Xue Bin, Li Fan-Chi, Tian Jiang-Hai, Li Jin-Xin, Cheng Xiao-Yu, Hu Jia-Huan, Hu Jing-Sheng, Li Bing
School of Basic Medicine and Biological Sciences, Soochow University, Suzhou, P.R. China.
National Engineering Laboratory for Modern Silk, Soochow University, Suzhou, P.R. China.
Arch Insect Biochem Physiol. 2018 Sep;99(1):e21470. doi: 10.1002/arch.21470. Epub 2018 Apr 30.
Various nanoparticles, such as silver nanoparticles (AgNPs) and titanium nanoparticles (TiO NPs) are increasingly used in industrial processes. Because they are released into the environment, research into their influence on the biosphere is necessary. Among its other effects, dietary TiO NPs promotes silk protein synthesis in silkworms, which prompted our hypothesis that TiO NPs influence protein kinase B (Akt)/Target of rapamycin (Tor) signaling pathway (Akt/Tor) signaling in their silk glands. The Akt/Tor signaling pathway is a principle connector integrating cellular reactions to growth factors, metabolites, nutrients, protein synthesis, and stress. We tested our hypothesis by determining the influence of dietary TiO NPs (for 72 h) and, separately, of two Akt/Tor pathway inhibitors (LY294002 and rapamycin) on expression of Akt/Tor signaling pathway genes and proteins in the silk glands. TiO NPs treatments led to increased accumulation of mRNAs for Akt, Tor1 and Tor2 by 1.6-, 12.1-, and 4.8-fold. Dietary inhibitors led to 2.6- to 4-fold increases in mRNAs encoding Akt and substantial decreases in mRNAs encoding Tor1 and Tor2. Western blot analysis showed that dietary TiO NPs increased the phosphorylation of Akt and its downstream proteins. LY294002 treatments led to inhibition of Akt phosphorylation and its downstream proteins and rapamycin treatments similarly inhibited the phosphorylation of Tor-linked downstream proteins. These findings support our hypothesis that TiO NPs influence Akt/Tor signaling in silk glands. The significance of this work is identification of specific sites of TiO NPs actions.
各种纳米颗粒,如银纳米颗粒(AgNPs)和钛纳米颗粒(TiO NPs)越来越多地用于工业生产过程中。由于它们会释放到环境中,因此有必要研究它们对生物圈的影响。除了其他作用外,经口摄入的TiO NPs可促进家蚕丝蛋白的合成,这促使我们提出一个假设,即TiO NPs会影响家蚕丝腺中的蛋白激酶B(Akt)/雷帕霉素靶蛋白(Tor)信号通路(Akt/Tor)信号。Akt/Tor信号通路是整合细胞对生长因子、代谢物、营养物质、蛋白质合成和应激反应的主要连接途径。我们通过测定经口摄入TiO NPs(72小时)以及分别使用两种Akt/Tor通路抑制剂(LY294002和雷帕霉素)对丝腺中Akt/Tor信号通路基因和蛋白质表达的影响来验证我们的假设。TiO NPs处理导致Akt、Tor1和Tor2的mRNA积累分别增加了1.6倍、12.1倍和4.8倍。经口摄入抑制剂导致编码Akt的mRNA增加2.6至4倍,而编码Tor1和Tor2的mRNA大幅减少。蛋白质免疫印迹分析表明,经口摄入TiO NPs可增加Akt及其下游蛋白的磷酸化。LY294002处理导致Akt磷酸化及其下游蛋白受到抑制,雷帕霉素处理同样抑制了与Tor相关的下游蛋白的磷酸化。这些发现支持了我们的假设,即TiO NPs会影响丝腺中的Akt/Tor信号。这项工作的意义在于确定了TiO NPs作用的特定部位。