Expression and differential localization of xenobiotic transporters in the rat olfactory neuro-epithelium

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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Animals
  • Gene Expression Regulation / physiology
  • Hepatocytes / cytology
  • Hepatocytes / metabolism
  • Liver / cytology
  • Liver / metabolism
  • Lymphatic Vessels / metabolism
  • Lymphatic Vessels / ultrastructure
  • Male
  • Multidrug Resistance-Associated Proteins / genetics
  • Multidrug Resistance-Associated Proteins / metabolism
  • Odorants
  • Olfactory Mucosa / cytology
  • Olfactory Mucosa / drug effects
  • Olfactory Mucosa / metabolism*
  • Olfactory Receptor Neurons / cytology
  • Olfactory Receptor Neurons / drug effects
  • Olfactory Receptor Neurons / metabolism*
  • Protein Transport / genetics
  • Rats
  • Rats, Wistar
  • Receptors, Odorant / genetics
  • Receptors, Odorant / metabolism
  • Smell / genetics
  • Xenobiotics / metabolism*


  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Abcc5 protein, rat
  • Multidrug Resistance-Associated Proteins
  • Receptors, Odorant
  • Xenobiotics
  • multidrug resistance-associated protein 3
  • multidrug resistance-associated protein 1