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Cell maturation influences the ability of hESC-RPE to tolerate cellular stress
BACKGROUND: Transplantation of human pluripotent stem cell-derived retinal pigment epithelium (RPE) is an urgently needed treatment for the cure of degenerative diseases of the retina. The transplanted cells must tolerate cellular stress caused by various sources such as retinal inflammation and reg...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785579/ https://www.ncbi.nlm.nih.gov/pubmed/35073969 http://dx.doi.org/10.1186/s13287-022-02712-7 |
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author | Viheriälä, Taina Hongisto, Heidi Sorvari, Juhana Skottman, Heli Nymark, Soile Ilmarinen, Tanja |
author_facet | Viheriälä, Taina Hongisto, Heidi Sorvari, Juhana Skottman, Heli Nymark, Soile Ilmarinen, Tanja |
author_sort | Viheriälä, Taina |
collection | PubMed |
description | BACKGROUND: Transplantation of human pluripotent stem cell-derived retinal pigment epithelium (RPE) is an urgently needed treatment for the cure of degenerative diseases of the retina. The transplanted cells must tolerate cellular stress caused by various sources such as retinal inflammation and regain their functions rapidly after the transplantation. We have previously shown the maturation level of the cultured human embryonic stem cell-derived RPE (hESC-RPE) cells to influence for example their calcium (Ca(2+)) signaling properties. Yet, no comparison of the ability of hESC-RPE at different maturity levels to tolerate cellular stress has been reported. METHODS: Here, we analyzed the ability of the hESC-RPE populations with early (3 weeks) and late (12 weeks) maturation status to tolerate cellular stress caused by chemical cell stressors protease inhibitor (MG132) or hydrogen peroxide (H(2)O(2)). After the treatments, the functionality of the RPE cells was studied by transepithelial resistance, immunostainings of key RPE proteins, phagocytosis, mitochondrial membrane potential, Ca(2+) signaling, and cytokine secretion. RESULTS: The hESC-RPE population with late maturation status consistently showed improved tolerance to cellular stress in comparison to the population with early maturity. After the treatments, the early maturation status of hESC-RPE monolayer showed impaired barrier properties. The hESC-RPE with early maturity status also exhibited reduced phagocytic and Ca(2+) signaling properties, especially after MG132 treatment. CONCLUSIONS: Our results suggest that due to better tolerance to cellular stress, the late maturation status of hESC-RPE population is superior compared to monolayers with early maturation status in the transplantation therapy settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02712-7. |
format | Online Article Text |
id | pubmed-8785579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87855792022-01-24 Cell maturation influences the ability of hESC-RPE to tolerate cellular stress Viheriälä, Taina Hongisto, Heidi Sorvari, Juhana Skottman, Heli Nymark, Soile Ilmarinen, Tanja Stem Cell Res Ther Research BACKGROUND: Transplantation of human pluripotent stem cell-derived retinal pigment epithelium (RPE) is an urgently needed treatment for the cure of degenerative diseases of the retina. The transplanted cells must tolerate cellular stress caused by various sources such as retinal inflammation and regain their functions rapidly after the transplantation. We have previously shown the maturation level of the cultured human embryonic stem cell-derived RPE (hESC-RPE) cells to influence for example their calcium (Ca(2+)) signaling properties. Yet, no comparison of the ability of hESC-RPE at different maturity levels to tolerate cellular stress has been reported. METHODS: Here, we analyzed the ability of the hESC-RPE populations with early (3 weeks) and late (12 weeks) maturation status to tolerate cellular stress caused by chemical cell stressors protease inhibitor (MG132) or hydrogen peroxide (H(2)O(2)). After the treatments, the functionality of the RPE cells was studied by transepithelial resistance, immunostainings of key RPE proteins, phagocytosis, mitochondrial membrane potential, Ca(2+) signaling, and cytokine secretion. RESULTS: The hESC-RPE population with late maturation status consistently showed improved tolerance to cellular stress in comparison to the population with early maturity. After the treatments, the early maturation status of hESC-RPE monolayer showed impaired barrier properties. The hESC-RPE with early maturity status also exhibited reduced phagocytic and Ca(2+) signaling properties, especially after MG132 treatment. CONCLUSIONS: Our results suggest that due to better tolerance to cellular stress, the late maturation status of hESC-RPE population is superior compared to monolayers with early maturation status in the transplantation therapy settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02712-7. BioMed Central 2022-01-24 /pmc/articles/PMC8785579/ /pubmed/35073969 http://dx.doi.org/10.1186/s13287-022-02712-7 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 Viheriälä, Taina Hongisto, Heidi Sorvari, Juhana Skottman, Heli Nymark, Soile Ilmarinen, Tanja Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title | Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title_full | Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title_fullStr | Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title_full_unstemmed | Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title_short | Cell maturation influences the ability of hESC-RPE to tolerate cellular stress |
title_sort | cell maturation influences the ability of hesc-rpe to tolerate cellular stress |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8785579/ https://www.ncbi.nlm.nih.gov/pubmed/35073969 http://dx.doi.org/10.1186/s13287-022-02712-7 |
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