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1,25-二羟维生素 D 通过抑制 IPEC-J2 猪肠上皮细胞中的 NF-κB 和 JAK/STAT 信号通路负调控猪流行性腹泻病毒感染的炎症反应。

1,25-Dihydroxyvitamin D 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.

机构信息

Key Laboratory of Animal Disease Resistance and Nutrition, Institute of Animal Nutrition, Sichuan Agricultural University, Chengdu 611130, China.

出版信息

Int J Mol Sci. 2022 Sep 13;23(18):10603. doi: 10.3390/ijms231810603.

Abstract

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 D (1,25(OH)D) has potent anti-inflammatory activity, but it is unknown whether 1,25(OH)D 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)D on PEDV infection in IPEC-J2 cells. The results showed that interleukin 19 () and C-C motif chemokine ligand 20 () gene expression were enhanced with the increase in PEDV infection time in IPEC-J2 cells. Interestingly, 1,25(OH)D supplementation obviously inhibited and expression induced by PEDV. Meanwhile, we also found that 1,25(OH)D reduced -NF-κB, -STAT1, and -STAT3 protein levels induced by PEDV at 24 h post-infection. IκBα and SOCS3, NF-κB, and STAT inhibitor respectively, were increased by 1,25(OH)D supplementation upon PEDV infection. In addition, 1,25(OH)D supplementation inhibited and expression induced by PEDV. Although 1,25(OH)D suppressed the JAK/STAT signal pathway and antiviral gene expression, it had no significant effects on PEDV replication and IFN-α-induced antiviral effects. In addition, when the vitamin D receptor (VDR) was silenced by siRNA, the anti-inflammatory effect of 1,25(OH)D was inhibited. Meanwhile, the overexpression of VDR significantly downregulated and expression induced by PEDV infection. Together, our results provide powerful evidence that 1,25(OH)D could alleviate PEDV-induced inflammation by regulating the NF-κB 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.

摘要

猪流行性腹泻病毒(PEDV)感染可引起仔猪水样腹泻和呕吐。PEDV 感染的发病机制与肠道炎症有关。已知 1,25-二羟维生素 D(1,25(OH)D)具有很强的抗炎活性,但尚不清楚 1,25(OH)D 是否可以抑制 PEDV 诱导的炎症反应及其潜在机制。我们使用转录组分析、基因和蛋白表达、RNA 干扰和过表达等技术研究了 1,25(OH)D 对 IPEC-J2 细胞中 PEDV 感染的抗炎作用。结果表明,随着 PEDV 感染 IPEC-J2 细胞时间的增加,白细胞介素 19()和 C-C 基序趋化因子配体 20()基因表达增强。有趣的是,1,25(OH)D 补充明显抑制了 PEDV 诱导的和表达。同时,我们还发现,1,25(OH)D 降低了 PEDV 感染后 24 小时诱导的-NF-κB、-STAT1 和 -STAT3 蛋白水平。1,25(OH)D 补充物可增加 IκBα 和 SOCS3,它们分别是 NF-κB 和 STAT 的抑制剂,当 PEDV 感染时。此外,1,25(OH)D 补充物抑制了 PEDV 诱导的和表达。尽管 1,25(OH)D 抑制了 JAK/STAT 信号通路和抗病毒基因表达,但对 PEDV 复制和 IFN-α 诱导的抗病毒作用没有显著影响。此外,当维生素 D 受体(VDR)被 siRNA 沉默时,1,25(OH)D 的抗炎作用受到抑制。同时,VDR 的过表达可显著下调 PEDV 感染诱导的和表达。综上所述,我们的研究结果提供了有力的证据,表明 1,25(OH)D 可以通过 VDR 调节 NF-κB 和 JAK/STAT 信号通路来减轻 PEDV 诱导的炎症。这些结果表明,维生素 D 可能有助于抑制 PEDV 感染仔猪的肠道炎症和减轻肠道损伤,为开发预防仔猪 PEDV 感染的营养策略提供了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5474/9504568/e719eb97cbc4/ijms-23-10603-g001.jpg

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