The United Graduate School of Agricultural Sciences, Kagoshima University, Kagoshima, 890-0065, Japan.
Department of Applied Biological Sciences, Saga University, Saga, 840-8502, Japan.
Insect Biochem Mol Biol. 2018 Jun;97:19-30. doi: 10.1016/j.ibmb.2018.04.002. Epub 2018 Apr 19.
Growth-blocking peptide (GBP) and stress-responsive peptide (SRP) are insect cytokines whose expression levels are elevated by various stressful conditions such as parasitization and high or low temperatures. Both GBP and SRP are synthesized as precursors and released into the hemolymph, where they are enzymatically processed to active peptides. Injection of active GBP or SRP into early last instar larvae elicits a reduction in feeding and consequent growth retardation in the armyworm Mythimna separata. Although such functions are thought to benefit insects under stressful conditions by affecting their physiologies and behaviors, the relationship between GBP and SRP remains elusive. Here we show that heat stress-induced reactive oxygen species (ROS) elevated hemolymph GBP, which activated SRP transcription and increased the SRP concentration in the hemolymph. Injection of both GBP and SRP elevated hemolymph antioxidant levels. We found that simultaneous increases in both active cytokines occurred in the larval hemolymph from 2 to 3 h after heat stress or HO injection, suggesting a synergic action of the two factors. This speculation was confirmed by demonstrating that co-injection of GBP and SRP caused a more severe reduction in appetite and growth retardation than injection of an individual peptide alone. However, injection of GBP together with SRP did not elevate SRP expression at all, indicating the effect of negative feedback regulation. Furthermore, SRP RNAi larvae showed higher body weights compared to controls, and GBP-induced growth retardation was partially abrogated in SRP RNAi larvae. These results led us to conclude that GBP is an upstream cytokine in the regulation of SRP expression and that these cytokines synergistically retard larval growth by repressing feeding activities when insects are exposed to stress conditions.
生长阻断肽(GBP)和应激响应肽(SRP)是昆虫细胞因子,其表达水平可被寄生和高低温等各种应激条件上调。GBP 和 SRP 均作为前体合成并释放到血淋巴中,在血淋巴中被酶切加工为活性肽。将活性 GBP 或 SRP 注射到早期末龄幼虫中,会导致取食减少,进而导致粘虫 Mythimna separata 生长迟缓。虽然这些功能被认为通过影响昆虫的生理和行为而有益于处于应激条件下的昆虫,但 GBP 和 SRP 之间的关系仍不清楚。在这里,我们表明,热应激诱导的活性氧(ROS)升高了血淋巴中的 GBP,从而激活了 SRP 转录并增加了血淋巴中的 SRP 浓度。注射 GBP 和 SRP 均可提高血淋巴中的抗氧化水平。我们发现,在热应激或 HO 注射后 2 至 3 小时,幼虫血淋巴中同时增加了两种活性细胞因子,表明这两种因子具有协同作用。这一推测通过证明同时注射 GBP 和 SRP 比单独注射一种肽引起的食欲下降和生长迟缓更为严重得到了证实。然而,注射 GBP 与 SRP 一起根本不会增加 SRP 的表达,表明存在负反馈调节作用。此外,与对照相比,SRP RNAi 幼虫的体重更高,并且 GBP 诱导的生长迟缓在 SRP RNAi 幼虫中部分被消除。这些结果使我们得出结论,GBP 是调节 SRP 表达的上游细胞因子,并且这些细胞因子通过抑制取食活动协同延缓昆虫暴露于应激条件下的幼虫生长。