Katsarou Konstantina, Tsitoura Panagiota, Georgopoulou Urania
Molecular Virology Laboratory, Hellenic Pasteur Institute, Greece.
Biochim Biophys Acta. 2011 Oct;1813(10):1854-62. doi: 10.1016/j.bbamcr.2011.06.015. Epub 2011 Jul 8.
Hepatitis C virus (HCV) is an RNA positive strand virus, member of the Flaviviridae family. The viral particle is composed of a capsid containing the genome, surrounded by E1 and E2 proteins, however different forms of viral particles have been observed including non-enveloped particles. Previous reports have proposed that hepatitis C non-enveloped capsid-like particles (HCVne) enter cells of hepatic origin via clathrin-mediated endocytosis, during which different signaling events occur. In this report we show that HCVne particles are capable of inducing the recently discovered ERK5 pathway, in a dose dependent way. The ERK5 pathway can be activated by growth factors and other extracellular signals. This specific activation occurs through a well characterized upstream kinase, MEK5, and is capable of inducing gene regulation of mef2. In contrast, when HCV core structural and NS5A non-structural proteins were expressed endogenously no activation of this pathway was detected. These cell signaling events could be of critical importance and might give clues for the elucidation of cellular manifestations associated with HCV infection.
丙型肝炎病毒(HCV)是一种正链RNA病毒,属于黄病毒科。病毒粒子由包含基因组的衣壳组成,周围环绕着E1和E2蛋白,不过已观察到病毒粒子的不同形式,包括无包膜粒子。先前的报告提出,丙型肝炎无包膜衣壳样颗粒(HCVne)通过网格蛋白介导的内吞作用进入肝源性细胞,在此过程中会发生不同的信号转导事件。在本报告中,我们表明HCVne颗粒能够以剂量依赖的方式诱导最近发现的ERK5途径。ERK5途径可被生长因子和其他细胞外信号激活。这种特异性激活通过一个特征明确的上游激酶MEK5发生,并能够诱导mef2的基因调控。相比之下,当内源性表达HCV核心结构蛋白和NS5A非结构蛋白时,未检测到该途径的激活。这些细胞信号转导事件可能至关重要,并可能为阐明与HCV感染相关的细胞表现提供线索。