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通过改变肠道微生物群和调节树突状细胞激活来减轻小鼠的肠道炎症。

Alleviates Intestinal Inflammation in Mice by Altering Gut Microbiota and Regulating Dendritic Cell Activation via CD83.

机构信息

Department of Biomedical Science, Ajou University School of Medicine, Suwon 16499, Korea.

Department of Microbiology, Ajou University School of Medicine, Suwon 16499, Korea.

出版信息

Cells. 2022 Jun 12;11(12):1903. doi: 10.3390/cells11121903.

Abstract

Ulcerative colitis (UC) is one of the major subtypes of inflammatory bowel disease with unknown etiology. Probiotics have recently been introduced as a treatment for UC. () is a lactic acid-producing bacterium that survives in environments with high salt concentrations, though little is known about its immunomodulatory function as a probiotic. The purpose of this study is to determine whether exerts an anti-inflammatory effect on intestinal inflammation in mice. Colitis was induced in C57BL/6J mice by feeding 4% DSS in drinking water for 7 days. was orally administered with DSS. Anti-inflammatory functions were subsequently evaluated by flow cytometry, qRT-PCT, and ELISA. Gut microbial composition was analyzed by 16S rRNA metagenomic analysis. DSS-induced colitis mice treated with showed less weight loss and significantly suppressed colonic shortening compared to DSS-induced colitis mice. significantly reduced the frequency of the dendritic cell activation molecule CD83 in peripheral blood leukocytes and intestinal epithelial lymphocytes. Frequencies of CD8+NK1.1+ cells decreased in mice with colitis after treatment and IL-1β levels were also reduced. Alteration of gut microbiota was observed in mice with colitis after administration of . These results suggest is effective in alleviating DSS-induced colitis in mice by altering immune regulation and gut microbiome compositions.

摘要

溃疡性结肠炎(UC)是一种病因不明的炎症性肠病的主要亚型。益生菌最近被引入作为 UC 的治疗方法。() 是一种产乳酸的细菌,能够在高盐浓度的环境中生存,但作为益生菌的免疫调节功能知之甚少。本研究的目的是确定是否对小鼠的肠道炎症具有抗炎作用。通过在饮用水中添加 4% DSS 喂养 7 天,在 C57BL/6J 小鼠中诱导结肠炎。用 DSS 口服给予。随后通过流式细胞术、qRT-PCT 和 ELISA 评估抗炎功能。通过 16S rRNA 宏基因组分析分析肠道微生物组成。与 DSS 诱导的结肠炎小鼠相比,用 处理的 DSS 诱导的结肠炎小鼠体重减轻较少,结肠缩短明显受到抑制。在结肠炎小鼠中,治疗显著降低了外周血白细胞和肠上皮淋巴细胞中树突状细胞激活分子 CD83 的频率。在用 处理后的结肠炎小鼠中,CD8+NK1.1+细胞的频率降低,IL-1β 水平也降低。在给予 后,结肠炎小鼠的肠道微生物群发生了改变。这些结果表明,通过改变免疫调节和肠道微生物组组成,对 DSS 诱导的结肠炎小鼠具有治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50dc/9221263/cada58d58f22/cells-11-01903-g001.jpg

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