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Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review

Like all immune cells, macrophages do not act autonomously but in unison with other immune cells, surrounding tissues, and the niche they occupy. Constant exchange of information between cellular and noncellular participants within a tissue allows for preserving homeostasis and defining responses in...

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Autores principales: Kloc, Malgorzata, Uosef, Ahmed, Ubelaker, Henry V., Kubiak, Jacek Z., Ghobrial, Rafik M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107080/
https://www.ncbi.nlm.nih.gov/pubmed/37077316
http://dx.doi.org/10.21037/sci-2023-009
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author Kloc, Malgorzata
Uosef, Ahmed
Ubelaker, Henry V.
Kubiak, Jacek Z.
Ghobrial, Rafik M.
author_facet Kloc, Malgorzata
Uosef, Ahmed
Ubelaker, Henry V.
Kubiak, Jacek Z.
Ghobrial, Rafik M.
author_sort Kloc, Malgorzata
collection PubMed
description Like all immune cells, macrophages do not act autonomously but in unison with other immune cells, surrounding tissues, and the niche they occupy. Constant exchange of information between cellular and noncellular participants within a tissue allows for preserving homeostasis and defining responses in a pathologic environment. Although molecular mechanisms and pathways involved in reciprocal signaling between macrophages and other immune cells have been known for decades, much less is known about interactions between macrophages and stem/progenitor cells. Based on the time when stem cells form, there are two stem cell types: embryonic stem cells existing only in an early embryo, which are pluripotent and can differentiate into any cell type present in an adult, and somatic (adult) stem cells formed in fetus and persisting for whole adult life. Tissues and organs have their own (tissue-specific and organ-specific) adult stem cells, which serve as a reserve for tissue homeostasis and regeneration after injury. It is still uncertain whether organ- and tissue-specific stem cells are actual stem cells or just progenitor cells. The important question is how stem/progenitor cells can sculpt macrophage phenotype and functions. Even less is known if or how macrophages can shape stem/progenitor cell functions, their divisions, and fate. We describe here examples from recent studies of how stem/progenitor cells can affect macrophages and how macrophages can influence stem/progenitor cell properties, functions, and destiny.
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spelling pubmed-101070802023-04-18 Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review Kloc, Malgorzata Uosef, Ahmed Ubelaker, Henry V. Kubiak, Jacek Z. Ghobrial, Rafik M. Stem Cell Investig Review Article Like all immune cells, macrophages do not act autonomously but in unison with other immune cells, surrounding tissues, and the niche they occupy. Constant exchange of information between cellular and noncellular participants within a tissue allows for preserving homeostasis and defining responses in a pathologic environment. Although molecular mechanisms and pathways involved in reciprocal signaling between macrophages and other immune cells have been known for decades, much less is known about interactions between macrophages and stem/progenitor cells. Based on the time when stem cells form, there are two stem cell types: embryonic stem cells existing only in an early embryo, which are pluripotent and can differentiate into any cell type present in an adult, and somatic (adult) stem cells formed in fetus and persisting for whole adult life. Tissues and organs have their own (tissue-specific and organ-specific) adult stem cells, which serve as a reserve for tissue homeostasis and regeneration after injury. It is still uncertain whether organ- and tissue-specific stem cells are actual stem cells or just progenitor cells. The important question is how stem/progenitor cells can sculpt macrophage phenotype and functions. Even less is known if or how macrophages can shape stem/progenitor cell functions, their divisions, and fate. We describe here examples from recent studies of how stem/progenitor cells can affect macrophages and how macrophages can influence stem/progenitor cell properties, functions, and destiny. AME Publishing Company 2023-04-13 /pmc/articles/PMC10107080/ /pubmed/37077316 http://dx.doi.org/10.21037/sci-2023-009 Text en 2023 Stem Cell Investigation. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Article
Kloc, Malgorzata
Uosef, Ahmed
Ubelaker, Henry V.
Kubiak, Jacek Z.
Ghobrial, Rafik M.
Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title_full Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title_fullStr Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title_full_unstemmed Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title_short Macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
title_sort macrophages and stem/progenitor cells interplay in adipose tissue and skeletal muscle: a review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107080/
https://www.ncbi.nlm.nih.gov/pubmed/37077316
http://dx.doi.org/10.21037/sci-2023-009
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