首页> 外文期刊>Journal of Cell Communication and Signaling >CCN3/NOV small interfering RNA enhances fibrogenic gene expression in primary hepatic stellate cells and cirrhotic fat storing cell line CFSC
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CCN3/NOV small interfering RNA enhances fibrogenic gene expression in primary hepatic stellate cells and cirrhotic fat storing cell line CFSC

机译:CCN3 / NOV小干扰RNA增强原代肝星状细胞和肝硬化储脂细胞系CFSC中纤维化基因的表达

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Nephroblastoma overexpressed gene encodes a matricellular protein (CCN3/NOV) of the CCN family, comprising CCN1 (CYR61), CCN2 (CTGF), CCN4 (WISP-1), CCN5 (WISP-2), and CCN6 (WISP-3). CCN proteins are involved in the regulation of mitosis, adhesion, apoptosis, extracellular matrix production, growth arrest and migration in multiple cell types. Compared to CCN2/CTGF, known as a profibrotic protein, the biological role of CCN3/NOV in liver fibrosis remains obscure. In this study we showed ccn3ov mRNA to increase dramatically following hepatic stellate cell activation, reaching peak levels in fully transdifferentiated myofibroblasts. In models of experimental hepatic fibrosis, CCN3/NOV increased significantly at the mRNA and protein levels. CCN3/NOV was found mainly in non-parenchymal cells along the areas of tissue damage and repair. In the bile-duct ligation model, CCN3/NOV was localized mainly along portal tracts, while the repeated application of carbon tetrachloride resulted in CCN3/NOV expression mainly in the centrilobular areas. In contrast to CCN2/CTGF, the profibrotic cytokines platelet-derived growth factor-B and -D as well as transforming growth factor-β suppressed CCN3/NOV expression. In vitro, CCN3/NOV siRNA attenuated migration in the cirrhotic fat storing cell line CFSC well in line with in vivo findings that various types of cells expressing CCN3/NOV migrate into the area of tissue damage and regeneration. The suppression of CCN3/NOV enhanced expression of profibrotic marker proteins, such as α-smooth muscle actin, collagen type I, fibronectin, CCN2/CTGF and TIMP-1 in primary rat hepatic stellate cells and in CFSC. We further found that adenoviral overexpression of CCN2/CTGF suppressed CCN3/NOV expression, while the overexpression of CCN3/NOV as well as the suppression of CCN3/NOV by targeting siRNAs both resulted in enhanced CCN2/CTGF expression. These results indicate the complexity of CCN actions that are far beyond the classic Yin/Yang interplay.
机译:肾母细胞瘤过表达的基因编码CCN家族的基质细胞蛋白(CCN3 / NOV),包括CCN1,CYR61,CCN2,CTGF,C4,WISP-1,C5,WISP-2和CCN6。 CCN蛋白参与多种细胞类型的有丝分裂,粘附,凋亡,细胞外基质产生,生长停滞和迁移的调节。与被称为纤维蛋白原的蛋白CCN2 / CTGF相比,CCN3 / NOV在肝纤维化中的生物学作用仍然不清楚。在这项研究中,我们显示ccn3 / nov mRNA在肝星状细胞激活后急剧增加,在完全转分化的成肌纤维细胞中达到峰值。在实验性肝纤维化模型中,CCN3 / NOV在mRNA和蛋白质水平上显着增加。 CCN3 / NOV主要在组织损伤和修复区域的非实质细胞中发现。在胆管结扎模型中,CCN3 / NOV主要定位在门脉,而四氯化碳的重复应用导致CCN3 / NOV的表达主要在小叶区域。与CCN2 / CTGF相比,原纤维化细胞因子血小板衍生的生长因子B和-D以及转化生长因子β抑制了CCN3​​ / NOV的表达。在体外,CCN3 / NOV siRNA很好地减弱了肝硬化储脂细胞系CFSC中的迁移,这与体内发现表达CCN3 / NOV的各种类型的细胞迁移到组织损伤和再生区域的体内发现一致。 CCN3 / NOV的抑制增强了原代大鼠肝星状细胞和CFSC中纤维化标记蛋白的表达,例如α-平滑肌肌动蛋白,I型胶原,纤连蛋白,CCN2 / CTGF和TIMP-1。我们进一步发现,腺病毒过表达CCN2 / CTGF抑制CCN3 / NOV表达,而过表达CCN3 / NOV以及通过靶向siRNA抑制CCN3 / NOV均导致CCN2 / CTGF表达增强。这些结果表明,CCN动作的复杂性远远超出了经典的阴/阳相互作用。

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