School of Anesthesiology, Jiangsu Province Key Laboratory of Anesthesiology, Xuzhou Medical University, 209 Tongshan Road, Xuzhou, 221004, China.
Department of Pharmacy, The Affiliated Hospital of Xuzhou Medical University, Xuzhou Medical University, Xuzhou, 221002, China.
Cell Mol Neurobiol. 2020 Oct;40(7):1117-1131. doi: 10.1007/s10571-020-00797-3. Epub 2020 Jan 27.
Chronic morphine-induced antinociceptive tolerance is a major unresolved issue in clinical practices, which is associated with microglia activation in the spinal cord. E3 ubiquitin ligase Pellino1 (Peli1) is known to be an important microglia-specific regulator. However, it is unclear whether Peli1 is involved in morphine tolerance. Here, we found that Peli1 levels in the spinal cord were significantly elevated in morphine tolerance mouse model. Notably, Peli1 was expressed in a great majority of microglia in the spinal dorsal horn, while downregulation of spinal Peli1 attenuated the development of morphine tolerance and associated hyperalgesia. Our biochemical data revealed that morphine tolerance-induced increase in Peli1 was accompanied by spinal microglia activation, activation of mitogen-activated protein kinase (MAPK) signaling, and production of proinflammatory cytokines. Peli1 additionally was found to promote K63-linked ubiquitination of tumor necrosis factor receptor-associated factor 6 (TRAF6) in the spinal cord after repeated morphine treatment. Furthermore, knocking down Peli1 in cultured BV2 microglial cells significantly attenuated inflammatory reactions in response to morphine challenge. Therefore, we conclude that the upregulation of Peli1 in the spinal cord plays a curial role in the development of morphine tolerance via Peli1-dependent mobilization of spinal microglia, activation of MAPK signaling, and production of proinflammatory cytokines. Modulation of Peli1 may be a potential strategy for the prevention of morphine tolerance.
慢性吗啡诱导的抗伤害性耐受是临床实践中的一个未解决的主要问题,与脊髓中小胶质细胞的激活有关。E3 泛素连接酶 Pellino1(Peli1)已知是一种重要的小胶质细胞特异性调节剂。然而,尚不清楚 Peli1 是否参与吗啡耐受。在这里,我们发现吗啡耐受小鼠模型中脊髓 Peli1 水平显著升高。值得注意的是,Peli1 在脊髓背角的大多数小胶质细胞中表达,而脊髓 Peli1 的下调减弱了吗啡耐受的发展和相关的痛觉过敏。我们的生化数据显示,吗啡耐受诱导的 Peli1 增加伴随着脊髓小胶质细胞的激活、丝裂原活化蛋白激酶(MAPK)信号的激活和促炎细胞因子的产生。此外,在重复吗啡处理后,还发现 Peli1 促进了脊髓中肿瘤坏死因子受体相关因子 6(TRAF6)的 K63 连接泛素化。进一步,在培养的 BV2 小胶质细胞中敲低 Peli1 显著减弱了对吗啡刺激的炎症反应。因此,我们得出结论,脊髓中 Peli1 的上调通过 Peli1 依赖性募集脊髓小胶质细胞、激活 MAPK 信号和产生促炎细胞因子,在吗啡耐受的发展中起着关键作用。调节 Peli1 可能是预防吗啡耐受的一种潜在策略。