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三叉神经节中的巨噬细胞促进大鼠下颌下神经损伤后的异位机械性超敏反应。

Macrophages in trigeminal ganglion contribute to ectopic mechanical hypersensitivity following inferior alveolar nerve injury in rats.

机构信息

Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8549, Japan.

Department of Physiology, School of Dentistry, Nihon University, 1-8-13 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8310, Japan.

出版信息

J Neuroinflammation. 2017 Dec 16;14(1):249. doi: 10.1186/s12974-017-1022-3.

Abstract

BACKGROUND

Accidental mandibular nerve injury may occur during tooth extraction or implant procedures, causing ectopic orofacial pain. The exact mechanisms underlying ectopic orofacial pain following mandibular nerve injury is still unknown. Here, we investigated the role of macrophages and tumor necrosis factor alpha (TNFα) in the trigeminal ganglion (TG) in ectopic orofacial pain following inferior alveolar nerve transection (IANX).

METHODS

IANX was performed and the mechanical head-withdrawal threshold (MHWT) in the whisker pad skin ipsilateral to IANX was measured for 15 days. Expression of Iba1 in the TG was examined on day 3 after IANX, and the MHWT in the whisker pad skin ipsilateral to IANX was measured following successive intra-ganglion administration of the macrophage depletion agent liposomal clodronate Clophosome-A (LCCA). TNFα expression in the TG and the MHWT in the whisker pad skin ipsilateral to IANX following successive intra-ganglion administration of the TNFα blocker etanercept were measured on day 3 after IANX, and tumor necrosis factor receptor-1 (TNFR1) immunoreactive (IR) cells in the TG were analyzed immunohistochemically on day 3.

RESULTS

The MHWT in the whisker pad skin was significantly decreased for 15 days, and the number of Iba1-IR cells was significantly increased in the TG on day 3 after IANX. Successive intra-ganglion administration of the macrophage depletion agent LCCA significantly reduced the increased number of Iba1-IR cells in the TG and reversed the IANX-induced decrease in MHWT in the whisker pad skin. TNFα expression was increased in the TG on day 3 after IANX and was reduced following successive intra-ganglion administration of the TNFα inhibitor etanercept. The decreased MHWT was also recovered by etanercept administration, and TNFR1-IR cells in the TG were increased on day 3 following IANX.

CONCLUSIONS

These findings suggest that signaling cascades resulting from the production of TNFα by infiltrated macrophages in the TG contributes to the development of ectopic mechanical allodynia in whisker pad skin following IANX.

摘要

背景

下颌神经损伤可能发生在拔牙或种植手术过程中,导致异位口腔面部疼痛。下颌神经损伤后异位口腔面部疼痛的确切机制尚不清楚。在这里,我们研究了巨噬细胞和肿瘤坏死因子 α(TNFα)在三叉神经节(TG)中的作用在下颌神经切断(IANX)后异位口腔面部疼痛。

方法

进行 IANX,并测量对侧下颌神经切断(IANX)的胡须垫皮肤的机械头部回缩阈值(MHWT)15 天。在 IANX 后第 3 天检查 TG 中的 Iba1 表达,并在 TG 中连续给予巨噬细胞耗竭剂脂质体氯膦酸盐 Clophosome-A(LCCA)后测量对侧胡须垫皮肤的 MHWT。在 IANX 后第 3 天测量 TG 中 TNFα 表达和对侧胡须垫皮肤的 MHWT,并在第 3 天进行免疫组织化学分析 TG 中的肿瘤坏死因子受体-1(TNFR1)免疫反应(IR)细胞。

结果

胡须垫皮肤的 MHWT 显著降低 15 天,IANX 后第 3 天 TG 中 Iba1-IR 细胞数量显著增加。连续给予 TG 中巨噬细胞耗竭剂 LCCA 可显著减少 TG 中 Iba1-IR 细胞的增加数量,并逆转 IANX 引起的胡须垫皮肤 MHWT 降低。IANX 后第 3 天 TG 中 TNFα 表达增加,给予 TNFα 抑制剂依那西普后减少。依那西普给药也恢复了 MHWT 的降低,IANX 后第 3 天 TG 中 TNFR1-IR 细胞增加。

结论

这些发现表明,TG 中浸润巨噬细胞产生的 TNFα 信号级联反应导致 IANX 后胡须垫皮肤异位机械性感觉过敏的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eac8/5732495/65767716282a/12974_2017_1022_Fig1_HTML.jpg

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