Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
Lactic Acid Bacteria Laboratory, Department of Biotechnology, Instituto de Agroquimicay Tecnologia de Alimentos, Spanish National Research Council (C.S.I.C.), Valencia, Spain.
Inflamm Bowel Dis. 2020 Jul 17;26(8):1199-1211. doi: 10.1093/ibd/izaa049.
Probiotic lactic acid bacteria (LAB) have been used in the anti-inflammation and anti-infection process of various diseases, including inflammatory bowel disease (IBD). Vitamin D receptor (VDR) plays an essential role in pathogenesis of IBD and infectious diseases. Previous studies have demonstrated that the human VDR gene is a key host factor to shape gut microbiome. Furthermore, intestinal epithelial VDR conditional knockout (VDRΔIEC) leads to dysbiosis. Low expressions of VDR is associated with impaired autophagy, accompanied by a reduction of ATG16L1 and LC3B. The purpose of this study is to investigate probiotic effects and mechanism in modulating the VDR-autophagy pathways.
Five LAB strains were isolated from Korean kimchi. Conditional medium (CM) from these strains was used to treat a human cell line HCT116 or intestinal organoids to measure the expression of VDR and autophagy. Mouse embryonic fibroblast (MEF) cells with or without VDR were used to investigate the dependence on the VDR signaling. To test the role of LAB in anti-inflammation, VDR+/+ organoids were treated with 121-CM before infection with Salmonella enterica serovar Enteritidis. In vivo, the role of LAB in regulating VDR-autophagy signaling was examined using LAB 121-CM orally administrated to VDRLoxp and VDRΔIEC mice.
The LAB-CM-treated groups showed higher mRNA expression of VDR and its target genes cathelicidin compared with the control group. LAB treatment also enhanced expressions of Beclin-1 and ATG16L1 and changed the ratio of LC3B I and II, indicating the activation of autophagic responses. Furthermore, 121-CM treatment before Salmonella enterica serovar Enteritidis infection dramatically increased VDR and ATG16L1 and inhibited the inflammation. Administration of 121-CM to VDRLoxp and VDRΔIEC mice for 12 and 24 hours resulted in an increase of VDR and LC3B II:I ratio. Furthermore, we identified that probiotic proteins P40 and P75 in the LAB-CM contributed to the anti-inflammatory function by increasing VDR.
Probiotic LAB exert anti-inflammation activity and induces autophagy. These effects depend on the VDR expression. Our data highlight the beneficial effects of these 5 LAB strains isolated from food in anti-infection and anti-inflammation.
益生菌乳酸菌(LAB)已被用于各种疾病的抗炎和抗感染过程,包括炎症性肠病(IBD)。维生素 D 受体(VDR)在 IBD 和传染病的发病机制中起着至关重要的作用。先前的研究表明,人类 VDR 基因是塑造肠道微生物组的关键宿主因素。此外,肠道上皮细胞 VDR 条件性敲除(VDRΔIEC)会导致菌群失调。VDR 的低表达与自噬受损有关,同时伴随着 ATG16L1 和 LC3B 的减少。本研究的目的是探讨益生菌对调节 VDR-自噬途径的作用及机制。
从韩国泡菜中分离出 5 株 LAB 菌株。使用这些菌株的条件培养基(CM)处理人结肠癌细胞系 HCT116 或肠类器官,以测量 VDR 和自噬的表达。使用有或没有 VDR 的小鼠胚胎成纤维细胞(MEF)细胞来研究对 VDR 信号的依赖性。为了测试 LAB 在抗炎中的作用,在沙门氏菌肠亚种 Enteritidis 感染前用 121-CM 处理 VDR+/+类器官。在体内,通过口服 LAB 121-CM 处理 VDRLoxp 和 VDRΔIEC 小鼠,来研究 LAB 在调节 VDR-自噬信号中的作用。
与对照组相比,LAB-CM 处理组的 VDR 及其靶基因 cathelicidin 的 mRNA 表达更高。LAB 处理还增强了 Beclin-1 和 ATG16L1 的表达,并改变了 LC3B I 和 II 的比值,表明自噬反应的激活。此外,沙门氏菌肠亚种 Enteritidis 感染前用 121-CM 处理可显著增加 VDR 和 ATG16L1,并抑制炎症。用 121-CM 处理 VDRLoxp 和 VDRΔIEC 小鼠 12 和 24 小时后,VDR 和 LC3B II:I 比值增加。此外,我们发现 LAB-CM 中的益生菌蛋白 P40 和 P75 通过增加 VDR 发挥抗炎作用。
益生菌 LAB 发挥抗炎作用并诱导自噬。这些作用取决于 VDR 的表达。我们的数据突出了从食物中分离出的这 5 株 LAB 菌株在抗感染和抗炎方面的有益作用。