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Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish

The current view of hematopoiesis considers leukocytes on a continuum with distinct developmental origins, and which exert non-overlapping functions. However, there is less known about the function and phenotype of ontogenetically distinct neutrophil populations. In this work, using a photoconvertib...

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Autores principales: García-López, Juan P., Grimaldi, Alexandre, Chen, Zelin, Meneses, Claudio, Bravo-Tello, Karina, Bresciani, Erica, Banderas, Alvaro, Burgess, Shawn M., Hernández, Pedro P., Feijoo, Carmen G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427629/
https://www.ncbi.nlm.nih.gov/pubmed/37582932
http://dx.doi.org/10.1038/s41467-023-40662-7
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author García-López, Juan P.
Grimaldi, Alexandre
Chen, Zelin
Meneses, Claudio
Bravo-Tello, Karina
Bresciani, Erica
Banderas, Alvaro
Burgess, Shawn M.
Hernández, Pedro P.
Feijoo, Carmen G.
author_facet García-López, Juan P.
Grimaldi, Alexandre
Chen, Zelin
Meneses, Claudio
Bravo-Tello, Karina
Bresciani, Erica
Banderas, Alvaro
Burgess, Shawn M.
Hernández, Pedro P.
Feijoo, Carmen G.
author_sort García-López, Juan P.
collection PubMed
description The current view of hematopoiesis considers leukocytes on a continuum with distinct developmental origins, and which exert non-overlapping functions. However, there is less known about the function and phenotype of ontogenetically distinct neutrophil populations. In this work, using a photoconvertible transgenic zebrafish line; Tg(mpx:Dendra2), we selectively label rostral blood island-derived and caudal hematopoietic tissue-derived neutrophils in vivo during steady state or upon injury. By comparing the migratory properties and single-cell expression profiles of both neutrophil populations at steady state we show that rostral neutrophils show higher csf3b expression and migration capacity than caudal neutrophils. Upon injury, both populations share a core transcriptional profile as well as subset-specific transcriptional signatures. Accordingly, both rostral and caudal neutrophils are recruited to the wound independently of their distance to the injury. While rostral neutrophils respond uniformly, caudal neutrophils respond heterogeneously. Collectively, our results reveal that co-existing neutrophils populations with ontogenically distinct origin display functional differences.
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spelling pubmed-104276292023-08-17 Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish García-López, Juan P. Grimaldi, Alexandre Chen, Zelin Meneses, Claudio Bravo-Tello, Karina Bresciani, Erica Banderas, Alvaro Burgess, Shawn M. Hernández, Pedro P. Feijoo, Carmen G. Nat Commun Article The current view of hematopoiesis considers leukocytes on a continuum with distinct developmental origins, and which exert non-overlapping functions. However, there is less known about the function and phenotype of ontogenetically distinct neutrophil populations. In this work, using a photoconvertible transgenic zebrafish line; Tg(mpx:Dendra2), we selectively label rostral blood island-derived and caudal hematopoietic tissue-derived neutrophils in vivo during steady state or upon injury. By comparing the migratory properties and single-cell expression profiles of both neutrophil populations at steady state we show that rostral neutrophils show higher csf3b expression and migration capacity than caudal neutrophils. Upon injury, both populations share a core transcriptional profile as well as subset-specific transcriptional signatures. Accordingly, both rostral and caudal neutrophils are recruited to the wound independently of their distance to the injury. While rostral neutrophils respond uniformly, caudal neutrophils respond heterogeneously. Collectively, our results reveal that co-existing neutrophils populations with ontogenically distinct origin display functional differences. Nature Publishing Group UK 2023-08-15 /pmc/articles/PMC10427629/ /pubmed/37582932 http://dx.doi.org/10.1038/s41467-023-40662-7 Text en © The Author(s) 2023, corrected publication 2023 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
García-López, Juan P.
Grimaldi, Alexandre
Chen, Zelin
Meneses, Claudio
Bravo-Tello, Karina
Bresciani, Erica
Banderas, Alvaro
Burgess, Shawn M.
Hernández, Pedro P.
Feijoo, Carmen G.
Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title_full Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title_fullStr Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title_full_unstemmed Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title_short Ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
title_sort ontogenetically distinct neutrophils differ in function and transcriptional profile in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427629/
https://www.ncbi.nlm.nih.gov/pubmed/37582932
http://dx.doi.org/10.1038/s41467-023-40662-7
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