Department of Rehabilitation, Huai'an Second People's Hospital, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223000, Jiangsu, China.
Department of Rheumatology and Immunology, Huai'an Traditional Chinese Medicine Hospital, Huai'an 223000, Jiangsu, China.
Crit Rev Eukaryot Gene Expr. 2024;34(7):17-27. doi: 10.1615/CritRevEukaryotGeneExpr.2024053243.
This study aimed to investigate the effects of electroacupuncture (EA) treatment on Parkinson's disease (PD). 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) administration was used establish PD mice model. The number of neurons is determined by TH staining. mRNA expression is detected by RT-qPCR. Protein expression was detected by Western blot. Gene expression is determined by immunofluorescence and immunohistochemistry. The functions of neurons are determined by TUNEL and flow cytometry assay. The binding sites of nuclear factor kappa B (NF-κB) RELA on the promoter of NLRP3 are predicted by JASPAR and verified by luciferase and ChIP assays. The results showed that EA treatment improves motor dysfunction in patients with PD. In vivo assays show that MPTP administration induces the loss of neurons in mice, which is restored by EA treatment. Moreover, EA treatment alleviates motor deficits in MPTP-induced PD mice. EA treatment also inhibits the enrichment of pro-inflammatory cytokines and lactodehydrogenase and suppresses neuronal pyroptosis. EA treatment increases the expression of METTL9. However, METTL9 deficiency dampens the effects of EA treatment and induces neuronal pyroptosis. Additionally, METTL9 promotes histidine methylation of NF-κB RELA, resulting the inhibition of epigenetic transcription of NLRP3. EA treatment restores neuronal function and improves motor dysfunction via promoting METTL9 histidine methylation of NF-κB/ NLRP3 signaling.
本研究旨在探讨电针(EA)治疗对帕金森病(PD)的影响。使用 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)建立 PD 小鼠模型。通过 TH 染色确定神经元数量。通过 RT-qPCR 检测 mRNA 表达。通过 Western blot 检测蛋白表达。通过免疫荧光和免疫组化检测基因表达。通过 TUNEL 和流式细胞术测定神经元功能。通过 JASPAR 预测核因子 kappa B(NF-κB)RELA 结合在 NLRP3 启动子上的结合位点,并通过荧光素酶和 ChIP 测定验证。结果表明,EA 治疗可改善 PD 患者的运动功能障碍。体内实验表明,MPTP 给药诱导小鼠神经元丢失,EA 治疗可恢复。此外,EA 治疗可减轻 MPTP 诱导的 PD 小鼠的运动缺陷。EA 治疗还抑制促炎细胞因子和乳酸脱氢酶的富集,并抑制神经元细胞焦亡。EA 治疗增加 METTL9 的表达。然而,METTL9 缺乏会抑制 EA 治疗的效果并诱导神经元细胞焦亡。此外,METTL9 促进 NF-κB RELA 的组氨酸甲基化,从而抑制 NLRP3 的表观转录。EA 治疗通过促进 NF-κB/NLRP3 信号通路中 METTL9 组氨酸甲基化来恢复神经元功能并改善运动功能障碍。