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膳食纤维鼠李半乳糖醛酸聚糖以一种不依赖于微生物群的方式改善肠道上皮屏障功能。

The dietary fibre rhamnogalacturonan improves intestinal epithelial barrier function in a microbiota-independent manner.

机构信息

Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta, Canada.

Department of Biochemistry, Universidade Federal do Acre, Rio Branco, Brazil.

出版信息

Br J Pharmacol. 2022 Jan;179(2):337-352. doi: 10.1111/bph.15739. Epub 2021 Dec 22.

Abstract

BACKGROUND AND PURPOSE

Dietary fibre comprises a complex group of polysaccharides that are indigestible but are fermented by gut microbiota, promoting beneficial effects to the intestinal mucosa indirectly through the production of short chain fatty acids. We found that a polysaccharide, rhamnogalacturonan (RGal), from the plant Acmella oleracea, has direct effects on intestinal epithelial barrier function. Our objective was to determine the mechanism whereby RGal enhances epithelial barrier function.

EXPERIMENTAL APPROACH

Monolayers of colonic epithelial cell lines (Caco-2, T84) and of human primary cells from organoids were mounted in Ussing chambers to assess barrier function. The cellular mechanism of RGal effects on barrier function was determined using inhibitors of TLR-4 and PKC isoforms.

KEY RESULTS

Apically applied RGal (1000 μg ml ) significantly enhanced barrier function as shown by increased transepithelial electrical resistance (TER) and reduced fluorescein isothiocyanate (FITC)-dextran flux in Caco-2, T84 and human primary cell monolayers, and accelerated tight junction reassembly in Caco-2 cells in a calcium switch assay. RGal also reversed the barrier-damaging effects of inflammatory cytokines on FITC-dextran flux and preserved the tight junction distribution of occludin. RGal activated TLR4 in TLR4-expressing HEK reporter cells, an effect that was inhibited by the TLR4 inhibitor, C34. The effect of RGal was also dependent on PKC, specifically the isoforms PKCδ and PKCζ.

CONCLUSION AND IMPLICATIONS

RGal enhances intestinal epithelial barrier function through activation of TLR4 and PKC signalling pathways. Elucidation of RGal mechanisms of action could lead to new, dietary approaches to enhance mucosal healing in inflammatory bowel diseases.

摘要

背景与目的

膳食纤维由一组复杂的多糖组成,这些多糖不能被消化,但可被肠道微生物群发酵,通过产生短链脂肪酸间接促进肠黏膜有益作用。我们发现,来自植物 Acmella oleracea 的多糖鼠李半乳糖醛酸聚糖(RGal)对肠上皮屏障功能具有直接作用。我们的目的是确定 RGal 增强上皮屏障功能的机制。

实验方法

将结肠上皮细胞系(Caco-2、T84)和类器官来源的人原代细胞的单层置于 Ussing 室中,以评估屏障功能。使用 TLR-4 和 PKC 同工型抑制剂来确定 RGal 对屏障功能的影响的细胞机制。

主要结果

RGal(1000μg/ml)在上皮细胞单层中呈浓度依赖性增加紧密连接的再组装,在 Caco-2 细胞中的钙转换测定中,RGal 显著增强了屏障功能,表现为跨上皮电阻(TER)增加,荧光素异硫氰酸酯(FITC)-葡聚糖通量减少。RGal 还逆转了炎症细胞因子对 FITC-葡聚糖通量的屏障破坏作用,并保留了 occludin 的紧密连接分布。RGal 在表达 TLR4 的 HEK 报告细胞中激活 TLR4,该作用可被 TLR4 抑制剂 C34 抑制。RGal 的作用还依赖于 PKC,特别是 PKCδ 和 PKCζ 同工型。

结论和意义

RGal 通过激活 TLR4 和 PKC 信号通路增强肠道上皮屏障功能。阐明 RGal 的作用机制可能会导致新的饮食方法来增强炎症性肠病中的黏膜愈合。

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