Manea Simona-Adriana, Todirita Andra, Manea Adrian
Institute of Cellular Biology and Pathology 'Nicolae Simionescu' of the Romanian Academy, Bucharest, Romania.
PLoS One. 2013 Dec 23;8(12):e84170. doi: 10.1371/journal.pone.0084170. eCollection 2013.
High glucose-induced endothelial dysfunction is partially mediated by the down-stream pathophysiological effects triggered by increased expression of endothelin-1 (ET-1). The molecular control mechanisms of ET-1 synthesis are yet to be discovered. Members of the CCAAT/enhancer-binding proteins (C/EBP) family are important regulators of key metabolic processes, cellular differentiation and proinflammatory genes. In this study, we aimed at elucidating the role of C/EBP in mediating the high glucose effect on ET-1 expression in human endothelial cells (EC). Human umbilical vein cells (EAhy926) and primary cultures of human aortic EC were exposed to high levels of glucose (16.5-25 mM). Real-time PCR, Western blot, enzyme-linked immunosorbent assay, ET-1 promoter-luciferase reporter analysis, and chromatin immunoprecipitation assays were employed to investigate ET-1 regulation. High glucose activated C/EBPα, C/EBPβ, and C/EBPδ in a dose-dependent manner. It also promoted significant increases in ET-1 gene and peptide expression. Chemical inhibition of JNK, p38MAPK and ERK1/2 diminished significantly the high glucose-induced nuclear translocation of C/EBP and ET-1 expression. Silencing of C/EBPα, C/EBPβ or C/EBPδ greatly reduced the high glucose-induced upregulation of ET-1 mRNA, pre-pro-ET-1, and ET-1 secretion. The expression of various C/EBP isoforms was selectively downregulated by siRNA-mediated gene silencing. In silico analysis indicated the existence of typical C/EBP elements within human ET-1 gene promoter. Transient overexpression of C/EBPα, C/EBPβ or C/EBPδ upregulated the luciferase level controlled by the ET-1 gene promoter. The direct interaction of C/EBPα, C/EBPβ or C/EBPδ proteins with the ET-1 promoter in high glucose-exposed EC was confirmed by chromatin immunoprecipitation assay. High glucose-induced ET-1 expression is mediated through multiple mechanisms. We present evidence that members of the C/EBP proinflammatory transcription factors are important regulators of ET-1 in high glucose-exposed human endothelial cells. High glucose-induced activation of C/EBP-related signaling pathways may induce excessive ET-1 synthesis, thus promoting vasoconstriction and dysfunction of the vascular wall cells in diabetes.
高糖诱导的内皮功能障碍部分是由内皮素-1(ET-1)表达增加引发的下游病理生理效应介导的。ET-1合成的分子控制机制尚未被发现。CCAAT/增强子结合蛋白(C/EBP)家族成员是关键代谢过程、细胞分化和促炎基因的重要调节因子。在本研究中,我们旨在阐明C/EBP在介导高糖对人内皮细胞(EC)中ET-1表达的影响中的作用。人脐静脉细胞(EAhy926)和人主动脉EC原代培养物暴露于高水平葡萄糖(16.5 - 25 mM)。采用实时PCR、蛋白质印迹法、酶联免疫吸附测定、ET-1启动子-荧光素酶报告基因分析和染色质免疫沉淀测定来研究ET-1的调控。高糖以剂量依赖的方式激活C/EBPα、C/EBPβ和C/EBPδ。它还显著促进ET-1基因和肽表达的增加。对JNK、p38MAPK和ERK1/2的化学抑制显著降低了高糖诱导的C/EBP核转位和ET-1表达。C/EBPα、C/EBPβ或C/EBPδ的沉默大大降低了高糖诱导的ET-1 mRNA、前体-前ET-1和ET-1分泌的上调。通过siRNA介导的基因沉默选择性地下调了各种C/EBP异构体的表达。计算机分析表明人ET-1基因启动子内存在典型的C/EBP元件。C/EBPα、C/EBPβ或C/EBPδ的瞬时过表达上调了由ET-1基因启动子控制的荧光素酶水平。染色质免疫沉淀测定证实了在高糖暴露的EC中C/EBPα、C/EBPβ或C/EBPδ蛋白与ET-1启动子的直接相互作用。高糖诱导的ET-1表达是通过多种机制介导的。我们提供的证据表明,C/EBP促炎转录因子家族成员是高糖暴露的人内皮细胞中ET-1的重要调节因子。高糖诱导的C/EBP相关信号通路的激活可能诱导ET-1过度合成,从而促进糖尿病患者的血管收缩和血管壁细胞功能障碍。