Your browser doesn't support javascript.
loading
The multifaceted functions of CXCL10 in cardiovascular disease.
van den Borne, Pleunie; Quax, Paul H A; Hoefer, Imo E; Pasterkamp, Gerard.
Afiliação
  • van den Borne P; Laboratory of Experimental Cardiology, University Medical Center Utrecht, P.O. Box 85500, 3508 GA, Utrecht, The Netherlands.
  • Quax PH; Department of Surgery, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The Netherlands ; Einthoven Laboratory of Experimental Vascular Medicine, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The Netherlands.
  • Hoefer IE; Laboratory of Experimental Cardiology, University Medical Center Utrecht, P.O. Box 85500, 3508 GA, Utrecht, The Netherlands ; Interuniversity Cardiology Institute of the Netherlands, P.O. Box 19258, 3501 DG, Utrecht, The Netherlands.
  • Pasterkamp G; Laboratory of Experimental Cardiology, University Medical Center Utrecht, P.O. Box 85500, 3508 GA, Utrecht, The Netherlands ; Interuniversity Cardiology Institute of the Netherlands, P.O. Box 19258, 3501 DG, Utrecht, The Netherlands.
Biomed Res Int ; 2014: 893106, 2014.
Article em En | MEDLINE | ID: mdl-24868552
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Regulação da Expressão Gênica / Quimiocina CXCL10 Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Biomed Res Int Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Regulação da Expressão Gênica / Quimiocina CXCL10 Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Biomed Res Int Ano de publicação: 2014 Tipo de documento: Article