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Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection

Inflammation is an evolutionarily selected defense response to infection or tissue damage that involves activation and consumption of immune cells in order to reestablish and maintain organismal integrity. In this process, hematopoietic stem cells (HSCs) are themselves exposed to inflammatory cues a...

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Detalles Bibliográficos
Autores principales: Caiado, Francisco, Pietras, Eric M., Manz, Markus G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210622/
https://www.ncbi.nlm.nih.gov/pubmed/34129016
http://dx.doi.org/10.1084/jem.20201541
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author Caiado, Francisco
Pietras, Eric M.
Manz, Markus G.
author_facet Caiado, Francisco
Pietras, Eric M.
Manz, Markus G.
author_sort Caiado, Francisco
collection PubMed
description Inflammation is an evolutionarily selected defense response to infection or tissue damage that involves activation and consumption of immune cells in order to reestablish and maintain organismal integrity. In this process, hematopoietic stem cells (HSCs) are themselves exposed to inflammatory cues and via proliferation and differentiation, replace mature immune cells in a demand-adapted fashion. Here, we review how major sources of systemic inflammation act on and subsequently shape HSC fate and function. We highlight how lifelong inflammatory exposure contributes to HSC inflamm-aging and selection of premalignant HSC clones. Finally, we explore emerging areas of interest and open questions remaining in the field.
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spelling pubmed-82106222022-01-05 Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection Caiado, Francisco Pietras, Eric M. Manz, Markus G. J Exp Med Review Inflammation is an evolutionarily selected defense response to infection or tissue damage that involves activation and consumption of immune cells in order to reestablish and maintain organismal integrity. In this process, hematopoietic stem cells (HSCs) are themselves exposed to inflammatory cues and via proliferation and differentiation, replace mature immune cells in a demand-adapted fashion. Here, we review how major sources of systemic inflammation act on and subsequently shape HSC fate and function. We highlight how lifelong inflammatory exposure contributes to HSC inflamm-aging and selection of premalignant HSC clones. Finally, we explore emerging areas of interest and open questions remaining in the field. Rockefeller University Press 2021-06-15 /pmc/articles/PMC8210622/ /pubmed/34129016 http://dx.doi.org/10.1084/jem.20201541 Text en © 2021 Caiado et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Review
Caiado, Francisco
Pietras, Eric M.
Manz, Markus G.
Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title_full Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title_fullStr Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title_full_unstemmed Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title_short Inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
title_sort inflammation as a regulator of hematopoietic stem cell function in disease, aging, and clonal selection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210622/
https://www.ncbi.nlm.nih.gov/pubmed/34129016
http://dx.doi.org/10.1084/jem.20201541
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