Sato Junya, Kinugasa Mitsuo, Satomi-Kobayashi Seimi, Hatakeyama Kinta, Knox Aaron J, Asada Yujiro, Wierman Margaret E, Hirata Ken-ichi, Rikitake Yoshiyuki
Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.
Department of Pathology, Faculty of Medicine, University of Miyazaki, Miyazaki, Miyazaki, Japan.
PLoS One. 2014 Sep 24;9(9):e107236. doi: 10.1371/journal.pone.0107236. eCollection 2014.
Identification of the regulators of vascular inflammation is important if we are to understand the molecular mechanisms leading to atherosclerosis and consequent ischemic heart disease, including acute myocardial infarction. Gene polymorphisms in family with sequence similarity 5, member C (FAM5C) are associated with an increased risk of acute myocardial infarction, but little is known about the function of this gene product in blood vessels. Here, we report that the regulation of the expression and function of FAM5C in endothelial cells. We show here that FAM5C is expressed in endothelial cells in vitro and in vivo. Immunofluorescence microscopy showed localization of FAM5C in the Golgi in cultured human endothelial cells. Immunohistochemistry on serial sections of human coronary artery showed that FAM5C-positive endothelium expressed intercellular adhesion molecule-1 (ICAM-1) or vascular cell adhesion molecule-1 (VCAM-1). In cultured human endothelial cells, the overexpression of FAM5C increased the reactive oxygen species (ROS) production, nuclear factor-κB (NF-κB) activity and the expression of ICAM-1, VCAM-1 and E-selectin mRNAs, resulting in enhanced monocyte adhesion. FAM5C was upregulated in response to inflammatory stimuli, such as TNF-α, in an NF-κB- and JNK-dependent manner. Knockdown of FAM5C by small interfering RNA inhibited the increase in the TNF-α-induced production of ROS, NF-κB activity and expression of these leukocyte adhesion molecule mRNAs, resulting in reduced monocyte adhesion. These results suggest that in endothelial cells, when FAM5C is upregulated in response to inflammatory stimuli, it increases the expression of leukocyte adhesion molecules by increasing ROS production and NF-κB activity.
如果我们想要了解导致动脉粥样硬化及随之而来的缺血性心脏病(包括急性心肌梗死)的分子机制,识别血管炎症的调节因子就很重要。序列相似性家族5成员C(FAM5C)基因多态性与急性心肌梗死风险增加相关,但关于该基因产物在血管中的功能却知之甚少。在此,我们报告了内皮细胞中FAM5C表达及功能的调节情况。我们发现FAM5C在体外和体内的内皮细胞中均有表达。免疫荧光显微镜显示,在培养的人内皮细胞中FAM5C定位于高尔基体。对人冠状动脉连续切片进行免疫组织化学分析表明,FAM5C阳性内皮表达细胞间黏附分子-1(ICAM-1)或血管细胞黏附分子-1(VCAM-1)。在培养的人内皮细胞中,FAM5C过表达增加了活性氧(ROS)生成、核因子-κB(NF-κB)活性以及ICAM-1、VCAM-1和E-选择素mRNA的表达,导致单核细胞黏附增强。FAM5C以NF-κB和JNK依赖的方式响应炎症刺激(如TNF-α)而上调。用小干扰RNA敲低FAM5C可抑制TNF-α诱导的ROS生成增加、NF-κB活性以及这些白细胞黏附分子mRNA的表达,从而减少单核细胞黏附。这些结果表明,在内皮细胞中,当FAM5C响应炎症刺激而上调时,它通过增加ROS生成和NF-κB活性来增加白细胞黏附分子的表达。