Laboratorio de Bacteriologia, Instituto Butantan, São Paulo, Brazil.
Cell Immunol. 2012 Jan-Feb;275(1-2):5-11. doi: 10.1016/j.cellimm.2012.04.003. Epub 2012 Apr 7.
Mygalin is an antibacterial molecule isolated from the hemocytes of the spider Acanthoscurria gomesiana. It was identified as bis-acylpolyamine spermidine. We evaluated the modulator effects of synthetic Mygalin in the innate immune response. We demonstrate that Mygalin induces IFN-γ synthesis by splenocytes increasing the nitrite secretion by splenocytes and macrophages. A specific inhibitor of iNOS abrogated Mygalin-induced nitrite production in macrophages independent of IFN-γ activation. In addition, Mygalin-activated macrophages produced TNF-α but not IL-1β, demonstrating that Mygalin does not act directly on the inflammasome. Furthermore, this compound did not affect spontaneous or Concanavalin A-induced proliferative responses by murine splenocytes and did not induce IL-5 or apoptosis of splenocytes or bone marrow-derived macrophages. These data provide evidence that Mygalin modulates the innate immune response by inducing IFN-γ and NO synthesis. The combined immune regulatory and antibacterial qualities of Mygalin should be explored as a strategy to enhance immune responses in infection.
麦加拉因是从蜘蛛 Acanthoscurria gomesiana 的血细胞中分离出来的一种抗菌分子。它被鉴定为双酰基多胺亚精胺。我们评估了合成麦加拉因在先天免疫反应中的调节剂作用。我们证明麦加拉因通过增加脾细胞和巨噬细胞的亚硝酸盐分泌来诱导 IFN-γ 的合成。iNOS 的特异性抑制剂可消除巨噬细胞中麦加拉因诱导的亚硝酸盐产生,而不依赖 IFN-γ 的激活。此外,麦加拉因激活的巨噬细胞产生 TNF-α,但不产生 IL-1β,表明麦加拉因不会直接作用于炎症小体。此外,该化合物不影响小鼠脾细胞的自发或刀豆蛋白 A 诱导的增殖反应,也不诱导脾细胞或骨髓来源的巨噬细胞中的 IL-5 或凋亡。这些数据表明,麦加拉因通过诱导 IFN-γ 和 NO 合成来调节先天免疫反应。应探索麦加拉因的联合免疫调节和抗菌特性,作为增强感染中免疫反应的一种策略。