1,25-Dihydroxyvitamin D3 Negatively Regulates the Inflammatory Response to Porcine Epidemic Diarrhea Virus Infection by Inhibiting NF-κB and JAK/STAT Signaling Pathway in IPEC-J2 Porcine Epithelial Cells

被引:8
作者
Yang, Jiwen [1 ]
Chen, Daiwen [1 ]
Tian, Gang [1 ]
Mao, Xiangbing [1 ]
He, Jun [1 ]
Zheng, Ping [1 ]
Yu, Jie [1 ]
Luo, Yuheng [1 ]
Luo, Junqiu [1 ]
Huang, Zhiqing [1 ]
Wu, Aimin [1 ]
Yan, Hui [1 ]
Yu, Bing [1 ]
机构
[1] Sichuan Agr Univ, Inst Anim Nutr, Key Lab Anim Dis Resistance & Nutr, Chengdu 611130, Peoples R China
基金
中国国家自然科学基金;
关键词
1,25(OH)(2)D-3; inflammation; PEDV; JAK/STAT signaling pathway; NF-kappa B; HEPATITIS-C VIRUS; VITAMIN-D; ISOLATE US/IOWA/18984/2013; CYTOKINE; ACTIVATION; EXPRESSION; APOPTOSIS; KINASES; PIGLETS; ALPHA;
D O I
10.3390/ijms231810603
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porcine epidemic diarrhea virus (PEDV) infection causes watery diarrhea and vomiting in piglets. The pathogenesis of PEDV infection is related to intestinal inflammation. It is known that 1,25-dihydroxyvitamin D3 (1,25(OH)(2)D-3) has potent anti-inflammatory activity, but it is unknown whether 1,25(OH)(2)D-3 can inhibit the PEDV-induced inflammatory response and the underlying mechanism. We used transcriptome analysis, gene and protein expression, RNA interference and overexpression, and other techniques to study the anti-inflammatory effects of 1,25(OH)(2)D-3 on PEDV infection in IPEC-J2 cells. The results showed that interleukin 19 (IL-19) and C-C motif chemokine ligand 20 (CCL20) gene expression were enhanced with the increase in PEDV infection time in IPEC-J2 cells. Interestingly, 1,25(OH)(2)D-3 supplementation obviously inhibited IL-19 and CCL20 expression induced by PEDV. Meanwhile, we also found that 1,25(OH)(2)D-3 reduced p-NF-kappa B, p-STAT1, and p-STAT3 protein levels induced by PEDV at 24 h post-infection. I kappa B alpha and SOCS3, NF-kappa B, and STAT inhibitor respectively, were increased by 1,25(OH)(2)D-3 supplementation upon PEDV infection. In addition, 1,25(OH)(2)D-3 supplementation inhibited ISG15 and MxA expression induced by PEDV. Although 1,25(OH)(2)D-3 suppressed the JAK/STAT signal pathway and antiviral gene expression, it had no significant effects on PEDV replication and IFN-alpha-induced antiviral effects. In addition, when the vitamin D receptor (VDR) was silenced by siRNA, the anti-inflammatory effect of 1,25(OH)(2)D-3 was inhibited. Meanwhile, the overexpression of VDR significantly downregulated IL-19 and CCL20 expression induced by PEDV infection. Together, our results provide powerful evidence that 1,25(OH)(2)D-3 could alleviate PEDV-induced inflammation by regulating the NF-kappa B and JAK/STAT signaling pathways through VDR. These results suggest that vitamin D could contribute to inhibiting intestinal inflammation and alleviating intestinal damage in PEDV-infected piglets, which offers new approaches for the development of nutritional strategies to prevent PEDV infection in piglets.
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页数:16
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