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The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration

The CXCR4 receptor upon binding its ligands triggers multiple signaling pathways that orchestrate cell migration, hematopoiesis and cell homing, and retention in the bone marrow. However, CXCR4 also directly controls cell proliferation of non-hematopoietic cells. This review focuses on recent report...

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Autores principales: Bianchi, Marco E., Mezzapelle, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484992/
https://www.ncbi.nlm.nih.gov/pubmed/32983169
http://dx.doi.org/10.3389/fimmu.2020.02109
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author Bianchi, Marco E.
Mezzapelle, Rosanna
author_facet Bianchi, Marco E.
Mezzapelle, Rosanna
author_sort Bianchi, Marco E.
collection PubMed
description The CXCR4 receptor upon binding its ligands triggers multiple signaling pathways that orchestrate cell migration, hematopoiesis and cell homing, and retention in the bone marrow. However, CXCR4 also directly controls cell proliferation of non-hematopoietic cells. This review focuses on recent reports pointing to its pivotal role in tissue regeneration and stem cell activation, and discusses the connection to the known role of CXCR4 in promoting tumor growth. The mechanisms may be similar in all cases, since regeneration often recapitulates developmental processes, and cancer often exploits developmental pathways. Moreover, cell migration and cell proliferation appear to be downstream of the same signaling pathways. A deeper understanding of the complex signaling originating from CXCR4 is needed to exploit the opportunities to repair damaged organs safely and effectively.
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spelling pubmed-74849922020-09-24 The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration Bianchi, Marco E. Mezzapelle, Rosanna Front Immunol Immunology The CXCR4 receptor upon binding its ligands triggers multiple signaling pathways that orchestrate cell migration, hematopoiesis and cell homing, and retention in the bone marrow. However, CXCR4 also directly controls cell proliferation of non-hematopoietic cells. This review focuses on recent reports pointing to its pivotal role in tissue regeneration and stem cell activation, and discusses the connection to the known role of CXCR4 in promoting tumor growth. The mechanisms may be similar in all cases, since regeneration often recapitulates developmental processes, and cancer often exploits developmental pathways. Moreover, cell migration and cell proliferation appear to be downstream of the same signaling pathways. A deeper understanding of the complex signaling originating from CXCR4 is needed to exploit the opportunities to repair damaged organs safely and effectively. Frontiers Media S.A. 2020-08-28 /pmc/articles/PMC7484992/ /pubmed/32983169 http://dx.doi.org/10.3389/fimmu.2020.02109 Text en Copyright © 2020 Bianchi and Mezzapelle. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bianchi, Marco E.
Mezzapelle, Rosanna
The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title_full The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title_fullStr The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title_full_unstemmed The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title_short The Chemokine Receptor CXCR4 in Cell Proliferation and Tissue Regeneration
title_sort chemokine receptor cxcr4 in cell proliferation and tissue regeneration
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484992/
https://www.ncbi.nlm.nih.gov/pubmed/32983169
http://dx.doi.org/10.3389/fimmu.2020.02109
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