Momentum Laboratory of Molecular Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Szigony utca 43., H-1083, Budapest, Hungary.
Eur J Neurosci. 2014 Feb;39(3):419-34. doi: 10.1111/ejn.12470.
Monoacylglycerol lipase (MGL) is a multifunctional serine hydrolase, which terminates anti-nociceptive endocannabinoid signaling and promotes pro-nociceptive prostaglandin signaling. Accordingly, both acute nociception and its sensitization in chronic pain models are prevented by systemic or focal spinal inhibition of MGL activity. Despite its analgesic potential, the neurobiological substrates of beneficial MGL blockade have remained unexplored. Therefore, we examined the regional, cellular and subcellular distribution of MGL in spinal circuits involved in nociceptive processing. All immunohistochemical findings obtained with light, confocal or electron microscopy were validated in MGL-knockout mice. Immunoperoxidase staining revealed a highly concentrated accumulation of MGL in the dorsal horn, especially in superficial layers. Further electron microscopic analysis uncovered that the majority of MGL-immunolabeling is found in axon terminals forming either asymmetric glutamatergic or symmetric γ-aminobutyric acid/glycinergic synapses in laminae I/IIo. In line with this presynaptic localization, analysis of double-immunofluorescence staining by confocal microscopy showed that MGL colocalizes with neurochemical markers of peptidergic and non-peptidergic nociceptive terminals, and also with markers of local excitatory or inhibitory interneurons. Interestingly, the ratio of MGL-immunolabeling was highest in calcitonin gene-related peptide-positive peptidergic primary afferents, and the staining intensity of nociceptive terminals was significantly reduced in MGL-knockout mice. These observations highlight the spinal nociceptor synapse as a potential anatomical site for the analgesic effects of MGL blockade. Moreover, the presence of MGL in additional terminal types raises the possibility that MGL may play distinct regulatory roles in synaptic endocannabinoid or prostaglandin signaling according to its different cellular locations in the dorsal horn pain circuitry.
单酰甘油脂肪酶(MGL)是一种多功能丝氨酸水解酶,可终止抗伤害性内源性大麻素信号传递,并促进促伤害性前列腺素信号传递。因此,全身性或局部脊髓抑制 MGL 活性可防止急性伤害感受和慢性疼痛模型中的伤害感受敏化。尽管具有镇痛潜力,但有益的 MGL 阻断的神经生物学基础仍未得到探索。因此,我们研究了参与伤害感受处理的脊髓回路中 MGL 的区域、细胞和亚细胞分布。使用光学、共聚焦或电子显微镜获得的所有免疫组织化学发现均在 MGL 敲除小鼠中得到验证。免疫过氧化物酶染色显示 MGL 在背角中高度集中,特别是在浅层。进一步的电子显微镜分析揭示了大多数 MGL 免疫标记位于形成 I/IIo 层中不对称谷氨酸能或对称 γ-氨基丁酸/甘氨酸能突触的轴突末端。与这种突触前定位一致,通过共聚焦显微镜分析双重免疫荧光染色显示,MGL 与肽能和非肽能伤害性末端的神经化学标志物以及局部兴奋性或抑制性中间神经元的标志物共定位。有趣的是,MGL 免疫标记的比率在降钙素基因相关肽阳性肽能初级传入纤维中最高,并且 MGL 敲除小鼠中伤害性末端的染色强度显著降低。这些观察结果突出了脊髓伤害感受器突触作为 MGL 阻断镇痛作用的潜在解剖部位。此外,MGL 存在于其他末端类型中,这表明 MGL 可能根据其在背角疼痛回路中的不同细胞位置,在突触内源性大麻素或前列腺素信号传递中发挥不同的调节作用。