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The Multifaceted Functions of CXCL10 in Cardiovascular Disease
C-X-C motif ligand 10 (CXCL10), or interferon-inducible protein-10, is a small chemokine belonging to the CXC chemokine family. Its members are responsible for leukocyte trafficking and act on tissue cells, like endothelial and vascular smooth muscle cells. CXCL10 is secreted by leukocytes and tissu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017714/ https://www.ncbi.nlm.nih.gov/pubmed/24868552 http://dx.doi.org/10.1155/2014/893106 |
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author | van den Borne, Pleunie Quax, Paul H. A. Hoefer, Imo E. Pasterkamp, Gerard |
author_facet | van den Borne, Pleunie Quax, Paul H. A. Hoefer, Imo E. Pasterkamp, Gerard |
author_sort | van den Borne, Pleunie |
collection | PubMed |
description | C-X-C motif ligand 10 (CXCL10), or interferon-inducible protein-10, is a small chemokine belonging to the CXC chemokine family. Its members are responsible for leukocyte trafficking and act on tissue cells, like endothelial and vascular smooth muscle cells. CXCL10 is secreted by leukocytes and tissue cells and functions as a chemoattractant, mainly for lymphocytes. After binding to its receptor CXCR3, CXCL10 evokes a range of inflammatory responses: key features in cardiovascular disease (CVD). The role of CXCL10 in CVD has been extensively described, for example for atherosclerosis, aneurysm formation, and myocardial infarction. However, there seems to be a discrepancy between experimental and clinical settings. This discrepancy occurs from differences in biological actions between species (e.g. mice and human), which is dependent on CXCL10 signaling via different CXCR3 isoforms or CXCR3-independent signaling. This makes translation from experimental to clinical settings challenging. Furthermore, the overall consensus on the actions of CXCL10 in specific CVD models is not yet reached. The purpose of this review is to describe the functions of CXCL10 in different CVDs in both experimental and clinical settings and to highlight and discuss the possible discrepancies and translational difficulties. Furthermore, CXCL10 as a possible biomarker in CVD will be discussed. |
format | Online Article Text |
id | pubmed-4017714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40177142014-05-27 The Multifaceted Functions of CXCL10 in Cardiovascular Disease van den Borne, Pleunie Quax, Paul H. A. Hoefer, Imo E. Pasterkamp, Gerard Biomed Res Int Review Article C-X-C motif ligand 10 (CXCL10), or interferon-inducible protein-10, is a small chemokine belonging to the CXC chemokine family. Its members are responsible for leukocyte trafficking and act on tissue cells, like endothelial and vascular smooth muscle cells. CXCL10 is secreted by leukocytes and tissue cells and functions as a chemoattractant, mainly for lymphocytes. After binding to its receptor CXCR3, CXCL10 evokes a range of inflammatory responses: key features in cardiovascular disease (CVD). The role of CXCL10 in CVD has been extensively described, for example for atherosclerosis, aneurysm formation, and myocardial infarction. However, there seems to be a discrepancy between experimental and clinical settings. This discrepancy occurs from differences in biological actions between species (e.g. mice and human), which is dependent on CXCL10 signaling via different CXCR3 isoforms or CXCR3-independent signaling. This makes translation from experimental to clinical settings challenging. Furthermore, the overall consensus on the actions of CXCL10 in specific CVD models is not yet reached. The purpose of this review is to describe the functions of CXCL10 in different CVDs in both experimental and clinical settings and to highlight and discuss the possible discrepancies and translational difficulties. Furthermore, CXCL10 as a possible biomarker in CVD will be discussed. Hindawi Publishing Corporation 2014 2014-04-23 /pmc/articles/PMC4017714/ /pubmed/24868552 http://dx.doi.org/10.1155/2014/893106 Text en Copyright © 2014 Pleunie van den Borne et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article van den Borne, Pleunie Quax, Paul H. A. Hoefer, Imo E. Pasterkamp, Gerard The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title | The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title_full | The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title_fullStr | The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title_full_unstemmed | The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title_short | The Multifaceted Functions of CXCL10 in Cardiovascular Disease |
title_sort | multifaceted functions of cxcl10 in cardiovascular disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017714/ https://www.ncbi.nlm.nih.gov/pubmed/24868552 http://dx.doi.org/10.1155/2014/893106 |
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