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Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction
The function and heterogeneity of neutrophils in neonatal umbilical cord blood (UCB) have not been characterized. In this study, we analyzed the neutrophils in UCB and healthy adults using single-cell RNA sequencing analysis for the first time. We found that neutrophils divided into six subpopulatio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464600/ https://www.ncbi.nlm.nih.gov/pubmed/36105817 http://dx.doi.org/10.3389/fimmu.2022.970909 |
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author | Chen, Yi Huang, Jiamin Guo, Zaiwen Zhu, Zhechen Shao, Yiming Li, Linbin Yang, Yunxi Yu, Yanzhen Liu, Lu Sun, Bingwei |
author_facet | Chen, Yi Huang, Jiamin Guo, Zaiwen Zhu, Zhechen Shao, Yiming Li, Linbin Yang, Yunxi Yu, Yanzhen Liu, Lu Sun, Bingwei |
author_sort | Chen, Yi |
collection | PubMed |
description | The function and heterogeneity of neutrophils in neonatal umbilical cord blood (UCB) have not been characterized. In this study, we analyzed the neutrophils in UCB and healthy adults using single-cell RNA sequencing analysis for the first time. We found that neutrophils divided into six subpopulations (G2, G3, G4, G5a, G5b, and G5c) with different marker genes and different functions under homeostasis. Compared with healthy adults, neutrophils of UCB were more naïve and have more obvious degranulation and activation functions. Moreover, we found significant differences in the amount and function of G5b cells between healthy adults and UCB. The amount of G5b group in UCB was lower, but it has more degranulation, secretion and activation functions. In addition, we noted a new subset of G5c labeled by CD52, which almost did not exist in UCB. Besides, its differential genes were enriched in terms such as protein synthesis and mRNA transcription. Furthermore, uncharacteristic transcription factors ZNF-276, ZNF-319 and ZNF-354A were identified in our study. In summary, we first examined the heterogeneity and functional diversity of neutrophils in UCB, and these data provided new insights into the mechanism of neutrophil-mediated diseases of neonates and the wider use of neutrophils in UCB. |
format | Online Article Text |
id | pubmed-9464600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94646002022-09-13 Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction Chen, Yi Huang, Jiamin Guo, Zaiwen Zhu, Zhechen Shao, Yiming Li, Linbin Yang, Yunxi Yu, Yanzhen Liu, Lu Sun, Bingwei Front Immunol Immunology The function and heterogeneity of neutrophils in neonatal umbilical cord blood (UCB) have not been characterized. In this study, we analyzed the neutrophils in UCB and healthy adults using single-cell RNA sequencing analysis for the first time. We found that neutrophils divided into six subpopulations (G2, G3, G4, G5a, G5b, and G5c) with different marker genes and different functions under homeostasis. Compared with healthy adults, neutrophils of UCB were more naïve and have more obvious degranulation and activation functions. Moreover, we found significant differences in the amount and function of G5b cells between healthy adults and UCB. The amount of G5b group in UCB was lower, but it has more degranulation, secretion and activation functions. In addition, we noted a new subset of G5c labeled by CD52, which almost did not exist in UCB. Besides, its differential genes were enriched in terms such as protein synthesis and mRNA transcription. Furthermore, uncharacteristic transcription factors ZNF-276, ZNF-319 and ZNF-354A were identified in our study. In summary, we first examined the heterogeneity and functional diversity of neutrophils in UCB, and these data provided new insights into the mechanism of neutrophil-mediated diseases of neonates and the wider use of neutrophils in UCB. Frontiers Media S.A. 2022-08-29 /pmc/articles/PMC9464600/ /pubmed/36105817 http://dx.doi.org/10.3389/fimmu.2022.970909 Text en Copyright © 2022 Chen, Huang, Guo, Zhu, Shao, Li, Yang, Yu, Liu and Sun https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chen, Yi Huang, Jiamin Guo, Zaiwen Zhu, Zhechen Shao, Yiming Li, Linbin Yang, Yunxi Yu, Yanzhen Liu, Lu Sun, Bingwei Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title | Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title_full | Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title_fullStr | Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title_full_unstemmed | Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title_short | Primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
title_sort | primitive genotypic characteristics in umbilical cord neutrophils identified by single-cell transcriptome profiling and functional prediction |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464600/ https://www.ncbi.nlm.nih.gov/pubmed/36105817 http://dx.doi.org/10.3389/fimmu.2022.970909 |
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