# PCV2 Induced Endothelial Derived IL-8 Affects MoDCs Maturation Mainly via NF-κB Signaling Pathway

**Authors:** Mengyu Zhang, Weicheng Xu, Ning Yang, Zhuowei Li, Shuanghai Zhou, Xuewei Liu, Jianfang Wang, Huanrong Li

PMC · DOI: 10.3390/v16040646 · Viruses · 2024-04-22

## TL;DR

This study shows that PCV2 infection in pigs leads to increased IL-8 from endothelial cells, which mainly blocks dendritic cell maturation through the NF-κB signaling pathway.

## Contribution

The study identifies the NF-κB signaling pathway as the main route through which PCV2-induced IL-8 inhibits MoDC maturation.

## Key findings

- PCV2-induced endothelial IL-8 inhibits MoDC maturation primarily via the NF-κB signaling pathway.
- NF-κB p65 nuclear translocation is inhibited in MoDCs exposed to PCV2-induced IL-8.
- Inhibition of the NF-κB pathway reduces IL-12 and GM-CSF mRNA expression in MoDCs.

## Abstract

Porcine circovirus type 2 (PCV2) infection can cause immunosuppressive diseases in pigs. Vascular endothelial cells (VECs), as the target cells for PCV2, play an important role in the immune response and inflammatory regulation. Endothelial IL-8, which is produced by porcine hip artery endothelial cells (PIECs) infected with PCV2, can inhibit the maturation of monocyte-derived dendritic cells (MoDCs). Here, we established a co-culture system of MoDCs and different groups of PIECs to further investigate the PCV2-induced endothelial IL-8 signaling pathway that drives the inhibition of MoDC maturation. The differentially expressed genes related to MoDC maturation were mainly enriched in the NF-κB and JAK2-STAT3 signaling pathways. Both the NF-κB related factor RELA and JAK2-STAT3 signaling pathway related factors (IL2RA, JAK, STAT2, STAT5, IL23A, IL7, etc.) decreased significantly in the IL-8 up-regulated group, and increased significantly in the down-regulated group. The expression of NF-κB p65 in the IL-8 up-regulated group was reduced significantly, and the expression of IκBα was increased significantly. Nuclear translocation of NF-κB p65 was inhibited, while the nuclear translocation of p-STAT3 was increased in MoDCs in the PCV2-induced endothelial IL-8 group. The results of treatment with NF-κB signaling pathway inhibitors showed that the maturation of MoDCs was inhibited and the expression of IL-12 and GM-CSF at mRNA level were lower. Inhibition of the JAK2-STAT3 signaling pathway had no significant effect on maturation, and the expression of IL-12 and GM-CSF at mRNA level produced no significant change. In summary, the NF-κB signaling pathway is the main signaling pathway of MoDC maturation, and is inhibited by the PCV2-induced up-regulation of endothelial-derived IL-8.

## Linked entities

- **Genes:** RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970], IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559], jak (Janus kinase) [NCBI Gene 778659], STAT2 (signal transducer and activator of transcription 2) [NCBI Gene 6773], STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776], IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561], IL7 (interleukin 7) [NCBI Gene 3574], NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792]
- **Proteins:** CXCL8 (C-X-C motif chemokine ligand 8), NFKB1 (nuclear factor kappa B subunit 1), IL12 (Interleukin 12 level), CSF2 (colony stimulating factor 2)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792] {aka EDAID2, IKBA, MAD-3, NFKBI}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL7 (interleukin 7) [NCBI Gene 397253] {aka IL-7}, STAT2 (signal transducer and activator of transcription 2) [NCBI Gene 6773] {aka IMD44, ISGF-3, P113, PTORCH3, STAT113}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CSF2 (colony stimulating factor 2) [NCBI Gene 397208] {aka GM-CSF}, STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776] {aka MGF, STAT5}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}
- **Diseases:** immunosuppressive diseases (MESH:D004194), inflammatory (MESH:D007249), PCV2) infection (MESH:D018173)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11053600/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC11053600/full.md

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Source: https://tomesphere.com/paper/PMC11053600