Song Shuo, Zhang Hanqing, Liu Le, Li Minyao, Wang Xiangyu, Zeng Haotao, Zhao Miao, Ran Pixin, Shu Qing, Yang Pingchang
Department of General Practice Medicine, Third Affiliated Hospital, Shenzhen University and State Key Laboratory of Respiratory Diseases Allergy Division at Shenzhen University, Shenzhen, China.
Institute of Allergy & Immunology of Shenzhen University School of Medicine, Shenzhen, China.
Apoptosis. 2025 Feb;30(1-2):239-249. doi: 10.1007/s10495-024-02043-3. Epub 2024 Dec 4.
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.
Th2细胞极化是许多免疫疾病的一个特征;其发病机制仍在阐明之中。益生菌具有免疫调节作用。本研究旨在测试鼠李糖乳杆菌(LR)DNA对调节Th2细胞极化的影响并阐明其潜在机制。在本研究中,采用卵清蛋白加明矾方案在小鼠肠道中建立Th2细胞极化状态。小鼠连续五天每天接受LR-DNA灌胃。使用逆转录定量聚合酶链反应、酶联免疫吸附测定和免疫组织化学评估肠道上皮细胞中程序性细胞死亡配体-1(PD-L1)的表达。结果显示,在小鼠肠道上皮细胞中检测到PD-L1的表达,连续5天每天进行LR-DNA灌胃可使其上调。在T84细胞中也检测到PD-L1的表达,将其置于培养环境中并暴露于LR-DNA可使其增加。RNA测序结果表明,在小鼠肠道上皮细胞中,LR-DNA可上调Kdm5a、foxo1和Pdl1的基因活性。上皮细胞来源的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。给予LR-DNA而非活的益生菌可减轻食物过敏小鼠模型中的实验性Th2细胞极化。总之,LR-DNA诱导肠道上皮细胞产生PD-L1,进而诱导活化的Th2细胞凋亡。给予LR-DNA可减轻肠道中的实验性Th2细胞极化。