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Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis

BACKGROUND: Organogenesis is crucial for proper organ formation during mammalian embryonic development. However, the similarities and shared features between different organs and the cellular heterogeneity during this process at single-cell resolution remain elusive. RESULTS: We perform single-cell...

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Autores principales: Dong, Ji, Hu, Yuqiong, Fan, Xiaoying, Wu, Xinglong, Mao, Yunuo, Hu, Boqiang, Guo, Hongshan, Wen, Lu, Tang, Fuchou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853091/
https://www.ncbi.nlm.nih.gov/pubmed/29540203
http://dx.doi.org/10.1186/s13059-018-1416-2
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author Dong, Ji
Hu, Yuqiong
Fan, Xiaoying
Wu, Xinglong
Mao, Yunuo
Hu, Boqiang
Guo, Hongshan
Wen, Lu
Tang, Fuchou
author_facet Dong, Ji
Hu, Yuqiong
Fan, Xiaoying
Wu, Xinglong
Mao, Yunuo
Hu, Boqiang
Guo, Hongshan
Wen, Lu
Tang, Fuchou
author_sort Dong, Ji
collection PubMed
description BACKGROUND: Organogenesis is crucial for proper organ formation during mammalian embryonic development. However, the similarities and shared features between different organs and the cellular heterogeneity during this process at single-cell resolution remain elusive. RESULTS: We perform single-cell RNA sequencing analysis of 1916 individual cells from eight organs and tissues of E9.5 to E11.5 mouse embryos, namely, the forebrain, hindbrain, skin, heart, somite, lung, liver, and intestine. Based on the regulatory activities rather than the expression patterns, all cells analyzed can be well classified into four major groups with epithelial, mesodermal, hematopoietic, and neuronal identities. For different organs within the same group, the similarities and differences of their features and developmental paths are revealed and reconstructed. CONCLUSIONS: We identify mutual interactions between epithelial and mesenchymal cells and detect epithelial cells with prevalent mesenchymal features during organogenesis, which are similar to the features of intermediate epithelial/mesenchymal cells during tumorigenesis. The comprehensive transcriptome at single-cell resolution profiled in our study paves the way for future mechanistic studies of the gene-regulatory networks governing mammalian organogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1416-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-58530912018-03-22 Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis Dong, Ji Hu, Yuqiong Fan, Xiaoying Wu, Xinglong Mao, Yunuo Hu, Boqiang Guo, Hongshan Wen, Lu Tang, Fuchou Genome Biol Research Article BACKGROUND: Organogenesis is crucial for proper organ formation during mammalian embryonic development. However, the similarities and shared features between different organs and the cellular heterogeneity during this process at single-cell resolution remain elusive. RESULTS: We perform single-cell RNA sequencing analysis of 1916 individual cells from eight organs and tissues of E9.5 to E11.5 mouse embryos, namely, the forebrain, hindbrain, skin, heart, somite, lung, liver, and intestine. Based on the regulatory activities rather than the expression patterns, all cells analyzed can be well classified into four major groups with epithelial, mesodermal, hematopoietic, and neuronal identities. For different organs within the same group, the similarities and differences of their features and developmental paths are revealed and reconstructed. CONCLUSIONS: We identify mutual interactions between epithelial and mesenchymal cells and detect epithelial cells with prevalent mesenchymal features during organogenesis, which are similar to the features of intermediate epithelial/mesenchymal cells during tumorigenesis. The comprehensive transcriptome at single-cell resolution profiled in our study paves the way for future mechanistic studies of the gene-regulatory networks governing mammalian organogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1416-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-14 /pmc/articles/PMC5853091/ /pubmed/29540203 http://dx.doi.org/10.1186/s13059-018-1416-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Dong, Ji
Hu, Yuqiong
Fan, Xiaoying
Wu, Xinglong
Mao, Yunuo
Hu, Boqiang
Guo, Hongshan
Wen, Lu
Tang, Fuchou
Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title_full Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title_fullStr Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title_full_unstemmed Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title_short Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
title_sort single-cell rna-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853091/
https://www.ncbi.nlm.nih.gov/pubmed/29540203
http://dx.doi.org/10.1186/s13059-018-1416-2
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