corneal transplantation, but the shortage of donor materials has been a major issue affecting the global success of treatment. Pre-clinical and clinical studies have shown that cell-based therapies using either corneal stromal stem cells (CSSC) or corneal stromal keratocytes (CSK) suppress corneal scarring at lower levels. Further treatments or strategies are required to improve the treatment efficacy. This study examined a combined cell-based treatment using CSSC and CSK in a mouse model of anterior stromal injury. We hypothesize that the immuno-regulatory nature of CSSC is effective to control tissue inflammation and delay the onset of fibrosis, and a subsequent intrastromal CSK treatment deposited collagens and stromal specific proteoglycans to recover a native stromal matrix. Using optimized cell doses, our results showed that the effect of CSSC treatment for suppressing corneal opacities was augmented by an additional intrastromal CSK injection, resulting in better corneal clarity. These in vivo effects were substantiated by a further downregulated expression of stromal fibrosis genes and the restoration of stromal fibrillar organization and regularity. Hence, a combined treatment of CSSC and CSK could achieve a higher clinical efficacy and restore corneal transparency, when compared to a single CSSC treatment. |
format | Online Article Text |
id | pubmed-9267074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92670742022-07-09 Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury Jhanji, Vishal Santra, Mithun Riau, Andri K. Geary, Moira L. Yang, Tianbing Rubin, Elizabeth Yusoff, Nur Zahirah Binte M. Dhaliwal, Deepinder K. Mehta, Jodhbir S. Yam, Gary Hin-Fai Int J Mol Sci Article Corneal blindness due to scarring is conventionally treated by corneal transplantation, but the shortage of donor materials has been a major issue affecting the global success of treatment. Pre-clinical and clinical studies have shown that cell-based therapies using either corneal stromal stem cells (CSSC) or corneal stromal keratocytes (CSK) suppress corneal scarring at lower levels. Further treatments or strategies are required to improve the treatment efficacy. This study examined a combined cell-based treatment using CSSC and CSK in a mouse model of anterior stromal injury. We hypothesize that the immuno-regulatory nature of CSSC is effective to control tissue inflammation and delay the onset of fibrosis, and a subsequent intrastromal CSK treatment deposited collagens and stromal specific proteoglycans to recover a native stromal matrix. Using optimized cell doses, our results showed that the effect of CSSC treatment for suppressing corneal opacities was augmented by an additional intrastromal CSK injection, resulting in better corneal clarity. These in vivo effects were substantiated by a further downregulated expression of stromal fibrosis genes and the restoration of stromal fibrillar organization and regularity. Hence, a combined treatment of CSSC and CSK could achieve a higher clinical efficacy and restore corneal transparency, when compared to a single CSSC treatment. MDPI 2022-06-23 /pmc/articles/PMC9267074/ /pubmed/35805991 http://dx.doi.org/10.3390/ijms23136980 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jhanji, Vishal Santra, Mithun Riau, Andri K. Geary, Moira L. Yang, Tianbing Rubin, Elizabeth Yusoff, Nur Zahirah Binte M. Dhaliwal, Deepinder K. Mehta, Jodhbir S. Yam, Gary Hin-Fai Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title | Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title_full | Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title_fullStr | Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title_full_unstemmed | Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title_short | Combined Therapy Using Human Corneal Stromal Stem Cells and Quiescent Keratocytes to Prevent Corneal Scarring after Injury |
title_sort | combined therapy using human corneal stromal stem cells and quiescent keratocytes to prevent corneal scarring after injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267074/ https://www.ncbi.nlm.nih.gov/pubmed/35805991 http://dx.doi.org/10.3390/ijms23136980 |
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