Abstract:The perception and discriminating of odors are sensory activities that are an integral part of our daily life. The first brain region where odors are processed is the olfactory bulb (OB). Among the different cell populations that make up this brain area, interneurons play an essential role in this sensory activity. Moreover, probably because of their activity, they represent an exception compared to other parts of the brain, since OB interneurons are continuously generated in the postnatal and adult period. In… Show more
“…Given that dopaminergic cells process odor cues, the reduction of dopamine neurons, receptors or transporters decreases the capability to discriminate odors ( Taylor et al, 2009 ; Paß et al, 2020 ). On the other hand, calretinin interneurons are responsible for inhibiting noisy excitatory signals that reach mitral/tufted cells ( Capsoni et al, 2021 ). Interestingly, a pool of calretinin periglomerular cells remains in an immature stage for a long time, and it has been proposed that these cells could supply glomerular networks dependent on specific sensory experiences ( Benito et al, 2018 ).…”
“…Given that dopaminergic cells process odor cues, the reduction of dopamine neurons, receptors or transporters decreases the capability to discriminate odors ( Taylor et al, 2009 ; Paß et al, 2020 ). On the other hand, calretinin interneurons are responsible for inhibiting noisy excitatory signals that reach mitral/tufted cells ( Capsoni et al, 2021 ). Interestingly, a pool of calretinin periglomerular cells remains in an immature stage for a long time, and it has been proposed that these cells could supply glomerular networks dependent on specific sensory experiences ( Benito et al, 2018 ).…”
“…These cells are mature neurons with multiple processes. A GFP-labeled cell in the deep layer of the OB expressed CR, which is characteristic of the OB interneuron subtype (Capsoni et al, 2021). OB interneurons are heterogeneous and have multiple origins (Qin et al, 2017).…”
Section: Novel Destination Of Op-derived Neurons In the Brainmentioning
Cell migration from the olfactory placode (OP) is a well-known phenomenon wherein various cell types, such as gonadotropin-releasing hormone (GnRH)producing neurons, migrate toward the telencephalon (TEL) during early embryonic development. However, the spatial relationship between early migratory cells and the forebrain is unclear. We examined the early development of whole-mount chick embryos to observe the three-dimensional spatial relationship among OP-derived migratory neurons, olfactory nerve (ON), and TEL. Migratory neurons that express highly polysialylated neural cell adhesion molecule (PSA-NCAM) emerge from the OP and spread over a relatively wide TEL area at the Hamburger and Hamilton (HH) stage 17. Most migratory neurons form a cellular cord between the olfactory pit and rostral TEL within HH18-20. The earliest axons from the olfactory epithelium (OE) were detected along this neuronal cord using DiI-labeling at HH21. Furthermore, a few PSA-NCAM-positive neurons were dispersed around the cellular cord and over the lateral TEL at HH18. A long cellular cord branch extending to the lateral TEL was transiently observed within HH18-24. These results suggest a novel migratory route of OP-derived neurons during the early developmental stages. Following GFP vector introduction into the OP of HH13-15 embryos, labeled neurons were detected around and within the lateral TEL at HH23 and HH27. At HH36, labeled cells were observed in the rostral-lateral TEL, including the olfactory bulb (OB) region. GFP-labeled and calretinin-positive neurons were detected in the OB, suggesting that early OP-derived neurons enter the forebrain and function as interneurons in the OB.
“…In particular, the outermost portion of the adult OB, termed the glomerular layer (GL), is characterized by the presence of dopaminergic (DAergic) interneurons [ 1 , 2 , 3 ]. These cells play a key role in odor processing [ 4 , 5 , 6 ]. They are responsible for significant activity-dependent plasticity, controlling the release of dopamine [ 7 , 8 , 9 , 10 ], which will lead to an adaptation of the olfactory bulbar network to external conditions.…”
Section: Introductionmentioning
confidence: 99%
“…They control the local gain of transmitter release from the terminals of the olfactory sensory neurons [ 11 , 12 , 13 ] and determine the inhibition of lateral glomerular output [ 14 ]. For a complete anatomical, functional and electrophysiological description of these neurons, the reader may refer to the reviews by Pignatelli et al [ 2 , 4 , 15 , 16 , 17 ].…”
The olfactory bulb (OB) is one of two regions of the mammalian brain which undergo continuous neuronal replacement during adulthood. A significant fraction of the cells added in adulthood to the bulbar circuitry is constituted by dopaminergic (DA) neurons. We took advantage of a peculiar property of dopaminergic neurons in transgenic mice expressing eGFP under the tyrosine hydroxylase (TH) promoter: while DA neurons located in the glomerular layer (GL) display full electrophysiological maturation, eGFP+ cells in the mitral layer (ML) show characteristics of immature cells. In addition, they also display a lower fluorescence intensity, possibly reflecting different degrees of maturation. To investigate whether this difference in maturation might be confirmed at the gene expression level, we used a fluorescence-activated cell sorting technique on enzymatically dissociated cells of the OB. The cells were divided into two groups based on their level of fluorescence, possibly corresponding to immature ML cells and fully mature DA neurons from the GL. Semiquantitative real-time PCR was performed to detect the level of expression of genes linked to the degree of maturation of DA neurons. We showed that indeed the cells expressing low eGFP fluorescence are immature neurons. Our method can be further used to explore the differences between these two groups of DA neurons.
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