ABSTRACT
Olfactory sexual dimorphism has mainly been described in the vomeronasal system, in relation to reproductive behavior, while evidence of sexual dimorphism in the main olfactory bulb (OB) remains scarce. There are no data indicating sex-related differences in the neurochemistry of intrinsic olfactory elements. Neurocalcin (NC) is a calcium-binding protein that is expressed in specific neuronal populations of the central nervous system. Here we analyzed by immunohistochemistry the NC-containing neurons in the mouse main OB, comparing both their quantities and their locations between male and female animals. NC cell density was higher in males than in females in specific locations of the glomerular layer, the external plexiform layer, the mitral cell layer, and the internal plexiform layer. This divergence in the numbers of NC cells was especially patent in central rostrocaudal levels. The NC-containing neurons exhibiting sexual divergence were identified as both juxtaglomerular and short-axon cells. This is the first description of sexual dimorphism regarding neurons belonging to the mouse main OB. According to their distribution in the OB, neurocalcin-immunoreactive interneurons could reflect a sexually dimorphic regulation of specific odorants.
Subject(s)
Neurocalcin/analysis , Neurons/chemistry , Olfactory Bulb/chemistry , Animals , Cell Count , Female , Immunohistochemistry , Interneurons/chemistry , Interneurons/cytology , Male , Mice , Mice, Inbred Strains , Neurons/cytology , Olfactory Bulb/cytology , Sex FactorsABSTRACT
Postnatally, the Purkinje cell degeneration mutant mice lose the main projecting neurons of the main olfactory bulb (OB): mitral cells (MC). In adult animals, progenitor cells from the rostral migratory stream (RMS) differentiate into bulbar interneurons that modulate MC activity. In the present work, we studied changes in proliferation, tangential migration, radial migration patterns, and the survival of these newly generated neurons in this neurodegeneration animal model. The animals were injected with bromodeoxyuridine 2 weeks or 2 months before killing in order to label neuroblast incorporation into the OB and to analyze the survival of these cells after differentiation, respectively. Both the organization and cellular composition of the RMS and the differentiation of the newly generated neurons in the OB were studied using specific markers of glial cells, neuroblasts, and mature neurons. No changes were observed in the cell proliferation rate nor in their tangential migration through the RMS, indicating that migrating neuroblasts are only weakly responsive to the alteration in their target region, the OB. However, the absence of MC does elicit differences in the final destination of the newly generated interneurons. Moreover, the loss of MC also produces changes in the survival of the newly generated interneurons, in accordance with the dramatic decrease in the number of synaptic targets available.
Subject(s)
Cell Differentiation/physiology , Cell Movement/physiology , Cell Proliferation , Neurons/physiology , Olfactory Bulb/physiology , Stem Cells/physiology , Animals , Biomarkers/analysis , Biomarkers/metabolism , Bromodeoxyuridine , Cell Adhesion Molecules, Neuronal/metabolism , Cell Survival/physiology , Disease Models, Animal , Extracellular Matrix Proteins/metabolism , In Situ Nick-End Labeling , Interneurons/cytology , Interneurons/physiology , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Nerve Degeneration/metabolism , Nerve Degeneration/physiopathology , Nerve Tissue Proteins/metabolism , Neuroglia/cytology , Neuroglia/physiology , Neurons/cytology , Olfactory Bulb/cytology , Reelin Protein , Serine Endopeptidases/metabolism , Stem Cells/cytologyABSTRACT
The dopaminergic system plays important roles in the modulation of olfactory transmission. The present study examines the distribution of dopaminergic cells and the content of dopamine (DA) and its metabolites in control and deprived olfactory bulbs (OB), focusing on the differences between sexes. The content of DA and of its metabolites, dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), were measured by HPLC. The morphology and distribution of dopaminergic neurons were studied using tyrosine hydroxylase (TH) immunohistochemistry. Cells were typified with TH-parvalbumin, TH-cholecystokinin or TH-neurocalcin double-immunofluorescence assays. Biochemical analyses revealed sex differences in the content of DA and of its metabolites. In normal conditions, the OBs of male rats had higher concentrations of DA, DOPAC and HVA than the OBs of females. The immunohistochemical data pointed to sex differences in the number of TH-immunopositive cells (higher in male than in female rats). Colocalization analyses revealed that dopaminergic cells constitute a different cell subpopulation from those labelled after parvalbumin, cholecystokinin or neurocalcin immunostaining. Unilateral olfactory deprivation caused dramatic alterations in the dopaminergic system. The DA content and the density of dopaminergic cells decreased, the contents of DA and DOPAC as well as TH immunoreactivity were similar in deprived males and females and, finally, the metabolite/neurotransmitter ratio increased. Our results show that the dopaminergic modulation of olfactory transmission seems to differ between males and females and that it is regulated by peripheral olfactory activity. A possible role of the dopaminergic system in the sexually different olfactory sensitivity, discrimination and memory is discussed.
Subject(s)
Catechols/metabolism , Functional Laterality/physiology , Olfactory Bulb/metabolism , Sensory Deprivation/physiology , Sex Characteristics , 3,4-Dihydroxyphenylacetic Acid/metabolism , Animals , Animals, Newborn , Chromatography, High Pressure Liquid/methods , Dopamine/metabolism , Female , Homovanillic Acid/metabolism , Male , Nerve Tissue Proteins/metabolism , Pregnancy , Rats , Tyrosine 3-Monooxygenase/metabolismABSTRACT
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