Zhu Xinting, Liu Fang, Wu Qinyi, Li Sanhua, Ruan Guoyong, Yang Jianbo, Yu Changyan, Jiang Nian, Xiao Yi, Liu Yun
Guizhou Provincial College-based Key Lab for Tumor Prevention and Treatment with Distinctive Medicines, Zunyi Medical University, Zunyi, Guizhou 563000, China; College of Basic Medicine, Zunyi Medical University, Zunyi, Guizhou 563000, China.
Yunnan Provincial Key Laboratory of Molecular Biology for Sinomedicine, Yunnan University of Chinese Medicine, Kunming, Yunnan 650000, China.
Int Immunopharmacol. 2022 Dec;113(Pt A):109385. doi: 10.1016/j.intimp.2022.109385. Epub 2022 Oct 30.
The conserved p38/PMK-1 pathway that is an evolutionarily conserved module used by mammals and nematodes in immune response against bacterial infections. Brevilin A (BA), a sesquiterpene lactone compound of Centipeda minima has been shown to exhibit activities such as anti-tumor, anti-bacterial and anti-protozoal. However, whether the Brevilin A influences the immune response and the underlying molecular mechanisms remain obscure. We find that 10 μM Brevilin A increases resistance to not only the Gram-negative pathogens Pseudomonas aeruginosa and Salmonella enterica but also the Gram-positive pathogens Enterococcusfaecalis and Staphylococcus aureus. Meanwhile, Brevilin A enhances the resistance to pathogens by reducing the bacterial burden in the intestine. Through the genetic screening in C. elegans, we find that Brevilin A promotes innate immunity via p38 MAPK pathway. Furthermore, Brevilin A activates the p38/PMK-1 in the intestine for innate immune response. In addition, we also find that Brevilin A increases the resistance of oxidative stress and extends lifespan through p38 MAPK pathway. Our work suggests that Brevilin A may be a viable candidate for the treatment of infectious diseases.
保守的p38/PMK-1信号通路是哺乳动物和线虫在针对细菌感染的免疫反应中使用的一种进化上保守的模块。短叶老鹳草素A(BA)是鹅不食草的一种倍半萜内酯化合物,已被证明具有抗肿瘤、抗菌和抗原虫等活性。然而,短叶老鹳草素A是否影响免疫反应及其潜在的分子机制仍不清楚。我们发现,10μM的短叶老鹳草素A不仅能增强对革兰氏阴性病原体铜绿假单胞菌和肠炎沙门氏菌的抵抗力,还能增强对革兰氏阳性病原体粪肠球菌和金黄色葡萄球菌的抵抗力。同时,短叶老鹳草素A通过减少肠道内的细菌负荷来增强对病原体的抵抗力。通过在秀丽隐杆线虫中的基因筛选,我们发现短叶老鹳草素A通过p38丝裂原活化蛋白激酶(MAPK)信号通路促进先天免疫。此外,短叶老鹳草素A激活肠道中的p38/PMK-1以引发先天免疫反应。此外,我们还发现短叶老鹳草素A通过p38 MAPK信号通路增加氧化应激抵抗力并延长寿命。我们的研究表明,短叶老鹳草素A可能是治疗传染病的一个可行候选药物。