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Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney
The mammalian kidney develops through reciprocal interactions between the ureteric bud and the metanephric mesenchyme to give rise to the entire collecting system and the nephrons. Most of our knowledge of the developmental regulators driving this process arises from the study of gene expression and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124540/ https://www.ncbi.nlm.nih.gov/pubmed/30166318 http://dx.doi.org/10.1242/dev.164038 |
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author | Menon, Rajasree Otto, Edgar A. Kokoruda, Austin Zhou, Jian Zhang, Zidong Yoon, Euisik Chen, Yu-Chih Troyanskaya, Olga Spence, Jason R. Kretzler, Matthias Cebrián, Cristina |
author_facet | Menon, Rajasree Otto, Edgar A. Kokoruda, Austin Zhou, Jian Zhang, Zidong Yoon, Euisik Chen, Yu-Chih Troyanskaya, Olga Spence, Jason R. Kretzler, Matthias Cebrián, Cristina |
author_sort | Menon, Rajasree |
collection | PubMed |
description | The mammalian kidney develops through reciprocal interactions between the ureteric bud and the metanephric mesenchyme to give rise to the entire collecting system and the nephrons. Most of our knowledge of the developmental regulators driving this process arises from the study of gene expression and functional genetics in mice and other animal models. In order to shed light on human kidney development, we have used single-cell transcriptomics to characterize gene expression in different cell populations, and to study individual cell dynamics and lineage trajectories during development. Single-cell transcriptome analyses of 6414 cells from five individual specimens identified 11 initial clusters of specific renal cell types as defined by their gene expression profile. Further subclustering identifies progenitors, and mature and intermediate stages of differentiation for several renal lineages. Other lineages identified include mesangium, stroma, endothelial and immune cells. Novel markers for these cell types were revealed in the analysis, as were components of key signaling pathways driving renal development in animal models. Altogether, we provide a comprehensive and dynamic gene expression profile of the developing human kidney at the single-cell level. |
format | Online Article Text |
id | pubmed-6124540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61245402018-09-18 Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney Menon, Rajasree Otto, Edgar A. Kokoruda, Austin Zhou, Jian Zhang, Zidong Yoon, Euisik Chen, Yu-Chih Troyanskaya, Olga Spence, Jason R. Kretzler, Matthias Cebrián, Cristina Development Human Development The mammalian kidney develops through reciprocal interactions between the ureteric bud and the metanephric mesenchyme to give rise to the entire collecting system and the nephrons. Most of our knowledge of the developmental regulators driving this process arises from the study of gene expression and functional genetics in mice and other animal models. In order to shed light on human kidney development, we have used single-cell transcriptomics to characterize gene expression in different cell populations, and to study individual cell dynamics and lineage trajectories during development. Single-cell transcriptome analyses of 6414 cells from five individual specimens identified 11 initial clusters of specific renal cell types as defined by their gene expression profile. Further subclustering identifies progenitors, and mature and intermediate stages of differentiation for several renal lineages. Other lineages identified include mesangium, stroma, endothelial and immune cells. Novel markers for these cell types were revealed in the analysis, as were components of key signaling pathways driving renal development in animal models. Altogether, we provide a comprehensive and dynamic gene expression profile of the developing human kidney at the single-cell level. The Company of Biologists Ltd 2018-08-15 2018-08-30 /pmc/articles/PMC6124540/ /pubmed/30166318 http://dx.doi.org/10.1242/dev.164038 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Human Development Menon, Rajasree Otto, Edgar A. Kokoruda, Austin Zhou, Jian Zhang, Zidong Yoon, Euisik Chen, Yu-Chih Troyanskaya, Olga Spence, Jason R. Kretzler, Matthias Cebrián, Cristina Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title | Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title_full | Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title_fullStr | Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title_full_unstemmed | Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title_short | Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
title_sort | single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney |
topic | Human Development |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124540/ https://www.ncbi.nlm.nih.gov/pubmed/30166318 http://dx.doi.org/10.1242/dev.164038 |
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