Zaratin Paola F, Quattrini Angelo, Previtali Stefano C, Comi Giancarlo, Hervieu Guillaume, Scheideler Mark A
Department of Neurobiology Research, GlaxoSmithKline Pharmaceuticals, Milan, Italy.
Mol Cell Neurosci. 2005 Jan;28(1):55-63. doi: 10.1016/j.mcn.2004.08.010.
The human 7-transmembrane receptor GPR7 has sequence similarity to opioid and somatostatin receptors, and can be activated by the recently discovered neuropeptides NPB and NPW. This receptor is highly expressed in the nervous system, with suggested roles in neuroendocrine events and pain signaling. In this study, we investigated whether the GPR7 receptor is expressed in the peripheral nervous system under normal and pathological conditions. A low level of GPR7 receptor was observed in myelin-forming Schwann cells in both normal human and rat nerve, and in primary rat Schwann cell cultures. Peripheral nerve samples taken from patients exhibiting inflammatory/immune-mediated neuropathies showed a dramatic increase of GPR7 receptor expression restricted to myelin-forming Schwann cells. Complementary animal models of immune-inflammatory and ligation-induced nerve injury and neuropathic pain similarly exhibited an increased myelin-associated expression of GPR7 receptor. These results suggest a relationship between the pathogenesis of inflammatory/immune-mediated neuropathies, GPR7 receptor expression, and pain transmission.
人类7跨膜受体GPR7与阿片样物质和生长抑素受体具有序列相似性,并且可被最近发现的神经肽NPB和NPW激活。该受体在神经系统中高度表达,提示其在神经内分泌事件和疼痛信号传导中发挥作用。在本研究中,我们调查了GPR7受体在正常和病理条件下是否在外周神经系统中表达。在正常人和大鼠神经的形成髓鞘的施万细胞以及原代大鼠施万细胞培养物中均观察到低水平的GPR7受体。取自表现出炎症/免疫介导的神经病变患者的外周神经样本显示,GPR7受体表达急剧增加,且仅限于形成髓鞘的施万细胞。免疫炎症和结扎诱导的神经损伤及神经性疼痛的互补动物模型同样显示,GPR7受体的髓鞘相关表达增加。这些结果提示炎症/免疫介导的神经病变的发病机制、GPR7受体表达与疼痛传递之间存在关联。