Cargando…
Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β
The short supply of donor corneas is exacerbated by the unsuitability of donors with insufficient endothelial cell density. Few studies have investigated promoting corneal endothelial cell proliferation to increase the endothelial cell density. We hypothesize that pre‐transplantation treatment of pr...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299697/ https://www.ncbi.nlm.nih.gov/pubmed/32333497 http://dx.doi.org/10.1111/jcmm.15307 |
_version_ | 1783547442305695744 |
---|---|
author | Hsueh, Yi‐Jen Meir, Yaa‐Jyuhn James Lai, Jui‐Yang Chen, Hung‐Chi Ma, David Hui‐Kang Huang, Chieh‐Cheng Lu, Tsai‐Te Cheng, Chao‐Min Wu, Wei‐Chi |
author_facet | Hsueh, Yi‐Jen Meir, Yaa‐Jyuhn James Lai, Jui‐Yang Chen, Hung‐Chi Ma, David Hui‐Kang Huang, Chieh‐Cheng Lu, Tsai‐Te Cheng, Chao‐Min Wu, Wei‐Chi |
author_sort | Hsueh, Yi‐Jen |
collection | PubMed |
description | The short supply of donor corneas is exacerbated by the unsuitability of donors with insufficient endothelial cell density. Few studies have investigated promoting corneal endothelial cell proliferation to increase the endothelial cell density. We hypothesize that pre‐transplantation treatment of proliferative tissue‐cultivated corneas may increase corneal endothelial cell density. We observed that the airlift cultures were superior to immersion cultures with respect to both transparency and thickness. In this tissue culture system, we observed that lysophosphatidic acid increased the rabbit corneal endothelial cell density, number of BrdU‐positive cells and improve wound healing. We also observed an indirect effect of lysophosphatidic acid on corneal endothelial cell proliferation mediated by the stimulation of interleukin‐1β secretion from stromal cells. Human corneal tissues treated with lysophosphatidic acid or interleukin‐1β contained significantly more Ki‐67‐positive cells than untreated group. The lysophosphatidic acid‐ or interleukin‐1β‐treated cultured tissue remained hexagon‐shaped, with ZO‐1 expression and no evidence of the endothelial‐mesenchymal transition. Our novel protocol of tissue culture may be applicable for eye banks to optimize corneal grafting. |
format | Online Article Text |
id | pubmed-7299697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72996972020-06-18 Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β Hsueh, Yi‐Jen Meir, Yaa‐Jyuhn James Lai, Jui‐Yang Chen, Hung‐Chi Ma, David Hui‐Kang Huang, Chieh‐Cheng Lu, Tsai‐Te Cheng, Chao‐Min Wu, Wei‐Chi J Cell Mol Med Original Articles The short supply of donor corneas is exacerbated by the unsuitability of donors with insufficient endothelial cell density. Few studies have investigated promoting corneal endothelial cell proliferation to increase the endothelial cell density. We hypothesize that pre‐transplantation treatment of proliferative tissue‐cultivated corneas may increase corneal endothelial cell density. We observed that the airlift cultures were superior to immersion cultures with respect to both transparency and thickness. In this tissue culture system, we observed that lysophosphatidic acid increased the rabbit corneal endothelial cell density, number of BrdU‐positive cells and improve wound healing. We also observed an indirect effect of lysophosphatidic acid on corneal endothelial cell proliferation mediated by the stimulation of interleukin‐1β secretion from stromal cells. Human corneal tissues treated with lysophosphatidic acid or interleukin‐1β contained significantly more Ki‐67‐positive cells than untreated group. The lysophosphatidic acid‐ or interleukin‐1β‐treated cultured tissue remained hexagon‐shaped, with ZO‐1 expression and no evidence of the endothelial‐mesenchymal transition. Our novel protocol of tissue culture may be applicable for eye banks to optimize corneal grafting. John Wiley and Sons Inc. 2020-04-24 2020-06 /pmc/articles/PMC7299697/ /pubmed/32333497 http://dx.doi.org/10.1111/jcmm.15307 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hsueh, Yi‐Jen Meir, Yaa‐Jyuhn James Lai, Jui‐Yang Chen, Hung‐Chi Ma, David Hui‐Kang Huang, Chieh‐Cheng Lu, Tsai‐Te Cheng, Chao‐Min Wu, Wei‐Chi Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title | Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title_full | Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title_fullStr | Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title_full_unstemmed | Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title_short | Lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
title_sort | lysophosphatidic acid improves corneal endothelial density in tissue culture by stimulating stromal secretion of interleukin‐1β |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299697/ https://www.ncbi.nlm.nih.gov/pubmed/32333497 http://dx.doi.org/10.1111/jcmm.15307 |
work_keys_str_mv | AT hsuehyijen lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT meiryaajyuhnjames lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT laijuiyang lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT chenhungchi lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT madavidhuikang lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT huangchiehcheng lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT lutsaite lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT chengchaomin lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b AT wuweichi lysophosphatidicacidimprovescornealendothelialdensityintissueculturebystimulatingstromalsecretionofinterleukin1b |