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Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs
Single-cell RNA sequencing has recently led to the identification of a flurry of rare, new cell types, such as the CFTR-high ionocytes in the airway epithelium. Ionocytes appear to be specifically responsible for fluid osmolarity and pH regulation. Similar cells exist in multiple other organs and ha...
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/PMC9981729/ https://www.ncbi.nlm.nih.gov/pubmed/36864051 http://dx.doi.org/10.1038/s41598-023-30603-1 |
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author | Pou Casellas, Carla Pleguezuelos-Manzano, Cayetano Rookmaaker, Maarten B. Verhaar, Marianne C. Clevers, Hans |
author_facet | Pou Casellas, Carla Pleguezuelos-Manzano, Cayetano Rookmaaker, Maarten B. Verhaar, Marianne C. Clevers, Hans |
author_sort | Pou Casellas, Carla |
collection | PubMed |
description | Single-cell RNA sequencing has recently led to the identification of a flurry of rare, new cell types, such as the CFTR-high ionocytes in the airway epithelium. Ionocytes appear to be specifically responsible for fluid osmolarity and pH regulation. Similar cells exist in multiple other organs and have received various names, including intercalated cell in the kidney, mitochondria-rich cell in the inner ear, clear cell in the epididymis, and ionocyte in the salivary gland. Here, we compare the previously published transcriptomic profile of cells expressing FOXI1, the signature transcription factor expressed in airway ionocytes. Such FOXI1+ cells were found in datasets representing human and/or murine kidney, airway, epididymis, thymus, skin, inner ear, salivary gland, and prostate. This allowed us to assess the similarities between these cells and identify the core transcriptomic signature of this ionocyte ‘family’. Our results demonstrate that, across all these organs, ionocytes maintain the expression of a characteristic set of genes, including FOXI1, KRT7, and ATP6V1B1. We conclude that the ionocyte signature defines a class of closely related cell types across multiple mammalian organs. |
format | Online Article Text |
id | pubmed-9981729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99817292023-03-04 Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs Pou Casellas, Carla Pleguezuelos-Manzano, Cayetano Rookmaaker, Maarten B. Verhaar, Marianne C. Clevers, Hans Sci Rep Article Single-cell RNA sequencing has recently led to the identification of a flurry of rare, new cell types, such as the CFTR-high ionocytes in the airway epithelium. Ionocytes appear to be specifically responsible for fluid osmolarity and pH regulation. Similar cells exist in multiple other organs and have received various names, including intercalated cell in the kidney, mitochondria-rich cell in the inner ear, clear cell in the epididymis, and ionocyte in the salivary gland. Here, we compare the previously published transcriptomic profile of cells expressing FOXI1, the signature transcription factor expressed in airway ionocytes. Such FOXI1+ cells were found in datasets representing human and/or murine kidney, airway, epididymis, thymus, skin, inner ear, salivary gland, and prostate. This allowed us to assess the similarities between these cells and identify the core transcriptomic signature of this ionocyte ‘family’. Our results demonstrate that, across all these organs, ionocytes maintain the expression of a characteristic set of genes, including FOXI1, KRT7, and ATP6V1B1. We conclude that the ionocyte signature defines a class of closely related cell types across multiple mammalian organs. Nature Publishing Group UK 2023-03-02 /pmc/articles/PMC9981729/ /pubmed/36864051 http://dx.doi.org/10.1038/s41598-023-30603-1 Text en © The Author(s) 2023, corrected publication 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 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 Pou Casellas, Carla Pleguezuelos-Manzano, Cayetano Rookmaaker, Maarten B. Verhaar, Marianne C. Clevers, Hans Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title | Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title_full | Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title_fullStr | Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title_full_unstemmed | Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title_short | Transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
title_sort | transcriptomic profile comparison reveals conservation of ionocytes across multiple organs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981729/ https://www.ncbi.nlm.nih.gov/pubmed/36864051 http://dx.doi.org/10.1038/s41598-023-30603-1 |
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