NQO1 activity in the main and the accessory olfactory systems correlates with the zonal topography of projection maps

被引:72
作者
Gussing, F [1 ]
Bohm, S [1 ]
机构
[1] Umea Univ, Dept Mol Biol, SE-90187 Umea, Sweden
关键词
DT-diaphorase; gene expression; odorant receptors; olfactory; sensory map; vomeronasal;
D O I
10.1111/j.0953-816X.2004.03331.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mouse olfactory epithelium (OE) is divided into spatial zones, each containing neurons expressing zone-specific subsets of odorant receptor genes. Likewise, the vomeronasal (VN) organ is organized into apical and basal subpopulations of neurons expressing different VN receptor gene families. Axons projecting from the different OE zones and VN subpopulations form synapses within circumscribed regions in the glomerular layer of the olfactory bulb (OB) and accessory olfactory bulb (AOB), respectively. We here show that mature neurons in one defined zone selectively express NADPH:quinone oxidoreductase (NQO1), an enzyme that catalyses reduction of quinones. Immunohistochemistry and in situ hybridization analyses show non-overlapping expression of NQO1 and the Rb8 neural cell adhesion molecule (RNCAM/OCAM) in OE and axon terminals within glomeruli of the OB. In addition, NQO1 immunoreactivity reveals selective, zone-specific axon fasciculation in the olfactory nerve. VN subpopulations do not show complementary patterns of RNCAM and NQO1 immunoreactivity, instead both genes are co-expressed in apical VN neurons that project to the rostral AOB. These results indicate that one division of both the accessory and the main olfactory projection maps are composed of sensory neurons that are specialized to reduce environmental and/or endogenously produced quinones via an NQO1-dependent mechanism. The role of NQO1 in bioactivation of quinoidal drugs also points to a connection between zone-specific NQO1 expression and zone-specific toxicity of certain olfactory toxins.
引用
收藏
页码:2511 / 2518
页数:8
相关论文
共 52 条
[1]   Differential function of RNCAM isoforms in precise target selection of olfactory sensory neurons [J].
Alenius, M ;
Bohm, S .
DEVELOPMENT, 2003, 130 (05) :917-927
[2]   Identification of a novel neural cell adhesion molecule-related gene with a potential role in selective axonal projection [J].
Alenius, M ;
Bohm, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26083-26086
[3]   IMMUNOHISTOCHEMICAL LOCALIZATION OF 6 GLUTATHIONE S-TRANSFERASES WITHIN THE NASAL CAVITY OF THE RAT [J].
BANGER, KK ;
FOSTER, JR ;
LOCK, EA ;
REED, CJ .
ARCHIVES OF TOXICOLOGY, 1994, 69 (02) :91-98
[4]  
Berghard A, 1996, J NEUROSCI, V16, P909
[5]   Ephaptic interactions in the mammalian olfactory system [J].
Bokil, H ;
Laaris, N ;
Blinder, K ;
Ennis, M ;
Keller, A .
JOURNAL OF NEUROSCIENCE, 2001, 21 (20)
[6]   IRREVERSIBLE BINDING AND TOXICITY OF THE HERBICIDE DICHLOBENIL (2,6-DICHLOROBENZONITRILE) IN THE OLFACTORY MUCOSA OF MICE [J].
BRANDT, I ;
BRITTEBO, EB ;
FEIL, VJ ;
BAKKE, JE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (03) :491-501
[7]  
BREITSCHOPF H, 1992, ACTA NEUROPATHOL, V84, P581
[8]   ANTIOXIDANT AND PROOXIDANT FUNCTIONS OF DT-DIAPHORASE IN QUINONE METABOLISM [J].
CADENAS, E .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (02) :127-140
[9]   Neuropilin-2 mediates axonal fasciculation, zonal segregation, but not axonal convergence, of primary accessory olfactory neurons [J].
Cloutier, JF ;
Giger, RJ ;
Koentges, G ;
Dulac, C ;
Kolodkin, AL ;
Ginty, DD .
NEURON, 2002, 33 (06) :877-892
[10]   NADPH DIAPHORASE STAINING WITHIN THE DEVELOPING OLFACTORY BULBS OF NORMAL AND UNILATERALLY ODOR-DEPRIVED RATS [J].
CROULOTTMAN, CE ;
BRUNJES, PC .
BRAIN RESEARCH, 1988, 460 (02) :323-328