Shigemori Suguru, Watanabe Takafumi, Kudoh Kai, Ihara Masaki, Nigar Shireen, Yamamoto Yoshinari, Suda Yoshihito, Sato Takashi, Kitazawa Haruki, Shimosato Takeshi
Department of Bioscience and Food Production Science, Interdisciplinary Graduate School of Science and Technology, Shinshu University, 8304 Minamiminowa, Kamiina, Nagano, 399-4598, Japan.
Research Fellow of the Japan Society for the Promotion of Science, Japan Society for the Promotion of Science (JSPS), 5-3-1, Kojimachi, Chiyoda-ku, Tokyo, 102-0083, Japan.
Microb Cell Fact. 2015 Nov 25;14:189. doi: 10.1186/s12934-015-0378-2.
Mucosal delivery of therapeutic proteins using genetically modified strains of lactic acid bacteria (gmLAB) is being investigated as a new therapeutic strategy.
We developed a strain of gmLAB, Lactococcus lactis NZ9000 (NZ-HO), which secretes the anti-inflammatory molecule recombinant mouse heme oxygenase-1 (rmHO-1). The effects of short-term continuous oral dosing with NZ-HO were evaluated in mice with dextran sulfate sodium (DSS)-induced acute colitis as a model of inflammatory bowel diseases (IBD).
We identified the secretion of rmHO-1 by NZ-HO. rmHO-1 was biologically active as determined with spectroscopy. Viable NZ-HO was directly delivered to the colon via oral administration, and rmHO-1 was secreted onto the colonic mucosa in mice. Acute colitis in mice was induced by free drinking of 3 % DSS in water and was accompanied by an increase in the disease activity index score and histopathological changes. Daily oral administration of NZ-HO significantly improved these colitis-associated symptoms. In addition, NZ-HO significantly increased production of the anti-inflammatory cytokine interleukin (IL)-10 and decreased the expression of pro-inflammatory cytokines such as IL-1α and IL-6 in the colon compared to a vector control strain.
Oral administration of NZ-HO alleviates DSS-induced acute colitis in mice. Our results suggest that NZ-HO may be a useful mucosal therapeutic agent for treating IBD.
利用基因工程改造的乳酸菌(gmLAB)进行治疗性蛋白质的黏膜递送作为一种新的治疗策略正在研究中。
我们构建了一种gmLAB菌株,乳酸乳球菌NZ9000(NZ-HO),其可分泌抗炎分子重组小鼠血红素加氧酶-1(rmHO-1)。以硫酸葡聚糖钠(DSS)诱导的急性结肠炎小鼠作为炎症性肠病(IBD)的模型,评估NZ-HO短期连续口服给药的效果。
我们鉴定出NZ-HO可分泌rmHO-1。通过光谱分析确定rmHO-1具有生物活性。活性NZ-HO通过口服直接递送至结肠,并且rmHO-1在小鼠结肠黏膜上分泌。通过自由饮用含3% DSS的水诱导小鼠急性结肠炎,其伴有疾病活动指数评分增加和组织病理学变化。每日口服NZ-HO可显著改善这些与结肠炎相关的症状。此外,与载体对照菌株相比,NZ-HO显著增加了抗炎细胞因子白细胞介素(IL)-10的产生,并降低了结肠中促炎细胞因子如IL-1α和IL-6的表达。
口服NZ-HO可减轻DSS诱导的小鼠急性结肠炎。我们的结果表明NZ-HO可能是一种治疗IBD的有用的黏膜治疗剂。