Cargando…
Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system
Innate and adaptive immune cells participate in the homeostatic regulation of hematopoietic stem cells (HSCs). Here, we interrogate the contribution of myeloid cells, the most abundant cell type in the mammalian bone marrow, in a clinically relevant mouse model of neutropenia. Long-term genetic depl...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741615/ https://www.ncbi.nlm.nih.gov/pubmed/36496394 http://dx.doi.org/10.1038/s41467-022-35318-x |
_version_ | 1784848363281186816 |
---|---|
author | Feyen, Jacqueline Ping, Zhen Chen, Lanpeng van Dijk, Claire van Tienhoven, Tim V. D. van Strien, Paulina M. H. Hoogenboezem, Remco M. Wevers, Michiel J. W. Sanders, Mathijs A. Touw, Ivo P. Raaijmakers, Marc H. G. P. |
author_facet | Feyen, Jacqueline Ping, Zhen Chen, Lanpeng van Dijk, Claire van Tienhoven, Tim V. D. van Strien, Paulina M. H. Hoogenboezem, Remco M. Wevers, Michiel J. W. Sanders, Mathijs A. Touw, Ivo P. Raaijmakers, Marc H. G. P. |
author_sort | Feyen, Jacqueline |
collection | PubMed |
description | Innate and adaptive immune cells participate in the homeostatic regulation of hematopoietic stem cells (HSCs). Here, we interrogate the contribution of myeloid cells, the most abundant cell type in the mammalian bone marrow, in a clinically relevant mouse model of neutropenia. Long-term genetic depletion of neutrophils and eosinophils results in activation of multipotent progenitors but preservation of HSCs. Depletion of myeloid cells abrogates HSC expansion, loss of serial repopulation and lymphoid reconstitution capacity and remodeling of HSC niches, features previously associated with hematopoietic aging. This is associated with mitigation of interferon signaling in both HSCs and their niches via reduction of NK cell number and activation. These data implicate myeloid cells in the functional decline of hematopoiesis, associated with activation of interferon signaling via a putative neutrophil-NK cell axis. Innate immunity may thus come at the cost of system deterioration through enhanced chronic inflammatory signaling to stem cells and their niches. |
format | Online Article Text |
id | pubmed-9741615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97416152022-12-12 Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system Feyen, Jacqueline Ping, Zhen Chen, Lanpeng van Dijk, Claire van Tienhoven, Tim V. D. van Strien, Paulina M. H. Hoogenboezem, Remco M. Wevers, Michiel J. W. Sanders, Mathijs A. Touw, Ivo P. Raaijmakers, Marc H. G. P. Nat Commun Article Innate and adaptive immune cells participate in the homeostatic regulation of hematopoietic stem cells (HSCs). Here, we interrogate the contribution of myeloid cells, the most abundant cell type in the mammalian bone marrow, in a clinically relevant mouse model of neutropenia. Long-term genetic depletion of neutrophils and eosinophils results in activation of multipotent progenitors but preservation of HSCs. Depletion of myeloid cells abrogates HSC expansion, loss of serial repopulation and lymphoid reconstitution capacity and remodeling of HSC niches, features previously associated with hematopoietic aging. This is associated with mitigation of interferon signaling in both HSCs and their niches via reduction of NK cell number and activation. These data implicate myeloid cells in the functional decline of hematopoiesis, associated with activation of interferon signaling via a putative neutrophil-NK cell axis. Innate immunity may thus come at the cost of system deterioration through enhanced chronic inflammatory signaling to stem cells and their niches. Nature Publishing Group UK 2022-12-10 /pmc/articles/PMC9741615/ /pubmed/36496394 http://dx.doi.org/10.1038/s41467-022-35318-x 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Feyen, Jacqueline Ping, Zhen Chen, Lanpeng van Dijk, Claire van Tienhoven, Tim V. D. van Strien, Paulina M. H. Hoogenboezem, Remco M. Wevers, Michiel J. W. Sanders, Mathijs A. Touw, Ivo P. Raaijmakers, Marc H. G. P. Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title | Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title_full | Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title_fullStr | Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title_full_unstemmed | Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title_short | Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
title_sort | myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741615/ https://www.ncbi.nlm.nih.gov/pubmed/36496394 http://dx.doi.org/10.1038/s41467-022-35318-x |
work_keys_str_mv | AT feyenjacqueline myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT pingzhen myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT chenlanpeng myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT vandijkclaire myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT vantienhoventimvd myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT vanstrienpaulinamh myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT hoogenboezemremcom myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT weversmichieljw myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT sandersmathijsa myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT touwivop myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem AT raaijmakersmarchgp myeloidcellspromoteinterferonsignalingassociateddeteriorationofthehematopoieticsystem |