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When blood development meets single-cell transcriptomics

Blood cells arise during embryonic development by three temporally distinct waves. Belonging to the third wave, hematopoietic stem cells (HSCs) are generated from hemogenic endothelium via endothelial-to-hematopoietic transition in mid-gestational embryos. Recently, studies combined with single-cell...

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Detalles Bibliográficos
Autores principales: Zhou, Jie, Liu, Bing, Lan, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974905/
https://www.ncbi.nlm.nih.gov/pubmed/35402794
http://dx.doi.org/10.1097/BS9.0000000000000007
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author Zhou, Jie
Liu, Bing
Lan, Yu
author_facet Zhou, Jie
Liu, Bing
Lan, Yu
author_sort Zhou, Jie
collection PubMed
description Blood cells arise during embryonic development by three temporally distinct waves. Belonging to the third wave, hematopoietic stem cells (HSCs) are generated from hemogenic endothelium via endothelial-to-hematopoietic transition in mid-gestational embryos. Recently, studies combined with single-cell transcriptomics have provided massive new insights into the molecular evolutions and the underlying mechanisms of distinct waves of hematopoietic specification. In this review, we discuss the current single-cell profiling techniques, the most recent novel findings involved in the generation of distinct waves of blood cells, especially the HSCs, using single-cell transcriptional profiling combined with functional evaluations, and the perspectives to use the accumulating huge single-cell transcriptional data sets to study developmental hematopoiesis.
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spelling pubmed-89749052022-04-07 When blood development meets single-cell transcriptomics Zhou, Jie Liu, Bing Lan, Yu Blood Sci Mini-Reviews Blood cells arise during embryonic development by three temporally distinct waves. Belonging to the third wave, hematopoietic stem cells (HSCs) are generated from hemogenic endothelium via endothelial-to-hematopoietic transition in mid-gestational embryos. Recently, studies combined with single-cell transcriptomics have provided massive new insights into the molecular evolutions and the underlying mechanisms of distinct waves of hematopoietic specification. In this review, we discuss the current single-cell profiling techniques, the most recent novel findings involved in the generation of distinct waves of blood cells, especially the HSCs, using single-cell transcriptional profiling combined with functional evaluations, and the perspectives to use the accumulating huge single-cell transcriptional data sets to study developmental hematopoiesis. Wolters Kluwer Health 2019-09-17 /pmc/articles/PMC8974905/ /pubmed/35402794 http://dx.doi.org/10.1097/BS9.0000000000000007 Text en Copyright © 2019 The Authors. Published by Wolters Kluwer Health Inc., on behalf of the Chinese Association for Blood Sciences. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Mini-Reviews
Zhou, Jie
Liu, Bing
Lan, Yu
When blood development meets single-cell transcriptomics
title When blood development meets single-cell transcriptomics
title_full When blood development meets single-cell transcriptomics
title_fullStr When blood development meets single-cell transcriptomics
title_full_unstemmed When blood development meets single-cell transcriptomics
title_short When blood development meets single-cell transcriptomics
title_sort when blood development meets single-cell transcriptomics
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974905/
https://www.ncbi.nlm.nih.gov/pubmed/35402794
http://dx.doi.org/10.1097/BS9.0000000000000007
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