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Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics
The utricle is a vestibular sensory organ that requires mechanosensitive hair cells to detect linear acceleration. In neonatal mice, new hair cells are derived from non-sensory supporting cells, yet cell type diversity and mechanisms of cell addition remain poorly characterized. Here, we perform com...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378666/ https://www.ncbi.nlm.nih.gov/pubmed/34260939 http://dx.doi.org/10.1016/j.celrep.2021.109358 |
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author | Jan, Taha A. Eltawil, Yasmin Ling, Angela H. Chen, Leon Ellwanger, Daniel C. Heller, Stefan Cheng, Alan G. |
author_facet | Jan, Taha A. Eltawil, Yasmin Ling, Angela H. Chen, Leon Ellwanger, Daniel C. Heller, Stefan Cheng, Alan G. |
author_sort | Jan, Taha A. |
collection | PubMed |
description | The utricle is a vestibular sensory organ that requires mechanosensitive hair cells to detect linear acceleration. In neonatal mice, new hair cells are derived from non-sensory supporting cells, yet cell type diversity and mechanisms of cell addition remain poorly characterized. Here, we perform computational analyses on single-cell transcriptomes to categorize cell types and resolve 14 individual sensory and non-sensory subtypes. Along the periphery of the sensory epithelium, we uncover distinct groups of transitional epithelial cells, marked by Islr, Cnmd, and Enpep expression. By reconstructing de novo trajectories and gene dynamics, we show that as the utricle expands, Islr(+) transitional epithelial cells exhibit a dynamic and proliferative phase to generate new supporting cells, followed by coordinated differentiation into hair cells. Taken together, our study reveals a sequential and coordinated process by which non-sensory epithelial cells contribute to growth of the postnatal mouse sensory epithelium. |
format | Online Article Text |
id | pubmed-8378666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-83786662021-08-20 Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics Jan, Taha A. Eltawil, Yasmin Ling, Angela H. Chen, Leon Ellwanger, Daniel C. Heller, Stefan Cheng, Alan G. Cell Rep Article The utricle is a vestibular sensory organ that requires mechanosensitive hair cells to detect linear acceleration. In neonatal mice, new hair cells are derived from non-sensory supporting cells, yet cell type diversity and mechanisms of cell addition remain poorly characterized. Here, we perform computational analyses on single-cell transcriptomes to categorize cell types and resolve 14 individual sensory and non-sensory subtypes. Along the periphery of the sensory epithelium, we uncover distinct groups of transitional epithelial cells, marked by Islr, Cnmd, and Enpep expression. By reconstructing de novo trajectories and gene dynamics, we show that as the utricle expands, Islr(+) transitional epithelial cells exhibit a dynamic and proliferative phase to generate new supporting cells, followed by coordinated differentiation into hair cells. Taken together, our study reveals a sequential and coordinated process by which non-sensory epithelial cells contribute to growth of the postnatal mouse sensory epithelium. 2021-07-13 /pmc/articles/PMC8378666/ /pubmed/34260939 http://dx.doi.org/10.1016/j.celrep.2021.109358 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Jan, Taha A. Eltawil, Yasmin Ling, Angela H. Chen, Leon Ellwanger, Daniel C. Heller, Stefan Cheng, Alan G. Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title | Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title_full | Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title_fullStr | Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title_full_unstemmed | Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title_short | Spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
title_sort | spatiotemporal dynamics of inner ear sensory and non-sensory cells revealed by single-cell transcriptomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378666/ https://www.ncbi.nlm.nih.gov/pubmed/34260939 http://dx.doi.org/10.1016/j.celrep.2021.109358 |
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