Porcher Christophe, Juhem Aurélie, Peinnequin André, Bonaz Bruno
Groupe d'Etude du Stress et des Interactions Neuro-Digestives (EA3744), Department of Gastroenterology, CHU de Grenoble, 217, Grenoble, 38043.
Cell Tissue Res. 2005 Apr;320(1):21-31. doi: 10.1007/s00441-004-1032-1. Epub 2005 Feb 22.
Bombesin receptor subtype-3 (BRS-3), a G-protein-coupled orphan receptor, shares 47% and 55% homology with other known mammalian bombesin receptors. Despite the molecular characterization of BRS-3, its function remains unclear as a consequence of its low affinity for bombesin and the absence of an identified natural ligand. Although the other mammalian bombesin receptors are widely distributed in the gut and central nervous system, expression of BRS-3 in the gastrointestinal tract has not been previously described. We report the expression of BRS-3 mRNA and protein in the tunica muscularis of the rat gastrointestinal tract. The mRNA expression pattern was studied by reverse transcription followed by quantitative polymerase chain reaction. To identify the cellular sites of expression of BRS-3, we performed immunocytochemistry by using a N-terminus-specific affinity-purified antiserum. BRS-3 was found to be widely expressed in the rat gastrointestinal tract at both the mRNA and protein levels. BRS-3-like immunoreactivity (BRS-3-LI) was localized in neurons of the myenteric and submucosal ganglia, being primarily concentrated near the neuronal plasma membrane, and in fibers distributed in the longitudinal and circular muscle layers. In addition, BRS-3-LI was observed in the cell bodies and processes of c-kit+ interstitial cells of Cajal. These data have functional applications for the effects mediated by the activation of BRS-3 on gut motility through distinct neuronal and non-neuronal pathways.
蛙皮素受体亚型-3(BRS-3)是一种G蛋白偶联的孤儿受体,与其他已知的哺乳动物蛙皮素受体具有47%和55%的同源性。尽管对BRS-3进行了分子特征鉴定,但由于其对蛙皮素的亲和力较低且缺乏已确定的天然配体,其功能仍不清楚。虽然其他哺乳动物蛙皮素受体广泛分布于肠道和中枢神经系统,但此前尚未描述BRS-3在胃肠道中的表达情况。我们报告了BRS-3 mRNA和蛋白在大鼠胃肠道肌层中的表达。通过逆转录随后进行定量聚合酶链反应研究mRNA表达模式。为了确定BRS-3的细胞表达位点,我们使用N端特异性亲和纯化抗血清进行免疫细胞化学。发现BRS-3在大鼠胃肠道的mRNA和蛋白水平均广泛表达。BRS-3样免疫反应性(BRS-3-LI)定位于肌间神经节和黏膜下神经节的神经元中,主要集中在神经元质膜附近,以及分布在纵行和环行肌层的纤维中。此外,在Cajal间质细胞的细胞体和突起中观察到BRS-3-LI。这些数据对于通过不同的神经元和非神经元途径激活BRS-3介导的对肠道运动的影响具有功能应用价值