Centre des Sciences du Goût et de l'Alimentation, UMR1324 INRA, UMR6265 CNRS, Université de Bourgogne, Agrosup Dijon, F-21000 Dijon, France.
Neurosci Lett. 2011 Nov 14;505(2):180-5. doi: 10.1016/j.neulet.2011.10.018. Epub 2011 Oct 13.
Transporters, such as multidrug resistance P-glycoproteins (MDR), multidrug resistance-related proteins (MRP) and organic anion transporters (OATs), are involved in xenobiotic metabolism, particularly the cellular uptake or efflux of xenobiotics (and endobiotics) or their metabolites. The olfactory epithelium is exposed to both inhaled xenobiotics and those coming from systemic circulation. This tissue has been described as a pathway for xenobiotics to the brain via olfactory perineural space. Thereby, olfactory transporters and xenobiotic metabolizing enzymes, dedicated to the inactivation and the elimination of xenobiotics, have been involved in the toxicological protection of the brain, the olfactory epithelium itself and the whole body. These proteins could also have a role in the preservation of the olfactory sensitivity by inactivation and clearance of the excess of odorant molecules from the perireceptor space. The goal of the present study was to increase our understanding of the expression and the localization of transporters in this tissue. For most of the studied transporters, we observed an opposite mRNA expression pattern (RT-PCR) in the olfactory epithelium compared to the liver, which is considered to be the main metabolic organ. Olfactory epithelium mainly expressed efflux transporters (MRP, MDR). However, a similar pattern was observed between the olfactory epithelium and the olfactory bulb. We also demonstrate distinct cellular immunolocalization of the transporters in the olfactory epithelium. As previously reported, Mrp1 was mainly found in the supranuclear portions of supporting cells. In addition, Mrp3 and Mrp5 proteins, which were detected for the first time in olfactory epithelium, were localized to the olfactory neuron layer, while Mdr1 was localized to the capillary endothelium of lymphatic vessels in the subepithelial region. The pattern of expression and the distinct localization of the olfactory transporters showed in this work may highlight on their specific function in the whole olfactory epithelium.
转运蛋白,如多药耐药 P 糖蛋白 (MDR)、多药耐药相关蛋白 (MRP) 和有机阴离子转运蛋白 (OAT),参与外源性物质代谢,特别是外源性物质(和内源性物质)或其代谢物的细胞摄取或外排。嗅上皮暴露于吸入的外源性物质和来自全身循环的外源性物质。该组织被描述为外源性物质通过嗅神经周间隙进入大脑的途径。因此,专门用于外源性物质失活和消除的嗅觉转运蛋白和外源性物质代谢酶参与了大脑、嗅上皮本身和全身的毒理学保护。这些蛋白质还可以通过失活和清除过量的嗅敏分子从受体外空间来发挥嗅觉敏感性的保护作用。本研究的目的是增加我们对该组织中转运蛋白表达和定位的理解。对于大多数研究的转运蛋白,我们观察到嗅上皮的 mRNA 表达模式(RT-PCR)与肝脏相反,肝脏被认为是主要的代谢器官。嗅上皮主要表达外排转运蛋白(MRP、MDR)。然而,在嗅上皮和嗅球之间观察到类似的模式。我们还证明了转运蛋白在嗅上皮中的不同细胞免疫定位。如前所述,Mrp1 主要存在于支持细胞的核上部分。此外,首次在嗅上皮中检测到的 Mrp3 和 Mrp5 蛋白定位于嗅神经元层,而 Mdr1 定位于上皮下区域淋巴管的毛细血管内皮。本研究中观察到的嗅觉转运蛋白的表达模式和独特定位可能突出了它们在整个嗅上皮中的特定功能。