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The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in

Stem cell niches are defined as the cellular and molecular microenvironments that regulate stem cell function together with stem cell autonomous mechanisms. This includes control of the balance between quiescence, self-renewal, and differentiation, as well as the engagement of specific programs in r...

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Detalles Bibliográficos
Autores principales: Ehninger, Armin, Trumpp, Andreas
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058583/
https://www.ncbi.nlm.nih.gov/pubmed/21402747
http://dx.doi.org/10.1084/jem.20110132
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author Ehninger, Armin
Trumpp, Andreas
author_facet Ehninger, Armin
Trumpp, Andreas
author_sort Ehninger, Armin
collection PubMed
description Stem cell niches are defined as the cellular and molecular microenvironments that regulate stem cell function together with stem cell autonomous mechanisms. This includes control of the balance between quiescence, self-renewal, and differentiation, as well as the engagement of specific programs in response to stress. In mammals, the best understood niche is that harboring bone marrow hematopoietic stem cells (HSCs). Recent studies have expanded the number of cell types contributing to the HSC niche. Perivascular mesenchymal stem cells and macrophages now join the previously identified sinusoidal endothelial cells, sympathetic nerve fibers, and cells of the osteoblastic lineage to form similar, but distinct, niches that harbor dormant and self-renewing HSCs during homeostasis and mediate stem cell mobilization in response to granulocyte colony-stimulating factor.
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spelling pubmed-30585832011-09-14 The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in Ehninger, Armin Trumpp, Andreas J Exp Med Review Stem cell niches are defined as the cellular and molecular microenvironments that regulate stem cell function together with stem cell autonomous mechanisms. This includes control of the balance between quiescence, self-renewal, and differentiation, as well as the engagement of specific programs in response to stress. In mammals, the best understood niche is that harboring bone marrow hematopoietic stem cells (HSCs). Recent studies have expanded the number of cell types contributing to the HSC niche. Perivascular mesenchymal stem cells and macrophages now join the previously identified sinusoidal endothelial cells, sympathetic nerve fibers, and cells of the osteoblastic lineage to form similar, but distinct, niches that harbor dormant and self-renewing HSCs during homeostasis and mediate stem cell mobilization in response to granulocyte colony-stimulating factor. The Rockefeller University Press 2011-03-14 /pmc/articles/PMC3058583/ /pubmed/21402747 http://dx.doi.org/10.1084/jem.20110132 Text en © 2011 Ehninger and Trumpp 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Review
Ehninger, Armin
Trumpp, Andreas
The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title_full The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title_fullStr The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title_full_unstemmed The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title_short The bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
title_sort bone marrow stem cell niche grows up: mesenchymal stem cells and macrophages move in
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058583/
https://www.ncbi.nlm.nih.gov/pubmed/21402747
http://dx.doi.org/10.1084/jem.20110132
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