Department of Cell Biology, Division of Host Defense Mechanism, Tokai University School of Medicine , 143 Shimokasuya, Isehara, Kanagawa 259-1193, Japan.
School of Bioscience and Biotechnology, Tokyo University of Technology , 1404-1 Katakura-cho, Hachioji, Tokyo 192-0982, Japan.
Acta Histochem Cytochem. 2014;47(5):185-94. doi: 10.1267/ahc.14030. Epub 2014 Sep 2.
Since there is a report that an inhibitor of protein kinase C (PKC) effectively suppresses the development of hepatic fibrosis, it is suggested that the PKC signaling pathway plays an important role in the pathogenesis of hepatic fibrosis. We reported that oxidized diacylglycerol (DAG), which is an activator of PKC, had a remarkably stronger PKC-activating action than un-oxidized DAG. In the present study, we explored the roles of oxidized DAG in hepatic fibrogenesis using mice, the livers of which developed fibrosis by long-term administration of carbon tetrachloride (CCl4). Liver fibrosis models were created by 4- or 8-week repetitive subcutaneous injections of CCl4 to the backs of C57BL/6J mice. The amount of oxidized DAG was significantly increased in the CCl4-treated group. Moreover, it was found that PKCα, βI, βII and δ were activated. In the CCl4-treated group, phosphorylation of ERK and JNK, which are downstream signal transmitters in the PKC pathway, was increased. It was also found in this group that there was an increase in TIMP-1, which is a fibrogenesis-promoting factor whose expression is enhanced by activated JNK, and of TNF-α, an inflammatory cytokine. Analysis by quantitative real-time RT-PCR showed that expressions of αSMA, collagen I, TNF-α and IL-10 were remarkably increased in the 8-week CCl4-treated group. The above results strongly suggested that oxidized DAG, which is increased by augmented oxidative stress, activated PKCα, βI, βII and δ molecular species and that these molecular species in turn stimulated the phosphorylation of MAP kinases including ERK and JNK, resulting in enhancement of hepatic fibrogenesis.
由于有报道称蛋白激酶 C(PKC)抑制剂能有效抑制肝纤维化的发展,这表明 PKC 信号通路在肝纤维化发病机制中起着重要作用。我们曾报道过,氧化二酰基甘油(DAG)作为 PKC 的激活剂,其激活 PKC 的作用比未氧化的 DAG 强得多。在本研究中,我们使用 CCl4 长期给药诱导肝纤维化的小鼠模型来探讨氧化 DAG 在肝纤维化中的作用。4 或 8 周时,通过背部皮下重复注射 CCl4 建立肝纤维化模型。CCl4 处理组中氧化 DAG 的含量明显增加。此外,还发现 PKCα、βI、βII 和 δ 被激活。在 CCl4 处理组中,PKC 途径下游信号转导分子 ERK 和 JNK 的磷酸化增加。还发现促纤维化因子 TIMP-1 和炎症细胞因子 TNF-α的表达增加,TIMP-1 的表达增强是由 JNK 激活引起的。定量实时 RT-PCR 分析显示,在 8 周 CCl4 处理组中,αSMA、胶原 I、TNF-α和 IL-10 的表达显著增加。上述结果强烈表明,氧化应激增强导致氧化 DAG 增加,激活了 PKCα、βI、βII 和 δ 分子亚型,这些分子亚型反过来又刺激了包括 ERK 和 JNK 在内的 MAP 激酶的磷酸化,从而增强了肝纤维化的发生。