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Communication between bone marrow niches in normal bone marrow function and during hemopathies progression

Hematopoietic stem cell (HSC) chemotaxis, adhesion, proliferation, quiescence and differentiation are regulated by interactions with bone marrow (BM) niches. Two niches have been identified in the adult BM: the endosteal (close to the bone) and the perivascular niche (close to blood vessels). A vast...

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Detalles Bibliográficos
Autores principales: Lamorte, Sara, Remédio, Leonor, Dias, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222253/
http://dx.doi.org/10.4081/hr.2009.e14
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author Lamorte, Sara
Remédio, Leonor
Dias, Sergio
author_facet Lamorte, Sara
Remédio, Leonor
Dias, Sergio
author_sort Lamorte, Sara
collection PubMed
description Hematopoietic stem cell (HSC) chemotaxis, adhesion, proliferation, quiescence and differentiation are regulated by interactions with bone marrow (BM) niches. Two niches have been identified in the adult BM: the endosteal (close to the bone) and the perivascular niche (close to blood vessels). A vast body of literature has revealed the molecular basis for the interaction of HSCs with the two niches. However, the signals that regulate the communication between the two niches have not been well defined. Taking in consideration several clinical and experimental arguments this review highlights the molecular cues, involved in the communication between the BM niches, which regulate the basic properties of HSCs in physiological and malignant conditions. As such, it aims at clarifying the most important advances in basic and clinical research focusing on the role of different factors in the regulation of the BM microenvironment.
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spelling pubmed-32222532011-12-19 Communication between bone marrow niches in normal bone marrow function and during hemopathies progression Lamorte, Sara Remédio, Leonor Dias, Sergio Hematol Rev Article Hematopoietic stem cell (HSC) chemotaxis, adhesion, proliferation, quiescence and differentiation are regulated by interactions with bone marrow (BM) niches. Two niches have been identified in the adult BM: the endosteal (close to the bone) and the perivascular niche (close to blood vessels). A vast body of literature has revealed the molecular basis for the interaction of HSCs with the two niches. However, the signals that regulate the communication between the two niches have not been well defined. Taking in consideration several clinical and experimental arguments this review highlights the molecular cues, involved in the communication between the BM niches, which regulate the basic properties of HSCs in physiological and malignant conditions. As such, it aims at clarifying the most important advances in basic and clinical research focusing on the role of different factors in the regulation of the BM microenvironment. PAGEPress Publications 2009-08-28 /pmc/articles/PMC3222253/ http://dx.doi.org/10.4081/hr.2009.e14 Text en ©Copyright S. Lamorte et al., 2009 This work is licensed under a Creative Commons Attribution 3.0 License (by-nc 3.0) Licensee PAGEPress, Italy
spellingShingle Article
Lamorte, Sara
Remédio, Leonor
Dias, Sergio
Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title_full Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title_fullStr Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title_full_unstemmed Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title_short Communication between bone marrow niches in normal bone marrow function and during hemopathies progression
title_sort communication between bone marrow niches in normal bone marrow function and during hemopathies progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222253/
http://dx.doi.org/10.4081/hr.2009.e14
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