College of Animal Science & Technology, Shihezi University, Shihezi, Xinjiang, 832003, China.
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu, 730046, China.
Korean J Parasitol. 2022 Apr;60(2):117-126. doi: 10.3347/kjp.2022.60.2.117. Epub 2022 Apr 20.
Cystatin, a cysteine protease inhibitor found in many parasites, plays important roles in immune evasion. This study analyzed the molecular characteristics of a cystatin from Fasciola hepatica (FhCystatin) and expressed recombinant FhCystatin (rFhcystatin) to investigate the immune modulatory effects on lipopolysaccharide-induced proliferation, migration, cytokine secretion, nitric oxide (NO) production, and apoptosis in mouse macrophages. The FhCystatin gene encoded 116 amino acids and contained a conserved cystatin-like domain. rFhCystatin significantly inhibited the activity of cathepsin B. rFhCystatin bound to the surface of mouse RAW264.7 cells, significantly inhibited cell proliferation and promoted apoptosis. Moreover, rFhCystatin inhibited the expression of cellular nitric oxide, interleukin-6, and tumor necrosis factor-α, and promoted the expression of transforming growth factor-β and interleukin-10. These results showed that FhCystatin played an important role in regulating the activity of mouse macrophages. Our findings provide new insights into mechanisms underlying the immune evasion and contribute to the exploration of potential targets for the development of new drug to control F. hepatica infection.
半胱氨酸蛋白酶抑制剂(cystatin)是一种存在于许多寄生虫中的半胱氨酸蛋白酶抑制剂,在免疫逃避中发挥着重要作用。本研究分析了肝片形吸虫(Fasciola hepatica)半胱氨酸蛋白酶抑制剂(FhCystatin)的分子特征,并表达了重组 FhCystatin(rFhcystatin),以研究其对脂多糖诱导的小鼠巨噬细胞增殖、迁移、细胞因子分泌、一氧化氮(NO)产生和凋亡的免疫调节作用。FhCystatin 基因编码 116 个氨基酸,含有保守的半胱氨酸蛋白酶抑制剂样结构域。rFhCystatin 显著抑制组织蛋白酶 B 的活性。rFhCystatin 与小鼠 RAW264.7 细胞表面结合,显著抑制细胞增殖并促进细胞凋亡。此外,rFhCystatin 抑制细胞内一氧化氮、白细胞介素-6 和肿瘤坏死因子-α的表达,并促进转化生长因子-β和白细胞介素-10 的表达。这些结果表明,FhCystatin 在调节小鼠巨噬细胞活性方面发挥着重要作用。我们的研究结果为免疫逃避的机制提供了新的见解,并为探索控制肝片形吸虫感染的新药物靶点提供了依据。