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三叉神经感觉系统中的 TNFα 对于颞下颌关节疼痛至关重要。

TNFα in the Trigeminal Nociceptive System Is Critical for Temporomandibular Joint Pain.

机构信息

Department of Anesthesiology, The Second Affiliated Hospital at Zhengzhou University School of Medicine, 2 Jingba Rd, Zhengzhou, 450000, Henan, China.

Department of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, Texas, USA.

出版信息

Mol Neurobiol. 2019 Jan;56(1):278-291. doi: 10.1007/s12035-018-1076-y. Epub 2018 Apr 25.

DOI:10.1007/s12035-018-1076-y
PMID:29696511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6698364/
Abstract

Previous studies have shown that tumor necrosis factor alpha (TNFα) is significantly increased in complete Freund's adjuvant (CFA)-treated temporomandibular joint (TMJ) tissues. However, it is unclear whether TNFα in the trigeminal nociceptive system contributes to the development of TMJ pain. In the present study, we investigated the role of TNFα in trigeminal ganglia (TG) and spinal trigeminal nucleus caudalis (Sp5C) in CFA-induced inflammatory TMJ pain. Intra-TMJ injection of CFA (10 μl, 5 mg/ml) induced inflammatory pain in the trigeminal nerve V2- and V3-innervated skin areas of WT mice, which was present on day 1 after CFA and persisted for at least 10 days. TNFα in both TG and Sp5C of WT mice was upregulated after CFA injection. The CFA-induced TMJ pain was significantly inhibited in TNFα KO mice. The immunofluorescence staining showed that intra-TMJ CFA injection not only enhanced co-localization of TNFα with Iba1 (a marker for microglia) in both TG and Sp5C but also markedly increased the expression of TNFα in the Sp5C neurons. By the methylated DNA immunoprecipitation assay, we also found that DNA methylation at the TNF gene promoter region in the TG was dramatically diminished after CFA injection, indicating that epigenetic regulation may be involved in the CFA-enhanced TNFα expression in our model. Our results suggest that TNFα in the trigeminal nociceptive system plays a critical role in CFA-induced inflammatory TMJ pain.

摘要

先前的研究表明,肿瘤坏死因子-α(TNFα)在完全弗氏佐剂(CFA)治疗的颞下颌关节(TMJ)组织中显著增加。然而,尚不清楚三叉神经伤害感受系统中的 TNFα是否有助于 TMJ 疼痛的发展。在本研究中,我们研究了 TNFα在 CFA 诱导的炎症性 TMJ 疼痛中的三叉神经节(TG)和脊髓三叉神经核尾侧(Sp5C)中的作用。TMJ 内注射 CFA(10 μl,5 mg/ml)可诱导 WT 小鼠三叉神经 V2 和 V3 支配皮肤区域的炎性疼痛,该疼痛在 CFA 后第 1 天出现,并持续至少 10 天。WT 小鼠 TG 和 Sp5C 中的 TNFα在 CFA 注射后上调。TNFα KO 小鼠的 CFA 诱导的 TMJ 疼痛明显受到抑制。免疫荧光染色显示,TMJ 内 CFA 注射不仅增强了 TG 和 Sp5C 中 TNFα与 Iba1(小胶质细胞标志物)的共定位,而且还显著增加了 Sp5C 神经元中 TNFα的表达。通过甲基化 DNA 免疫沉淀测定,我们还发现 CFA 注射后 TG 中 TNF 基因启动子区域的 DNA 甲基化明显减少,表明表观遗传调控可能参与了我们模型中 CFA 增强的 TNFα表达。我们的结果表明,三叉神经伤害感受系统中的 TNFα在 CFA 诱导的炎症性 TMJ 疼痛中起着关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/eb7cc1065a5a/nihms-1044841-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/5e02aeeb0234/nihms-1044841-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/baf8730ab205/nihms-1044841-f0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/eb7cc1065a5a/nihms-1044841-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/5e02aeeb0234/nihms-1044841-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/034f3bb5ca51/nihms-1044841-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/035a082b509c/nihms-1044841-f0003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef72/6698364/eb7cc1065a5a/nihms-1044841-f0009.jpg

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