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The hematopoietic stem-cell niche in health and leukemia

Research in the last decade has shown that hematopoietic stem cells (HSCs) interact with and are modulated by a complex multicellular microenvironment in the bone marrow, which includes both the HSC progeny and multiple non-hematopoietic cell types. Intense work is gradually throwing light on the co...

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Detalles Bibliográficos
Autores principales: Sánchez-Aguilera, Abel, Méndez-Ferrer, Simón
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5272896/
https://www.ncbi.nlm.nih.gov/pubmed/27436341
http://dx.doi.org/10.1007/s00018-016-2306-y
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author Sánchez-Aguilera, Abel
Méndez-Ferrer, Simón
author_facet Sánchez-Aguilera, Abel
Méndez-Ferrer, Simón
author_sort Sánchez-Aguilera, Abel
collection PubMed
description Research in the last decade has shown that hematopoietic stem cells (HSCs) interact with and are modulated by a complex multicellular microenvironment in the bone marrow, which includes both the HSC progeny and multiple non-hematopoietic cell types. Intense work is gradually throwing light on the composition of the HSC niche and the molecular cues exchanged between its components, which has implications for HSC production, maintenance and expansion. In addition, it has become apparent that bidirectional interactions between leukemic cells and their niche play a previously unrecognized role in the initiation and development of hematological malignancies. Consequently, targeting of the malignant niche holds considerable promise for more specific antileukemic therapies. Here we summarize the latest insights into HSC niche biology and recent work showing multiple connections between hematological malignancy and alterations in the bone marrow microenvironment.
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spelling pubmed-52728962017-02-10 The hematopoietic stem-cell niche in health and leukemia Sánchez-Aguilera, Abel Méndez-Ferrer, Simón Cell Mol Life Sci Review Research in the last decade has shown that hematopoietic stem cells (HSCs) interact with and are modulated by a complex multicellular microenvironment in the bone marrow, which includes both the HSC progeny and multiple non-hematopoietic cell types. Intense work is gradually throwing light on the composition of the HSC niche and the molecular cues exchanged between its components, which has implications for HSC production, maintenance and expansion. In addition, it has become apparent that bidirectional interactions between leukemic cells and their niche play a previously unrecognized role in the initiation and development of hematological malignancies. Consequently, targeting of the malignant niche holds considerable promise for more specific antileukemic therapies. Here we summarize the latest insights into HSC niche biology and recent work showing multiple connections between hematological malignancy and alterations in the bone marrow microenvironment. Springer International Publishing 2016-07-19 2017 /pmc/articles/PMC5272896/ /pubmed/27436341 http://dx.doi.org/10.1007/s00018-016-2306-y Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Review
Sánchez-Aguilera, Abel
Méndez-Ferrer, Simón
The hematopoietic stem-cell niche in health and leukemia
title The hematopoietic stem-cell niche in health and leukemia
title_full The hematopoietic stem-cell niche in health and leukemia
title_fullStr The hematopoietic stem-cell niche in health and leukemia
title_full_unstemmed The hematopoietic stem-cell niche in health and leukemia
title_short The hematopoietic stem-cell niche in health and leukemia
title_sort hematopoietic stem-cell niche in health and leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5272896/
https://www.ncbi.nlm.nih.gov/pubmed/27436341
http://dx.doi.org/10.1007/s00018-016-2306-y
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