Equipe Neurophysiologie de la Peripherie des Systèmes Chimiosensoriels, Centre des Sciences du Goût et de l'Alimentation, CNRS UMR 6265, INRA, Université de Bourgogne, Dijon, France.
PLoS One. 2012;7(5):e36167. doi: 10.1371/journal.pone.0036167. Epub 2012 May 1.
P-glycoprotein (Pgp) and multidrug resistance-associated protein (MRP1) are membrane transporter proteins which function as efflux pumps at cell membranes and are considered to exert a protective function against the entry of xenobiotics. While evidence for Pgp and MRP transporter activity is reported for olfactory tissue, their possible interaction and participation in the olfactory response has not been investigated.
Functional activity of putative MDR transporters was assessed by means of the fluorometric calcein acetoxymethyl ester (calcein-AM) accumulation assay on acute rat and mouse olfactory tissue slices. Calcein-AM uptake was measured as fluorescence intensity changes in the presence of Pgp or MRP specific inhibitors. Epifluorescence microscopy measured time course analysis in the olfactory epithelium revealed significant inhibitor-dependent calcein uptake in the presence of each of the selected inhibitors. Furthermore, intracellular calcein accumulation in olfactory receptor neurons was also significantly increased in the presence of either one of the Pgp or MRP inhibitors. The presence of Pgp or MRP1 encoding genes in the olfactory mucosa of rat and mouse was confirmed by RT-PCR with appropriate pairs of species-specific primers. Both transporters were expressed in both newborn and adult olfactory mucosa of both species. To assess a possible involvement of MDR transporters in the olfactory response, we examined the electrophysiological response to odorants in the presence of the selected MDR inhibitors by recording electroolfactograms (EOG). In both animal species, MRPs inhibitors induced a marked reduction of the EOG magnitude, while Pgp inhibitors had only a minor or no measurable effect.
The findings suggest that both Pgp and MRP transporters are functional in the olfactory mucosa and in olfactory receptor neurons. Pgp and MRPs may be cellular constituents of olfactory receptor neurons and represent potential mechanisms for modulation of the olfactory response.
P-糖蛋白(Pgp)和多药耐药相关蛋白 1(MRP1)是细胞膜转运蛋白,作为细胞膜上的外排泵发挥作用,被认为对异源物的进入具有保护作用。虽然已经有报道称嗅组织中存在 Pgp 和 MRP 转运体活性,但它们的可能相互作用及其在嗅觉反应中的参与尚未得到研究。
通过荧光比色法测定急性大鼠和小鼠嗅组织切片中潜在的 MDR 转运体的功能活性。在存在 Pgp 或 MRP 特异性抑制剂的情况下,通过 calcein-AM 摄取测定 calcein-AM 摄取。荧光显微镜测量嗅上皮中的时程分析显示,在每种选定抑制剂的存在下,均存在显著的抑制剂依赖性 calcein 摄取。此外,在存在任何一种 Pgp 或 MRP 抑制剂的情况下,嗅感觉神经元中的细胞内 calcein 积累也显著增加。通过使用适当的种特异性引物的 RT-PCR 证实了 Pgp 或 MRP1 编码基因在大鼠和小鼠嗅黏膜中的存在。两种转运体均在两种动物的新生和成年嗅黏膜中表达。为了评估 MDR 转运体在嗅觉反应中的可能参与,我们通过记录电嗅觉图(EOG),在存在选定的 MDR 抑制剂的情况下,检查了对气味剂的电生理反应。在两种动物物种中,MRP 抑制剂诱导 EOG 幅度明显降低,而 Pgp 抑制剂仅具有较小或可测量的影响。
这些发现表明 Pgp 和 MRP 转运体在嗅黏膜和嗅感觉神经元中均具有功能。Pgp 和 MRPs 可能是嗅感觉神经元的细胞成分,代表了调节嗅觉反应的潜在机制。