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Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1

Haematopoietic stem cells (HSCs) are characterized by their self-renewal potential associated to dormancy. Here we identify the cell surface receptor neogenin-1 as specifically expressed in dormant HSCs. Loss of neogenin-1 initially leads to increased HSC expansion but subsequently to loss of self-r...

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Autores principales: Renders, Simon, Svendsen, Arthur Flohr, Panten, Jasper, Rama, Nicolas, Maryanovich, Maria, Sommerkamp, Pia, Ladel, Luisa, Redavid, Anna Rita, Gibert, Benjamin, Lazare, Seka, Ducarouge, Benjamin, Schönberger, Katharina, Narr, Andreas, Tourbez, Manon, Dethmers-Ausema, Bertien, Zwart, Erik, Hotz-Wagenblatt, Agnes, Zhang, Dachuan, Korn, Claudia, Zeisberger, Petra, Przybylla, Adriana, Sohn, Markus, Mendez-Ferrer, Simon, Heikenwälder, Mathias, Brune, Maik, Klimmeck, Daniel, Bystrykh, Leonid, Frenette, Paul S., Mehlen, Patrick, de Haan, Gerald, Cabezas-Wallscheid, Nina, Trumpp, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840807/
https://www.ncbi.nlm.nih.gov/pubmed/33504783
http://dx.doi.org/10.1038/s41467-020-20801-0
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author Renders, Simon
Svendsen, Arthur Flohr
Panten, Jasper
Rama, Nicolas
Maryanovich, Maria
Sommerkamp, Pia
Ladel, Luisa
Redavid, Anna Rita
Gibert, Benjamin
Lazare, Seka
Ducarouge, Benjamin
Schönberger, Katharina
Narr, Andreas
Tourbez, Manon
Dethmers-Ausema, Bertien
Zwart, Erik
Hotz-Wagenblatt, Agnes
Zhang, Dachuan
Korn, Claudia
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Mendez-Ferrer, Simon
Heikenwälder, Mathias
Brune, Maik
Klimmeck, Daniel
Bystrykh, Leonid
Frenette, Paul S.
Mehlen, Patrick
de Haan, Gerald
Cabezas-Wallscheid, Nina
Trumpp, Andreas
author_facet Renders, Simon
Svendsen, Arthur Flohr
Panten, Jasper
Rama, Nicolas
Maryanovich, Maria
Sommerkamp, Pia
Ladel, Luisa
Redavid, Anna Rita
Gibert, Benjamin
Lazare, Seka
Ducarouge, Benjamin
Schönberger, Katharina
Narr, Andreas
Tourbez, Manon
Dethmers-Ausema, Bertien
Zwart, Erik
Hotz-Wagenblatt, Agnes
Zhang, Dachuan
Korn, Claudia
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Mendez-Ferrer, Simon
Heikenwälder, Mathias
Brune, Maik
Klimmeck, Daniel
Bystrykh, Leonid
Frenette, Paul S.
Mehlen, Patrick
de Haan, Gerald
Cabezas-Wallscheid, Nina
Trumpp, Andreas
author_sort Renders, Simon
collection PubMed
description Haematopoietic stem cells (HSCs) are characterized by their self-renewal potential associated to dormancy. Here we identify the cell surface receptor neogenin-1 as specifically expressed in dormant HSCs. Loss of neogenin-1 initially leads to increased HSC expansion but subsequently to loss of self-renewal and premature exhaustion in vivo. Its ligand netrin-1 induces Egr1 expression and maintains quiescence and function of cultured HSCs in a Neo1 dependent manner. Produced by arteriolar endothelial and periarteriolar stromal cells, conditional netrin-1 deletion in the bone marrow niche reduces HSC numbers, quiescence and self-renewal, while overexpression increases quiescence in vivo. Ageing associated bone marrow remodelling leads to the decline of netrin-1 expression in niches and a compensatory but reversible upregulation of neogenin-1 on HSCs. Our study suggests that niche produced netrin-1 preserves HSC quiescence and self-renewal via neogenin-1 function. Decline of netrin-1 production during ageing leads to the gradual decrease of Neo1 mediated HSC self-renewal.
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spelling pubmed-78408072021-01-29 Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1 Renders, Simon Svendsen, Arthur Flohr Panten, Jasper Rama, Nicolas Maryanovich, Maria Sommerkamp, Pia Ladel, Luisa Redavid, Anna Rita Gibert, Benjamin Lazare, Seka Ducarouge, Benjamin Schönberger, Katharina Narr, Andreas Tourbez, Manon Dethmers-Ausema, Bertien Zwart, Erik Hotz-Wagenblatt, Agnes Zhang, Dachuan Korn, Claudia Zeisberger, Petra Przybylla, Adriana Sohn, Markus Mendez-Ferrer, Simon Heikenwälder, Mathias Brune, Maik Klimmeck, Daniel Bystrykh, Leonid Frenette, Paul S. Mehlen, Patrick de Haan, Gerald Cabezas-Wallscheid, Nina Trumpp, Andreas Nat Commun Article Haematopoietic stem cells (HSCs) are characterized by their self-renewal potential associated to dormancy. Here we identify the cell surface receptor neogenin-1 as specifically expressed in dormant HSCs. Loss of neogenin-1 initially leads to increased HSC expansion but subsequently to loss of self-renewal and premature exhaustion in vivo. Its ligand netrin-1 induces Egr1 expression and maintains quiescence and function of cultured HSCs in a Neo1 dependent manner. Produced by arteriolar endothelial and periarteriolar stromal cells, conditional netrin-1 deletion in the bone marrow niche reduces HSC numbers, quiescence and self-renewal, while overexpression increases quiescence in vivo. Ageing associated bone marrow remodelling leads to the decline of netrin-1 expression in niches and a compensatory but reversible upregulation of neogenin-1 on HSCs. Our study suggests that niche produced netrin-1 preserves HSC quiescence and self-renewal via neogenin-1 function. Decline of netrin-1 production during ageing leads to the gradual decrease of Neo1 mediated HSC self-renewal. Nature Publishing Group UK 2021-01-27 /pmc/articles/PMC7840807/ /pubmed/33504783 http://dx.doi.org/10.1038/s41467-020-20801-0 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Renders, Simon
Svendsen, Arthur Flohr
Panten, Jasper
Rama, Nicolas
Maryanovich, Maria
Sommerkamp, Pia
Ladel, Luisa
Redavid, Anna Rita
Gibert, Benjamin
Lazare, Seka
Ducarouge, Benjamin
Schönberger, Katharina
Narr, Andreas
Tourbez, Manon
Dethmers-Ausema, Bertien
Zwart, Erik
Hotz-Wagenblatt, Agnes
Zhang, Dachuan
Korn, Claudia
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Mendez-Ferrer, Simon
Heikenwälder, Mathias
Brune, Maik
Klimmeck, Daniel
Bystrykh, Leonid
Frenette, Paul S.
Mehlen, Patrick
de Haan, Gerald
Cabezas-Wallscheid, Nina
Trumpp, Andreas
Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title_full Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title_fullStr Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title_full_unstemmed Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title_short Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
title_sort niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7840807/
https://www.ncbi.nlm.nih.gov/pubmed/33504783
http://dx.doi.org/10.1038/s41467-020-20801-0
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