首页|脊髓背根神经节ZXDC介导CCL2对慢性压迫性神经损伤小鼠神经性疼痛的作用

脊髓背根神经节ZXDC介导CCL2对慢性压迫性神经损伤小鼠神经性疼痛的作用

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目的 探讨脊髓背根神经节(dorsal root ganglion,DRG)中转录因子锌指X连锁复制C(zinc finger X-linked dupli-cated C,ZXDC)介导CCL2/CCR2信号通路对慢性压迫性神经损伤(chronic construction injury model,CCI)诱导神经性疼痛的作用及机制.方法 构建小鼠坐骨神经慢性压迫性损伤模型,免疫荧光染色、Western blot法和实时荧光定量PCR(RT-qPCR)检测正常情况和CCI造模后DRG中ZXDC及CCL2表达变化;将实验动物分为假手术(Sham)组、CCI+AAV-NC组和CCI+AAV-ZXDC siRNA组;Western blot法和免疫荧光染色检测各组小鼠CCI造模后各时间点DRG中ZXDC、CCL2和CCR2表达,RT-qPCR检测DRG中促炎性细胞因子TNF-α和IL-1 β mRNA表达,机械性缩足反射测试检测神经性疼痛行为改变.结果 ZX-DC表达定位在DRG大、中、小神经元.CCI损伤后1~3天DRG中ZXDC和CCL2蛋白和mRNA表达显著增高,CCI后7天二者表达显著降低,ZXDC和CCL2mRNA表达量呈正相关(P均<0.05).CCI后3天,与Sham组比较,CCI+AAV-NC组和CCI+AAV-ZXDC siRNA 组 ZXDC、CCL2、CCR2 蛋白表达、TNF-α 和 IL-1β mRNA 表达显著增高,其中 CCI+AAV-ZXDC siRNA 组较 CCI+AAV-NC 组 ZXDC、CCL2、CCR2 蛋白表达、TNF-α 和 IL-1 β mRNA 显著降低(P均<0.05).与 Sham 组比较,CCI+AAV-ZXDC siRNA组和CCI+AAV-NC组CCI后各时间点机械缩足阈值均显著降低,其中CCI后7天,CCI+AAV-ZXDC siR-NA组机械缩足阈值显著高于CCI+AAV-NC组(P均<0.05).结论 脊髓背根神经节ZXDC基因敲减通过抑制CCL2/CCR2信号通路介导CCI诱导的神经性疼痛.
Effects of ZXDC Mediates CCL2 on Chronic Neuropathic Pain in Spinal Dorsal Root Ganglion
Objective To explore the effect and mechanism of C-C motif chemokine ligand 2(CCL2)/C-C chemokine receptor type 2(CCR2)signaling pathway mediated by ZXDC in spinal dorsal root ganglion(DRG)on neuropathic pain after chronic compressive injury.Methods A chronic compressive injury(CCI)mouse model was established.The expression of ZXDC and CCL2 in DRG was detected by immunofluorescence,Western blot,and real-time fluorescent quantitative PCR(RT-qPCR).The animals were divided in-to sham group,CCI+AAV-NC group,and CCI+AAV-ZXDC siRNA group.Western blot and immunofluorescence were employed to measure the expression of ZXDC,CCL2,and CCR2 in DRG after CCI,and the expression of pro-inflammatory factor TNF-α and IL-1β mRNA was evaluated by RT-qPCR.At last,the paw withdrawal threshold was used to evaluate the changes in neuropathic pain be-havior.Results ZXDC was localized in large,medium,and small DRG neurons.The expression of ZXDC and CCL2 protein and mRNA were significantly increased 1-3 days after CCI,and decreased 7days after CCI in DRG.The expression of ZXDC and CCL2mRNA was positively correlated(P<0.05).3 days after CCI,compared with sham group,ZXDC,CCL2,CCR2 protein expression,TNF-α and IL-1 β mRNA in CCI+AAV-NC group and CCI+AAV-ZXDC siRNA group were significantly increased,and ZXDC,CCL2,CCR2 protein expression,TNF-α and IL-1 β mRNA in CCI+AAV-ZXDC siRNA group were significantly decreased than those in CCI+AAV-NC group(P<0.05).Compared with sham group,the paw withdrawal threshold of CCI+AAV-ZXDC siRNA group and CCI+AAV-NC group were significantly decreased at various time points after CCI,and the withdrawal threshold in CCI+AAV-ZXDC siRNA group was significantly increased than that in CCI+AAV-NC group at 7days after CCI(P<0.05).Conclusion Spinal dorsal root gan-glion ZXDC siRNA can inhibit neuropathic pain after CCI injury by downregulating CCL2/CCR2signaling axis.

Spinal dorsal root ganglionZXDCCCL2Nerve injuryChronic neuropathic pain

李文媛、王晓宇、吕忠孝、刘东明、李艺、王淑影、王莹

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157011 牡丹江医学院神经组织工程研究所

脊髓背根神经节 锌指X连锁复制C CC趋化因子2 神经损伤 慢性神经疼痛

国家自然科学基金资助项目黑龙江省自然科学基金资助项目黑龙江省属高校基本科研业务费项目牡丹江医学院科学基金火炬计划项目牡丹江医学院研究生导师科研专项计划项目

81870977JQ2021H0042021-KYYWF-04692022-MYHJ-012YJSZX2022007

2024

医学研究杂志
中国医学科学院

医学研究杂志

CSTPCD
影响因子:0.702
ISSN:1673-548X
年,卷(期):2024.53(1)
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