鼠李糖乳酪杆菌B6胞外多糖对脂多糖诱导Caco-2细胞损伤的影响OA
Effects of Lacticaseibacillus rhamnosus B6 exopolysaccharides on lipopolysaccharide-induced damage in Caco-2 cells
为探索乳杆菌产生胞外多糖(exopolysaccharides,EPS)对脂多糖(lipopolysaccharide,LPS)引起的肠屏障损伤的保护作用及相关机制,该研究以前期从鼠李糖乳酪杆菌B6(Lacticaseibacillus rhamnosus B6)代谢产物中分离纯化得到的纯组分、结构明确的多糖(B6-EPS)为对象,从细胞活力、炎性因子水平、Caco-2细胞单层电阻及通透性、紧密连接蛋白表达等方面,综合探讨B6-EPS体外对LPS诱导Caco-2细胞损伤的改善效果.结果显示,以200 μg/mL的B6-EPS干预可以显著提升Caco-2细胞的活力(P<0.05),提升抑炎因子IL-10的水平(P<0.01),并通过促进紧密连接蛋白CLDN3的表达,提升Caco-2细胞单层的致密性,从而缓解脂多糖引起的Caco-2细胞损伤.此外,基因差异分析结果也为B6-EPS调节细胞炎症及氧化应激方面提供潜在新靶点.整体而言,该研究结果为益生菌胞外多糖保护脂多糖诱导肠屏障损伤作用提供科学支持,为后续以CLDN3为靶点调控肠屏障功能的深层机制探索提供依据.
To explore the protective effects and underlying mechanisms of Lactobacillus exopolysaccharides against lipopolysaccharide-induced intestinal barrier damage,a pure and structurally well-characterized polysaccharide(B6-EPS)isolated and purified from Lactica-seibacillus rhamnosus B6 was used as the research subject.The improvement effect of B6-EPS on LPS-induced injury in Caco-2 cell was systematically evaluated from multiple perspectives in vitro,including cell viability,inflammatory factor levels,transepithelial electrical resistance and permeability of Caco-2 cell monolayers,and tight junction protein expression.The results demonstrated that intervention with 200 μg/mL B6-EPS could significantly improve the viability of Caco-2 cells(P<0.05),enhance the level of anti-inflammatory fac-tor IL-10(P<0.01),and promote the expression of tight junction protein CLDN3 to improve the integrity of Caco-2 cell monolayers,thereby alleviating LPS-induced Caco-2 cell injury.In addition,the results of gene differential analysis also provided potential new targets for B6-EPS in regulating cellular inflammation and oxidative stress.Overall,the findings of this study provide scientific support for the pro-tective effect of probiotic exopolysaccharides against lipopolysaccharide-induced intestinal barrier damage,and lay a foundation for further investigations into the deep mechanisms by which CLDN3 mediates the regulation of intestinal barrier function.
王丹其;胡丹;韩瑨
光明乳业股份有限公司乳业研究院,上海乳业生物工程技术研究中心,乳业生物技术国家重点实验室,上海,200436光明乳业股份有限公司乳业研究院,上海乳业生物工程技术研究中心,乳业生物技术国家重点实验室,上海,200436光明乳业股份有限公司乳业研究院,上海乳业生物工程技术研究中心,乳业生物技术国家重点实验室,上海,200436
鼠李糖乳酪杆菌胞外多糖肠道屏障紧密连接蛋白
Lacticaseibacillus rhamnosusexopolysaccharidesintestinal barriertight junction proteins
《食品与发酵工业》 2026 (10)
51-58,8
十四五国家重点研发计划(2022YFD2100704)上海市自然科学基金项目(23ZR1414400)
评论