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Whole transcriptome profiling of taste bud cells
Analysis of single-cell RNA-Seq data can provide insights into the specific functions of individual cell types that compose complex tissues. Here, we examined gene expression in two distinct subpopulations of mouse taste cells: Tas1r3-expressing type II cells and physiologically identified type III...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548921/ https://www.ncbi.nlm.nih.gov/pubmed/28790351 http://dx.doi.org/10.1038/s41598-017-07746-z |
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author | Sukumaran, Sunil K. Lewandowski, Brian C. Qin, Yumei Kotha, Ramana Bachmanov, Alexander A. Margolskee, Robert F. |
author_facet | Sukumaran, Sunil K. Lewandowski, Brian C. Qin, Yumei Kotha, Ramana Bachmanov, Alexander A. Margolskee, Robert F. |
author_sort | Sukumaran, Sunil K. |
collection | PubMed |
description | Analysis of single-cell RNA-Seq data can provide insights into the specific functions of individual cell types that compose complex tissues. Here, we examined gene expression in two distinct subpopulations of mouse taste cells: Tas1r3-expressing type II cells and physiologically identified type III cells. Our RNA-Seq libraries met high quality control standards and accurately captured differential expression of marker genes for type II (e.g. the Tas1r genes, Plcb2, Trpm5) and type III (e.g. Pkd2l1, Ncam, Snap25) taste cells. Bioinformatics analysis showed that genes regulating responses to stimuli were up-regulated in type II cells, while pathways related to neuronal function were up-regulated in type III cells. We also identified highly expressed genes and pathways associated with chemotaxis and axon guidance, providing new insights into the mechanisms underlying integration of new taste cells into the taste bud. We validated our results by immunohistochemically confirming expression of selected genes encoding synaptic (Cplx2 and Pclo) and semaphorin signalling pathway (Crmp2, PlexinB1, Fes and Sema4a) components. The approach described here could provide a comprehensive map of gene expression for all taste cell subpopulations and will be particularly relevant for cell types in taste buds and other tissues that can be identified only by physiological methods. |
format | Online Article Text |
id | pubmed-5548921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55489212017-08-09 Whole transcriptome profiling of taste bud cells Sukumaran, Sunil K. Lewandowski, Brian C. Qin, Yumei Kotha, Ramana Bachmanov, Alexander A. Margolskee, Robert F. Sci Rep Article Analysis of single-cell RNA-Seq data can provide insights into the specific functions of individual cell types that compose complex tissues. Here, we examined gene expression in two distinct subpopulations of mouse taste cells: Tas1r3-expressing type II cells and physiologically identified type III cells. Our RNA-Seq libraries met high quality control standards and accurately captured differential expression of marker genes for type II (e.g. the Tas1r genes, Plcb2, Trpm5) and type III (e.g. Pkd2l1, Ncam, Snap25) taste cells. Bioinformatics analysis showed that genes regulating responses to stimuli were up-regulated in type II cells, while pathways related to neuronal function were up-regulated in type III cells. We also identified highly expressed genes and pathways associated with chemotaxis and axon guidance, providing new insights into the mechanisms underlying integration of new taste cells into the taste bud. We validated our results by immunohistochemically confirming expression of selected genes encoding synaptic (Cplx2 and Pclo) and semaphorin signalling pathway (Crmp2, PlexinB1, Fes and Sema4a) components. The approach described here could provide a comprehensive map of gene expression for all taste cell subpopulations and will be particularly relevant for cell types in taste buds and other tissues that can be identified only by physiological methods. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548921/ /pubmed/28790351 http://dx.doi.org/10.1038/s41598-017-07746-z Text en © The Author(s) 2017 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/. |
spellingShingle | Article Sukumaran, Sunil K. Lewandowski, Brian C. Qin, Yumei Kotha, Ramana Bachmanov, Alexander A. Margolskee, Robert F. Whole transcriptome profiling of taste bud cells |
title | Whole transcriptome profiling of taste bud cells |
title_full | Whole transcriptome profiling of taste bud cells |
title_fullStr | Whole transcriptome profiling of taste bud cells |
title_full_unstemmed | Whole transcriptome profiling of taste bud cells |
title_short | Whole transcriptome profiling of taste bud cells |
title_sort | whole transcriptome profiling of taste bud cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548921/ https://www.ncbi.nlm.nih.gov/pubmed/28790351 http://dx.doi.org/10.1038/s41598-017-07746-z |
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