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Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury
Taste receptor cells are taste bud epithelial cells that are dependent upon the innervating nerve for continuous renewal and are maintained by resident tissue stem/progenitor cells. Transection of the innervating nerve causes degeneration of taste buds and taste receptor cells. However, a subset of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833027/ https://www.ncbi.nlm.nih.gov/pubmed/36631663 http://dx.doi.org/10.1038/s12276-022-00924-8 |
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author | Adpaikar, Anish Ashok Lee, Jong-Min Lee, Dong-Joon Cho, Hye-Yeon Ohshima, Hayato Moon, Seok Jun Jung, Han-Sung |
author_facet | Adpaikar, Anish Ashok Lee, Jong-Min Lee, Dong-Joon Cho, Hye-Yeon Ohshima, Hayato Moon, Seok Jun Jung, Han-Sung |
author_sort | Adpaikar, Anish Ashok |
collection | PubMed |
description | Taste receptor cells are taste bud epithelial cells that are dependent upon the innervating nerve for continuous renewal and are maintained by resident tissue stem/progenitor cells. Transection of the innervating nerve causes degeneration of taste buds and taste receptor cells. However, a subset of the taste receptor cells is maintained without nerve contact after glossopharyngeal nerve transection in the circumvallate papilla in adult mice. Here, we revealed that injury caused by glossopharyngeal nerve transection triggers the remaining differentiated K8-positive taste receptor cells to dedifferentiate and acquire transient progenitor cell-like states during regeneration. Dedifferentiated taste receptor cells proliferate, express progenitor cell markers (K14, Sox2, PCNA) and form organoids in vitro. These data indicate that differentiated taste receptor cells can enter the cell cycle, acquire stemness, and participate in taste bud regeneration. We propose that dedifferentiated taste receptor cells in combination with stem/progenitor cells enhance the regeneration of taste buds following nerve injury. |
format | Online Article Text |
id | pubmed-9833027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98330272023-01-12 Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury Adpaikar, Anish Ashok Lee, Jong-Min Lee, Dong-Joon Cho, Hye-Yeon Ohshima, Hayato Moon, Seok Jun Jung, Han-Sung Exp Mol Med Article Taste receptor cells are taste bud epithelial cells that are dependent upon the innervating nerve for continuous renewal and are maintained by resident tissue stem/progenitor cells. Transection of the innervating nerve causes degeneration of taste buds and taste receptor cells. However, a subset of the taste receptor cells is maintained without nerve contact after glossopharyngeal nerve transection in the circumvallate papilla in adult mice. Here, we revealed that injury caused by glossopharyngeal nerve transection triggers the remaining differentiated K8-positive taste receptor cells to dedifferentiate and acquire transient progenitor cell-like states during regeneration. Dedifferentiated taste receptor cells proliferate, express progenitor cell markers (K14, Sox2, PCNA) and form organoids in vitro. These data indicate that differentiated taste receptor cells can enter the cell cycle, acquire stemness, and participate in taste bud regeneration. We propose that dedifferentiated taste receptor cells in combination with stem/progenitor cells enhance the regeneration of taste buds following nerve injury. Nature Publishing Group UK 2023-01-11 /pmc/articles/PMC9833027/ /pubmed/36631663 http://dx.doi.org/10.1038/s12276-022-00924-8 Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Adpaikar, Anish Ashok Lee, Jong-Min Lee, Dong-Joon Cho, Hye-Yeon Ohshima, Hayato Moon, Seok Jun Jung, Han-Sung Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title | Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title_full | Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title_fullStr | Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title_full_unstemmed | Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title_short | Epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
title_sort | epithelial plasticity enhances regeneration of committed taste receptor cells following nerve injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833027/ https://www.ncbi.nlm.nih.gov/pubmed/36631663 http://dx.doi.org/10.1038/s12276-022-00924-8 |
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