Kim Sung Hwan, Jeung Woonhee, Choi Il-Dong, Jeong Ji-Woong, Lee Dong Eun, Huh Chul-Sung, Kim Geun-Bae, Hong Seong Soo, Shim Jae-Jung, Lee Jung Lyoul, Sim Jae-Hun, Ahn Young-Tae
R&BD Center, Korea Yakult Co. Ltd., Yongin 17086, Republic of Korea.
College of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Republic of Korea.
J Microbiol Biotechnol. 2016 Jun 28;26(6):1035-45. doi: 10.4014/jmb.1512.12002.
To evaluate the effects of lactic acid bacteria (LAB) on Peyer's patch cells, mice were treated with a high dose of kanamycin to disturb the gut microbial environment. The overarching goal was to explore the potential of LAB for use as a dietary probiotic that buffers the negative consequences of antibiotic treatment. In vitro, LAB stimulated the production of immunoglobulin A (IgA) from isolated Peyer's patch cells. Inflammation-related genes (TNF-α, IL-1β, and IL-8) were up-regulated in Caco-2 cells stimulated with lipopolysaccharide (LPS), while tight-junction-related genes (ZO-1 and occludin) were down-regulated; the effects of LPS on inflammatory gene and tight-junction gene expression were reversed by treatment with LAB. Mice treated with a high dose of kanamycin showed increased serum IgE levels and decreases in serum IgA and fecal IgA levels; the number of Peyer's patch cells decreased with kanamycin treatment. However, subsequent LAB treatment was effective in reducing the serum IgE level and recovering the serum IgA and fecal IgA levels, as well as the number of Peyer's patch cells. In addition, ZO-1 and occludin mRNA levels were up-regulated in the ileum tissues of mice receiving LAB treatment. Lactic acid bacteria can enhance the intestinal immune system by improving the integrity of the intestinal barrier and increasing the production of IgA in Peyer's patches. Lactic acid bacteria should be considered a potential probiotic candidate for improving intestinal immunity, particularly in mitigating the negative consequences of antibiotic use.
为了评估乳酸菌(LAB)对派尔集合淋巴结细胞的影响,用高剂量卡那霉素处理小鼠以扰乱肠道微生物环境。总体目标是探索LAB作为膳食益生菌的潜力,以缓冲抗生素治疗的负面影响。在体外,LAB刺激分离的派尔集合淋巴结细胞产生免疫球蛋白A(IgA)。在用脂多糖(LPS)刺激的Caco-2细胞中,炎症相关基因(TNF-α、IL-1β和IL-8)上调,而紧密连接相关基因(ZO-1和闭合蛋白)下调;LAB处理可逆转LPS对炎症基因和紧密连接基因表达的影响。用高剂量卡那霉素处理的小鼠血清IgE水平升高,血清IgA和粪便IgA水平降低;卡那霉素处理使派尔集合淋巴结细胞数量减少。然而,随后的LAB处理有效地降低了血清IgE水平,恢复了血清IgA和粪便IgA水平以及派尔集合淋巴结细胞数量。此外,接受LAB处理的小鼠回肠组织中ZO-1和闭合蛋白mRNA水平上调。乳酸菌可通过改善肠道屏障完整性和增加派尔集合淋巴结中IgA的产生来增强肠道免疫系统。乳酸菌应被视为改善肠道免疫力的潜在益生菌候选物,特别是在减轻抗生素使用的负面影响方面。