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Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos
Vascular endothelial cells exhibit substantial phenotypic and transcriptional heterogeneity which is established during early embryogenesis. However, the molecular mechanisms involved in establishing endothelial cell diversity are still not well understood. Zebrafish has emerged as an advantageous m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338088/ https://www.ncbi.nlm.nih.gov/pubmed/35906287 http://dx.doi.org/10.1038/s41598-022-17127-w |
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author | Gurung, Suman Restrepo, Nicole K. Chestnut, Brendan Klimkaite, Laurita Sumanas, Saulius |
author_facet | Gurung, Suman Restrepo, Nicole K. Chestnut, Brendan Klimkaite, Laurita Sumanas, Saulius |
author_sort | Gurung, Suman |
collection | PubMed |
description | Vascular endothelial cells exhibit substantial phenotypic and transcriptional heterogeneity which is established during early embryogenesis. However, the molecular mechanisms involved in establishing endothelial cell diversity are still not well understood. Zebrafish has emerged as an advantageous model to study vascular development. Despite its importance, the single-cell transcriptomic profile of vascular endothelial cells during zebrafish development is still missing. To address this, we applied single-cell RNA-sequencing (scRNA-seq) of vascular endothelial cells isolated from zebrafish embryos at the 24 hpf stage. Six distinct clusters or subclusters related to vascular endothelial cells were identified which include arterial, two venous, cranial, endocardial and endothelial progenitor cell subtypes. Furthermore, we validated our findings by characterizing novel markers for arterial, venous, and endocardial cells. We experimentally confirmed the presence of two transcriptionally different venous cell subtypes, demonstrating heterogeneity among venous endothelial cells at this early developmental stage. This dataset will be a valuable resource for future functional characterization of vascular endothelial cells and interrogation of molecular mechanisms involved in the establishment of their heterogeneity and cell-fate decisions. |
format | Online Article Text |
id | pubmed-9338088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93380882022-07-31 Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos Gurung, Suman Restrepo, Nicole K. Chestnut, Brendan Klimkaite, Laurita Sumanas, Saulius Sci Rep Article Vascular endothelial cells exhibit substantial phenotypic and transcriptional heterogeneity which is established during early embryogenesis. However, the molecular mechanisms involved in establishing endothelial cell diversity are still not well understood. Zebrafish has emerged as an advantageous model to study vascular development. Despite its importance, the single-cell transcriptomic profile of vascular endothelial cells during zebrafish development is still missing. To address this, we applied single-cell RNA-sequencing (scRNA-seq) of vascular endothelial cells isolated from zebrafish embryos at the 24 hpf stage. Six distinct clusters or subclusters related to vascular endothelial cells were identified which include arterial, two venous, cranial, endocardial and endothelial progenitor cell subtypes. Furthermore, we validated our findings by characterizing novel markers for arterial, venous, and endocardial cells. We experimentally confirmed the presence of two transcriptionally different venous cell subtypes, demonstrating heterogeneity among venous endothelial cells at this early developmental stage. This dataset will be a valuable resource for future functional characterization of vascular endothelial cells and interrogation of molecular mechanisms involved in the establishment of their heterogeneity and cell-fate decisions. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9338088/ /pubmed/35906287 http://dx.doi.org/10.1038/s41598-022-17127-w Text en © The Author(s) 2022 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 Gurung, Suman Restrepo, Nicole K. Chestnut, Brendan Klimkaite, Laurita Sumanas, Saulius Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title | Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title_full | Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title_fullStr | Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title_full_unstemmed | Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title_short | Single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
title_sort | single-cell transcriptomic analysis of vascular endothelial cells in zebrafish embryos |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338088/ https://www.ncbi.nlm.nih.gov/pubmed/35906287 http://dx.doi.org/10.1038/s41598-022-17127-w |
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