van den Borne Pleunie, Quax Paul H A, Hoefer Imo E, Pasterkamp Gerard
Laboratory of Experimental Cardiology, University Medical Center Utrecht, P.O. Box 85500, 3508 GA, Utrecht, The Netherlands.
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.
Biomed Res Int. 2014;2014:893106. doi: 10.1155/2014/893106. Epub 2014 Apr 23.
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.
C-X-C基序配体10(CXCL10),即干扰素诱导蛋白10,是一种属于CXC趋化因子家族的小分子趋化因子。其成员负责白细胞的迁移,并作用于组织细胞,如内皮细胞和血管平滑肌细胞。CXCL10由白细胞和组织细胞分泌,主要作为淋巴细胞的趋化因子发挥作用。与受体CXCR3结合后,CXCL10会引发一系列炎症反应:这些都是心血管疾病(CVD)的关键特征。CXCL10在心血管疾病中的作用已得到广泛描述,例如在动脉粥样硬化、动脉瘤形成和心肌梗死方面。然而,实验和临床环境之间似乎存在差异。这种差异源于不同物种(如小鼠和人类)之间生物学作用的不同,这取决于通过不同CXCR3亚型的CXCL10信号传导或不依赖CXCR3的信号传导。这使得从实验环境向临床环境的转化具有挑战性。此外,对于CXCL10在特定心血管疾病模型中的作用尚未达成总体共识。本综述的目的是描述CXCL10在实验和临床环境中不同心血管疾病中的功能,并突出和讨论可能存在的差异及转化困难。此外,还将讨论CXCL10作为心血管疾病中一种可能的生物标志物的情况。