CXCL8 Knockout: A Key to Resisting Pasteurella multocida Toxin-Induced Cytotoxicity.
Jianlin YuanQin ZhaoJinfeng LiYiping WenRui WuShan ZhaoYi-Fei LangQi-Gui YanXiaobo HuangSenyan DuSan-Jie CaoPublished in: International journal of molecular sciences (2024)
Pasteurella multocida , a zoonotic pathogen that produces a 146-kDa modular toxin (PMT), causes progressive atrophic rhinitis with severe turbinate bone degradation in pigs. However, its mechanism of cytotoxicity remains unclear. In this study, we expressed PMT, purified it in a prokaryotic expression system, and found that it killed PK15 cells. The host factor CXCL8 was significantly upregulated among the differentially expressed genes in a transcriptome sequencing analysis and qPCR verification. We constructed a CXCL8-knockout cell line with a CRISPR/Cas9 system and found that CXCL8 knockout significantly increased resistance to PMT-induced cell apoptosis. CXCL8 knockout impaired the cleavage efficiency of apoptosis-related proteins, including Caspase3, Caspase8, and PARP1, as demonstrated with Western blot. In conclusion, these findings establish that CXCL8 facilitates PMT-induced PK15 cell death, which involves apoptotic pathways; this observation documents that CXCL8 plays a key role in PMT-induced PK15 cell death.
Keyphrases
- cell death
- cell cycle arrest
- high glucose
- diabetic rats
- induced apoptosis
- crispr cas
- drug induced
- escherichia coli
- oxidative stress
- endoplasmic reticulum stress
- poor prognosis
- single cell
- multiple sclerosis
- signaling pathway
- dna damage
- genome editing
- early onset
- transcription factor
- body composition
- wastewater treatment
- long non coding rna
- postmenopausal women