Department of Biomolecular Innovation, Institute for Biomedical Sciences, Shinshu University, Nagano, 399-4598, Japan.
Food and Feed Immunology Group, Laboratory of Animal Food Function, Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, 980-8572, Japan.
World J Microbiol Biotechnol. 2024 Oct 24;40(11):363. doi: 10.1007/s11274-024-04157-x.
Interleukin (IL) 36 is a member of the IL-1-like proinflammatory cytokine family that has a protective role in mucosal immunity. We hypothesized that mucosal delivery of IL-36γ to the intestine would be a very effective way to prevent intestinal diseases. Here, we genetically engineered a lactic acid bacterium, Lactococcus lactis, to produce recombinant mouse IL-36γ (rmIL-36γ). Western blotting and enzyme-linked immunosorbent assay results showed that the engineered strain (NZ-IL36γ) produced and hypersecreted the designed rmIL-36γ in the presence of nisin, which induces the expression of the recombinant gene. We administered NZ-IL36γ to mice via oral gavage, and collected the ruminal contents and rectal tissues. Colony PCR using primers specific for NZ-IL36γ, and enzyme-linked immunosorbent assay to measure the rmIL-36γ concentrations of the ruminal contents showed that NZ-IL36γ colonized the mouse intestines and secreted rmIL-36γ. A microbiota analysis revealed increased abundances of bacteria of the genera Acetatifactor, Eubacterium, Monoglobus, and Roseburia in the mouse intestines. Real-time quantitative PCR of the whole colon showed increased Muc2 expression. An in vitro assay using murine colorectal epithelial cells and human colonic cells showed that purified rmIL-36γ promoted Muc2 gene expression. Taken together, these data suggest that NZ-IL36γ may be an effective and attractive tool for delivering rmIL-36γ to improve the intestinal environment.
白细胞介素 (IL) 36 是白细胞介素 1 样前炎性细胞因子家族的一员,在黏膜免疫中具有保护作用。我们假设将 IL-36γ 递送到肠道黏膜将是预防肠道疾病的非常有效方法。在这里,我们通过基因工程将乳酸乳球菌(Lactococcus lactis)改造为生产重组鼠白细胞介素 36γ(rmIL-36γ)。Western blot 和酶联免疫吸附试验结果表明,在乳链菌肽诱导重组基因表达的存在下,工程菌株(NZ-IL36γ)产生并过度分泌设计的 rmIL-36γ。我们通过口服灌胃将 NZ-IL36γ 施用于小鼠,并收集瘤胃液和直肠组织。使用针对 NZ-IL36γ 的引物进行的菌落 PCR,以及酶联免疫吸附试验测量瘤胃液中的 rmIL-36γ 浓度表明,NZ-IL36γ 定植于小鼠肠道并分泌 rmIL-36γ。微生物组分析显示,小鼠肠道中属名 Acetatifactor、Eubacterium、Monoglobus 和 Roseburia 的细菌丰度增加。整个结肠的实时定量 PCR 显示 Muc2 表达增加。使用鼠结直肠上皮细胞和人结肠细胞的体外试验表明,纯化的 rmIL-36γ 促进 Muc2 基因表达。综上所述,这些数据表明 NZ-IL36γ 可能是一种将 rmIL-36γ 递送到改善肠道环境的有效且有吸引力的工具。