NDV-induced autophagy enhances inflammation through NLRP3/Caspase-1 inflammasomes and the p38/MAPK pathway.
Juncheng CaiSiyuan WangHaoyun DuLei FanWeiFeng YuanQiufan XuJinlian RenQiuyan LinBin XiangChan DingTao RenLibin ChenPublished in: Veterinary research (2023)
Newcastle disease (ND), caused by the Newcastle disease virus (NDV), is a highly virulent infectious disease of poultry. Virulent NDV can cause severe autophagy and inflammation in host cells. While studies have shown a mutual regulatory relationship between autophagy and inflammation, this relationship in NDV infection remains unclear. This study confirmed that NDV infection could trigger autophagy in DF-1 cells to promote cytopathic and viral replication. NDV-induced autophagy was positively correlated with the mRNA levels of inflammatory cytokines such as IL-1β, IL-8, IL-18, CCL-5, and TNF-α, suggesting that NDV-induced autophagy promotes the expression of inflammatory cytokines. Further investigation demonstrated that NLRP3 protein expression, Caspase-1 activity, and p38 phosphorylation level positively correlated with autophagy, suggesting that NDV-induced autophagy could promote the expression of inflammatory cytokines through NLRP3/Caspase-1 inflammasomes and p38/MAPK pathway. In addition, NDV infection also triggered mitochondrial damage and mitophagy in DF-1 cells, but did not result in a large leakage of reactive oxygen species (ROS) and mitochondrial DNA (mtDNA), indicating that mitochondrial damage and mitophagy do not contribute to the inflammation response during NDV infection.
Keyphrases
- oxidative stress
- induced apoptosis
- diabetic rats
- cell death
- endoplasmic reticulum stress
- cell cycle arrest
- signaling pathway
- mitochondrial dna
- dna damage
- high glucose
- disease virus
- drug induced
- poor prognosis
- reactive oxygen species
- copy number
- liver injury
- rheumatoid arthritis
- infectious diseases
- long non coding rna
- transcription factor