基于WGCNA探讨葛根素对呕吐毒素诱导C6细胞损伤的保护作用OA北大核心CSTPCD
Exploring the Protective Effect of Puerarin on Deoxynivalenol-induced C6 Cell Injury Based on WGCNA
[目的]利用呕吐毒素(deoxynivalenol,DON)构建C6 细胞损伤模型,分析葛根素(puerarin,PUE)对DON诱导C6 细胞损伤的保护作用机制.[方法]通过RNA测序(RNA-seq)和加权基因共表达网络分析(weighted gene co-expression network analysis,WGCNA),挖掘与PUE缓解DON诱导C6 细胞损伤最相关的关键模块和关键核心靶点基因,探究PUE缓解DON诱导的神经毒性作用的分子机制.[结果]PUE可以显著抑制DON诱导的C6 细胞活力下降,对损伤的C6 细胞形态有所恢复,可有效缓解DON诱导的C6细胞损伤.RNA-seq和WGCNA结果表明,Blue模块是与PUE缓解DON诱导C6细胞损伤表型最相关的关键模块,从中筛选出S100a11、Pdia3、Hsp90b1 等基因是PUE发挥对DON诱导C6 细胞损伤保护作用的关键核心基因.[结论]PUE可能是通过靶向关键核心基因参与内质网中的蛋白质加工途径从而缓解DON诱导的C6 细胞损伤.
[Objective]The experiment used deoxynivalenol(DON)to construct a C6 cell injury model and analyzed the protective mechanism of puerarin(PUE)in alleviating DON-induced C6 cell injury.[Method]By using RNA sequencing(RNA-seq)and weighted gene co expression network analysis(WGCNA),we aimed to identify the key modules and core target genes,which was most closely related to the alleviation of PUE on DON-induced C6 cell injury.Furthermore,we explored the molecular mechanism of PUE in alleviating DON-induced neurotoxicity.[Result]The PUE significantly inhibited the decrease in the cell viability induced by DON,restored the morphology of damaged C6 cells,and effectively alleviated DON-induced cytotoxicity.The RNA seq and WGCNA results indicated that the Blue module was the most relevant key module to the alleviation of PUE on DON-induced C6 cell injury,and S100a11,Pdia3 and Hsp90b1 genes were selected as the key core genes.[Conclusion]These results suggest that PUE may alleviate DON-induced C6 cell injury by targeting key core genes and regulating in endoplasmic reticulum signaling pathway.
赵海平;刘林;王昕璐;岳鹏飞;孔维军;王蒙
江西中医药大学中医学院,南昌 330004江西中医药大学中医学院,南昌 330004||北京市农林科学院质量标准与检测技术研究所,北京 100097北京市农林科学院质量标准与检测技术研究所,北京 100097江西中医药大学现代中药制剂教育部重点实验室,南昌 330004
呕吐毒素葛根素加权基因共表达网络分析C6细胞
deoxynivalenolpuerarinweighted gene co-expression network analysis(WGCNA)C6 cell
《生物技术通报》 2024 (009)
301-310 / 10
国家自然科学基金项目(32372453),北京市农林科学院杰出科学家培育专项项目(JKZX202403),江西中医药大学现代中药制剂教育部重点实验室开放基金资助项目(zdsys-202109)
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