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Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia
Mammalian Müller glia express transcription factors and cell cycle regulators essential for the function of retinal progenitors, indicating the latent neurogenic capacity; however, the role of these regulators remains unclear. To gain insights into the role of these regulators in Müller glia, we ana...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666513/ https://www.ncbi.nlm.nih.gov/pubmed/36379991 http://dx.doi.org/10.1038/s41598-022-23855-w |
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author | Kato, Maki Sudou, Norihiro Nomura-Komoike, Kaori Iida, Tomohiro Fujieda, Hiroki |
author_facet | Kato, Maki Sudou, Norihiro Nomura-Komoike, Kaori Iida, Tomohiro Fujieda, Hiroki |
author_sort | Kato, Maki |
collection | PubMed |
description | Mammalian Müller glia express transcription factors and cell cycle regulators essential for the function of retinal progenitors, indicating the latent neurogenic capacity; however, the role of these regulators remains unclear. To gain insights into the role of these regulators in Müller glia, we analyzed expression of transcription factors (Pax6, Vsx2 and Nfia) and cell cycle regulators (cyclin D1 and D3) in rodent Müller glia, focusing on their age- and cell cycle-related expression patterns. Expression of Pax6, Vsx2, Nfia and cyclin D3, but not cyclin D1, increased in Müller glia during development. Photoreceptor injury induced cell cycle-associated increase of Vsx2 and cyclin D1, but not Pax6, Nfia, and cyclin D3. In dissociated cultures, cell cycle-associated increase of Pax6 and Vsx2 was observed in Müller glia from P10 mice but not from P21 mice. Nfia levels were highly correlated with EdU incorporation suggesting their activation during S phase progression. Cyclin D1 and D3 were transiently upregulated in G1 phase but downregulated after S phase entry. Our findings revealed previously unknown links between cell cycle progression and regulator protein expression, which likely affect the cell fate decision of proliferating Müller glia. |
format | Online Article Text |
id | pubmed-9666513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96665132022-11-17 Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia Kato, Maki Sudou, Norihiro Nomura-Komoike, Kaori Iida, Tomohiro Fujieda, Hiroki Sci Rep Article Mammalian Müller glia express transcription factors and cell cycle regulators essential for the function of retinal progenitors, indicating the latent neurogenic capacity; however, the role of these regulators remains unclear. To gain insights into the role of these regulators in Müller glia, we analyzed expression of transcription factors (Pax6, Vsx2 and Nfia) and cell cycle regulators (cyclin D1 and D3) in rodent Müller glia, focusing on their age- and cell cycle-related expression patterns. Expression of Pax6, Vsx2, Nfia and cyclin D3, but not cyclin D1, increased in Müller glia during development. Photoreceptor injury induced cell cycle-associated increase of Vsx2 and cyclin D1, but not Pax6, Nfia, and cyclin D3. In dissociated cultures, cell cycle-associated increase of Pax6 and Vsx2 was observed in Müller glia from P10 mice but not from P21 mice. Nfia levels were highly correlated with EdU incorporation suggesting their activation during S phase progression. Cyclin D1 and D3 were transiently upregulated in G1 phase but downregulated after S phase entry. Our findings revealed previously unknown links between cell cycle progression and regulator protein expression, which likely affect the cell fate decision of proliferating Müller glia. Nature Publishing Group UK 2022-11-15 /pmc/articles/PMC9666513/ /pubmed/36379991 http://dx.doi.org/10.1038/s41598-022-23855-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Kato, Maki Sudou, Norihiro Nomura-Komoike, Kaori Iida, Tomohiro Fujieda, Hiroki Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title | Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title_full | Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title_fullStr | Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title_full_unstemmed | Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title_short | Age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in Müller glia |
title_sort | age- and cell cycle-related expression patterns of transcription factors and cell cycle regulators in müller glia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666513/ https://www.ncbi.nlm.nih.gov/pubmed/36379991 http://dx.doi.org/10.1038/s41598-022-23855-w |
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