Probiotic DNA regulates intestinal Th2 polarization by inducing epithelial cells to produce PD-L1.

IF 6.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shuo Song, Hanqing Zhang, Le Liu, Minyao Li, Xiangyu Wang, Haotao Zeng, Miao Zhao, Pixin Ran, Qing Shu, Pingchang Yang
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Abstract

Th2 polarization is a characteristic feature of many immune diseases; its pathogenesis is still being elucidated. Probiotics have immune regulatory effects. This study is aimed at testing the impact of Lactobacillus rhamnosus (LR) DNA on regulating Th2 polarization and elucidating its underlying mechanism. In this study, ovalbumin plus alum protocol was used to establish the Th2 polarization status in the mouse intestine. Mice received LR-DNA gavage daily for five days. The expression of programmed cell death ligand-1 (PD-L1) in intestinal epithelial cells was assessed using RT-qPCR, enzyme-linked immunosorbent assay, and immunohistochemistry. The results showed that the expression of PD-L1 was detected in mouse intestinal epithelial cells, which was up regulated by LR-DNA gavage daily for 5 days. The expression of PD-L1 was also detected in T84 cells, which could be increased by exposing them to LR-DNA in culture. RNA sequencing results showed that the gene activities of Kdm5a, foxo1 and Pdl1 could be upregulated by LR-DNA in mouse intestinal epithelial cells. The epithelial cell-derived PD-L1 induced the activated Th2 cell apoptosis by interacting with programmed cell death protein-1 (PD-1). Administration of LR-DNA, but not live probiotics, alleviated experimental Th2 polarization in a food allergy mouse model. In conclusion, LR-DNA induces intestinal epithelial cells to produce PD-L1, which induces the activated Th2 cell apoptosis. Administration of LR-DNA mitigated experimental Th2 polarization in the intestine.

益生菌DNA通过诱导上皮细胞产生PD-L1调节肠道Th2极化。
Th2极化是许多免疫疾病的特征;其发病机制尚不清楚。益生菌具有免疫调节作用。本研究旨在检测鼠李糖乳杆菌(Lactobacillus rhamnosus, LR) DNA对Th2极化的调控作用,并阐明其潜在机制。本研究采用卵清蛋白加明矾方案建立小鼠肠道中Th2极化状态。小鼠每天灌胃LR-DNA,连续5天。采用RT-qPCR、酶联免疫吸附法和免疫组织化学检测肠上皮细胞中程序性细胞死亡配体-1 (PD-L1)的表达。结果表明,小鼠肠上皮细胞中检测到PD-L1的表达,每天灌胃5 d后PD-L1表达上调。在T84细胞中也检测到PD-L1的表达,将其暴露于培养的LR-DNA中可以增加PD-L1的表达。RNA测序结果显示,LR-DNA可上调小鼠肠上皮细胞中Kdm5a、foxo1和Pdl1的基因活性。上皮细胞源性PD-L1通过与程序性细胞死亡蛋白-1 (PD-1)相互作用诱导活化的Th2细胞凋亡。在食物过敏小鼠模型中,给予LR-DNA而非活益生菌可减轻实验性Th2极化。综上所述,LR-DNA诱导肠上皮细胞产生PD-L1, PD-L1诱导活化的Th2细胞凋亡。给药LR-DNA减轻了实验性肠内Th2极化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Apoptosis
Apoptosis 生物-生化与分子生物学
CiteScore
9.10
自引率
4.20%
发文量
85
审稿时长
1 months
期刊介绍: Apoptosis, a monthly international peer-reviewed journal, focuses on the rapid publication of innovative investigations into programmed cell death. The journal aims to stimulate research on the mechanisms and role of apoptosis in various human diseases, such as cancer, autoimmune disease, viral infection, AIDS, cardiovascular disease, neurodegenerative disorders, osteoporosis, and aging. The Editor-In-Chief acknowledges the importance of advancing clinical therapies for apoptosis-related diseases. Apoptosis considers Original Articles, Reviews, Short Communications, Letters to the Editor, and Book Reviews for publication.
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