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Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction
BACKGROUND: Corneal transplantation is the only way to treat serious corneal diseases caused by corneal endothelial dysfunction. However, the shortage of donor corneal tissues and human corneal endothelial cells (HCECs) remains a worldwide challenge. We cultivated HCECs by the use of a conditioned m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166479/ https://www.ncbi.nlm.nih.gov/pubmed/35659288 http://dx.doi.org/10.1186/s13287-022-02889-x |
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author | Sun, Peng Shen, Lin Li, Yuan-Bin Du, Li-Qun Wu, Xin-Yi |
author_facet | Sun, Peng Shen, Lin Li, Yuan-Bin Du, Li-Qun Wu, Xin-Yi |
author_sort | Sun, Peng |
collection | PubMed |
description | BACKGROUND: Corneal transplantation is the only way to treat serious corneal diseases caused by corneal endothelial dysfunction. However, the shortage of donor corneal tissues and human corneal endothelial cells (HCECs) remains a worldwide challenge. We cultivated HCECs by the use of a conditioned medium from orbital adipose-derived stem cells (OASC-CM) in vitro. Then the HCECs were used to treat animal corneal endothelial dysfunction models via cell transplantation. The purpose of this study was to conduct a long-term observation and evaluation after cell transplantation. METHODS: Orbital adipose-derived stem cells (OASCs) were isolated to prepare the conditioned medium (CM). HCECs were cultivated and expanded by the usage of the CM (CM-HCECs). Then, related corneal endothelial cell (CEC) markers were analyzed by immunofluorescence. The cell proliferation ability was also tested. CM-HCECs were then transplanted into monkey corneal endothelial dysfunction models by injection. We carried out a 24-month postoperative preclinical observation and verified the long-term effect by histological examination and transcriptome sequencing. RESULTS: CM-HCECs strongly expressed CEC-related markers and maintained polygonal cell morphology even after 10 passages. At 24 months after cell transplantation, there was a CEC density of more than 2400 cells per square millimeter (range, 2408–2685) in the experimental group. A corneal thickness (CT) of less than 550 μm (range, 490–510) was attained. Gene sequencing showed that the gene expression pattern of CM-HCECs was similar to that of transplanted cells and HCECs. CONCLUSIONS: Transplantation of CM-HCECs into monkey corneal endothelial dysfunction models resulted in a transparent cornea after 24 months. This research provided a promising prospect of cell-based therapy for corneal endothelial diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02889-x. |
format | Online Article Text |
id | pubmed-9166479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91664792022-06-05 Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction Sun, Peng Shen, Lin Li, Yuan-Bin Du, Li-Qun Wu, Xin-Yi Stem Cell Res Ther Research BACKGROUND: Corneal transplantation is the only way to treat serious corneal diseases caused by corneal endothelial dysfunction. However, the shortage of donor corneal tissues and human corneal endothelial cells (HCECs) remains a worldwide challenge. We cultivated HCECs by the use of a conditioned medium from orbital adipose-derived stem cells (OASC-CM) in vitro. Then the HCECs were used to treat animal corneal endothelial dysfunction models via cell transplantation. The purpose of this study was to conduct a long-term observation and evaluation after cell transplantation. METHODS: Orbital adipose-derived stem cells (OASCs) were isolated to prepare the conditioned medium (CM). HCECs were cultivated and expanded by the usage of the CM (CM-HCECs). Then, related corneal endothelial cell (CEC) markers were analyzed by immunofluorescence. The cell proliferation ability was also tested. CM-HCECs were then transplanted into monkey corneal endothelial dysfunction models by injection. We carried out a 24-month postoperative preclinical observation and verified the long-term effect by histological examination and transcriptome sequencing. RESULTS: CM-HCECs strongly expressed CEC-related markers and maintained polygonal cell morphology even after 10 passages. At 24 months after cell transplantation, there was a CEC density of more than 2400 cells per square millimeter (range, 2408–2685) in the experimental group. A corneal thickness (CT) of less than 550 μm (range, 490–510) was attained. Gene sequencing showed that the gene expression pattern of CM-HCECs was similar to that of transplanted cells and HCECs. CONCLUSIONS: Transplantation of CM-HCECs into monkey corneal endothelial dysfunction models resulted in a transparent cornea after 24 months. This research provided a promising prospect of cell-based therapy for corneal endothelial diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02889-x. BioMed Central 2022-06-03 /pmc/articles/PMC9166479/ /pubmed/35659288 http://dx.doi.org/10.1186/s13287-022-02889-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sun, Peng Shen, Lin Li, Yuan-Bin Du, Li-Qun Wu, Xin-Yi Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title | Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title_full | Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title_fullStr | Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title_full_unstemmed | Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title_short | Long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
title_sort | long-term observation after transplantation of cultured human corneal endothelial cells for corneal endothelial dysfunction |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166479/ https://www.ncbi.nlm.nih.gov/pubmed/35659288 http://dx.doi.org/10.1186/s13287-022-02889-x |
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