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Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment

Retinal pigment epithelium (RPE) is a specialized structure essential for proper vision, which is constantly exposed to oxidative damage. With aging, this damage accumulates within the RPE cells, causing various diseases, including age-related macular degeneration (AMD). Numerous antioxidant substan...

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Autores principales: Strzalka-Mrozik, Barbara, Madej, Marcel, Kurowska, Natalia, Kruszniewska-Rajs, Celina, Kimsa-Dudek, Magdalena, Adamska, Jolanta, Gola, Joanna Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955508/
https://www.ncbi.nlm.nih.gov/pubmed/36826042
http://dx.doi.org/10.3390/cimb45020097
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author Strzalka-Mrozik, Barbara
Madej, Marcel
Kurowska, Natalia
Kruszniewska-Rajs, Celina
Kimsa-Dudek, Magdalena
Adamska, Jolanta
Gola, Joanna Magdalena
author_facet Strzalka-Mrozik, Barbara
Madej, Marcel
Kurowska, Natalia
Kruszniewska-Rajs, Celina
Kimsa-Dudek, Magdalena
Adamska, Jolanta
Gola, Joanna Magdalena
author_sort Strzalka-Mrozik, Barbara
collection PubMed
description Retinal pigment epithelium (RPE) is a specialized structure essential for proper vision, which is constantly exposed to oxidative damage. With aging, this damage accumulates within the RPE cells, causing various diseases, including age-related macular degeneration (AMD). Numerous antioxidant substances are used to prevent this process in humans, including lutein. This study aims to determine the differences in the expression patterns of pyroptosis genes in senescent human retinal pigment epithelial cell line ARPE-19 exposed to lutein. Changes in the expression of pyroptosis-related genes were assessed by oligonucleotide microarrays, and the results were validated by real-time RT-qPCR. The microarray analysis showed seven transcripts were differentially expressed both in the H(2)O(2)-treated cells versus the controls and in the lutein/H(2)O(2)-treated cells compared to the H(2)O(2)-treated cells (FC > 2.0). Depending on the used lutein, H(2)O(2), or co-treatment of ARPE-19 cells, statistically significant differences in the expression of TXNIP, CXCL8, BAX, and CASP1 genes were confirmed by the RT-qPCR (p < 0.05). A STRING database analysis showed that the proteins encoded by the analyzed genes form a strong interaction network (p < 0.001). These data indicate that lutein modulates the expression level of pyroptosis-related genes, which may be useful for the development of new methods preventing pyroptosis pathway activation in the future.
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spelling pubmed-99555082023-02-25 Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment Strzalka-Mrozik, Barbara Madej, Marcel Kurowska, Natalia Kruszniewska-Rajs, Celina Kimsa-Dudek, Magdalena Adamska, Jolanta Gola, Joanna Magdalena Curr Issues Mol Biol Article Retinal pigment epithelium (RPE) is a specialized structure essential for proper vision, which is constantly exposed to oxidative damage. With aging, this damage accumulates within the RPE cells, causing various diseases, including age-related macular degeneration (AMD). Numerous antioxidant substances are used to prevent this process in humans, including lutein. This study aims to determine the differences in the expression patterns of pyroptosis genes in senescent human retinal pigment epithelial cell line ARPE-19 exposed to lutein. Changes in the expression of pyroptosis-related genes were assessed by oligonucleotide microarrays, and the results were validated by real-time RT-qPCR. The microarray analysis showed seven transcripts were differentially expressed both in the H(2)O(2)-treated cells versus the controls and in the lutein/H(2)O(2)-treated cells compared to the H(2)O(2)-treated cells (FC > 2.0). Depending on the used lutein, H(2)O(2), or co-treatment of ARPE-19 cells, statistically significant differences in the expression of TXNIP, CXCL8, BAX, and CASP1 genes were confirmed by the RT-qPCR (p < 0.05). A STRING database analysis showed that the proteins encoded by the analyzed genes form a strong interaction network (p < 0.001). These data indicate that lutein modulates the expression level of pyroptosis-related genes, which may be useful for the development of new methods preventing pyroptosis pathway activation in the future. MDPI 2023-02-09 /pmc/articles/PMC9955508/ /pubmed/36826042 http://dx.doi.org/10.3390/cimb45020097 Text en © 2023 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
Strzalka-Mrozik, Barbara
Madej, Marcel
Kurowska, Natalia
Kruszniewska-Rajs, Celina
Kimsa-Dudek, Magdalena
Adamska, Jolanta
Gola, Joanna Magdalena
Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title_full Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title_fullStr Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title_full_unstemmed Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title_short Changes in the Expression Profile of Pyroptosis-Related Genes in Senescent Retinal Pigment Epithelial Cells after Lutein Treatment
title_sort changes in the expression profile of pyroptosis-related genes in senescent retinal pigment epithelial cells after lutein treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955508/
https://www.ncbi.nlm.nih.gov/pubmed/36826042
http://dx.doi.org/10.3390/cimb45020097
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