枯草芽孢杆菌胞外多糖对葡聚糖硫酸钠诱导的结肠炎的保护作用通过维持肠道屏障和抑制炎症反应。

Protective effect of exopolysaccharide fraction from Bacillus subtilis against dextran sulfate sodium-induced colitis through maintenance of intestinal barrier and suppression of inflammatory responses.

机构信息

Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, 26 Kyungheedae-ro, Seoul 02447, Republic of Korea.

Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, 26 Kyungheedae-ro, Seoul 02447, Republic of Korea; Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University, 26 Kyungheedae-ro, Seoul 02447, Republic of Korea.

出版信息

Int J Biol Macromol. 2021 May 1;178:363-372. doi: 10.1016/j.ijbiomac.2021.02.186. Epub 2021 Feb 27.

Abstract

We previously reported that an exopolysaccharide-enriched fraction from Bacillus subtilis J92 (B-EPS) could improve immune functions by regulating the immunological parameters of IFN-γ-primed macrophages, CD3/CD28-stimulated splenocytes, and in cyclophosphamide-induced immunosuppressed mice. In the present study, we investigated whether B-EPS contributes to the maintenance of intestinal barrier integrity in a dextran sodium sulfate (DSS)-induced colitis mouse model that mimics human inflammatory bowel disease (IBD). B-EPS treatment improved histological characteristics and common features including a high disease activity index (DAI), an increased spleen weight, and colon shortening in DSS-induced colitis. B-EPS also effectively restored intestinal barrier function by modulating tight junction-related proteins (claudin-1, claudin-2, and occludin) and epithelial-mesenchymal transition (EMT) marker proteins (E-cadherin, N-cadherin, and vimentin). Moreover, B-EPS downregulated immune cell infiltration and inflammatory responses including the production of inflammatory cytokines, such as IL-6 and IL-1β, and activation of nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 3 (STAT3). Taken together, these results suggest that B-EPS could serve as a functional food ingredient for improving intestinal barrier function and alleviating colonic inflammation in IBD.

摘要

我们之前曾报道过,枯草芽孢杆菌 J92 的富含胞外多糖的部分(B-EPS)可以通过调节 IFN-γ 诱导的巨噬细胞、CD3/CD28 刺激的脾细胞以及环磷酰胺诱导的免疫抑制小鼠的免疫参数来改善免疫功能。在本研究中,我们研究了 B-EPS 是否有助于维持葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠模型中的肠道屏障完整性,该模型模拟了人类炎症性肠病(IBD)。B-EPS 治疗改善了组织学特征和常见特征,包括高疾病活动指数(DAI)、脾重增加和 DSS 诱导的结肠炎中的结肠缩短。B-EPS 还通过调节紧密连接相关蛋白(Claudin-1、Claudin-2 和 Occludin)和上皮-间充质转化(EMT)标记蛋白(E-钙粘蛋白、N-钙粘蛋白和波形蛋白)有效恢复了肠道屏障功能。此外,B-EPS 下调了免疫细胞浸润和炎症反应,包括炎症细胞因子(如 IL-6 和 IL-1β)的产生,以及核因子-kappa B(NF-κB)和信号转导和转录激活因子 3(STAT3)的激活。综上所述,这些结果表明,B-EPS 可以作为一种功能性食品成分,用于改善 IBD 中的肠道屏障功能和缓解结肠炎症。

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