Mousa Shaaban A, Shaqura Mohammed, Tafelski Sascha, Wandrey Jan David, Celik Özgür, Treskatsch Sascha, Schäfer Michael
Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Anaesthesiology and Intensive Care Medicine, Charité Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Anaesthesiology and Intensive Care Medicine, Charité Campus Mitte and Campus Virchow Clinic, Charitéplatz 1, 10117 Berlin, Germany.
Cells. 2025 May 11;14(10):694. doi: 10.3390/cells14100694.
The presence and function of the opioidergic system in sensory dorsal root ganglia (DRG) was demonstrated in various animal models of pain. To endorse recent functional and transcriptional evidence of opioid receptors in human DRG, this study compared morphological and transcriptional evidence in human and rat DRG using immunofluorescence confocal microscopy and mRNA transcript analysis. Specifically, it examined the neuronal expression of mu (MOR), delta (DOR), and kappa (KOR) opioid receptors, opioid peptide precursors (POMC, PENK, and PDYN), and key pain-signaling molecules. The results demonstrate abundant immunoreactivity in human DRG for key pain transduction receptors, including the thermosensitive ion channels TRPV1, TRPV4 and TRPA1, mechanosensitive PIEZO1 and PIEZO2, and the nociceptive-specific Nav1.8. They colocalized with calcitonin gene-related peptide (CGRP), a marker for peptidergic sensory neurons. Within this same subpopulation, we identified MOR, DOR, and KOR, while their ligand precursors were less abundant. Notably, the mRNA transcripts of MOR and PENK in human DRG were highest among the opioid-related genes; however, they were considerably lower than those of key pain-signaling molecules. These findings were corroborated by functional evidence in demonstrating the fentanyl-induced inhibition of voltage-gated calcium currents in rat DRG, which was antagonized by naloxone. The immunohistochemical and transcriptional demonstration of opioid receptors and their endogenous ligands in both human and rat DRG support recent electrophysiologic and in situ hybridization evidence in human DRG and confirms their potential as analgesic targets. This peripherally targeted approach has the advantage of mitigating central opioid-related side effects, endorsing the potential of future translational pain research from rodent models to humans.
在各种疼痛动物模型中已证实感觉背根神经节(DRG)中存在阿片肽能系统及其功能。为了支持人类DRG中阿片受体的最新功能和转录证据,本研究使用免疫荧光共聚焦显微镜和mRNA转录分析比较了人类和大鼠DRG中的形态学和转录证据。具体而言,研究了μ(MOR)、δ(DOR)和κ(KOR)阿片受体、阿片肽前体(POMC、PENK和PDYN)以及关键疼痛信号分子的神经元表达。结果表明,人类DRG中关键疼痛转导受体存在丰富的免疫反应性,包括热敏离子通道TRPV1、TRPV4和TRPA1、机械敏感的PIEZO1和PIEZO2,以及伤害性特异性Nav1.8。它们与降钙素基因相关肽(CGRP)共定位,CGRP是肽能感觉神经元的标志物。在同一亚群中,我们鉴定出了MOR、DOR和KOR,而它们的配体前体含量较少。值得注意的是,人类DRG中MOR和PENK的mRNA转录本在阿片相关基因中最高;然而,它们远低于关键疼痛信号分子的转录本。芬太尼诱导大鼠DRG中电压门控钙电流受到抑制,而纳洛酮可拮抗这种抑制作用,这一功能证据证实了上述发现。人类和大鼠DRG中阿片受体及其内源性配体的免疫组织化学和转录证明支持了人类DRG中最近的电生理学和原位杂交证据,并证实了它们作为镇痛靶点的潜力。这种外周靶向方法具有减轻中枢阿片类药物相关副作用的优势,为未来从啮齿动物模型到人类的转化性疼痛研究提供了潜力。