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Publication : Sodium channel cluster, betaIV-spectrin and ankyrinG positive "hot spots" on dendritic segments of parvalbumin-containing neurons and some other neurons in the mouse and rat main olfactory bulbs.

First Author  Kosaka T Year  2008
Journal  Neurosci Res Volume  62
Issue  3 Pages  176-86
PubMed ID  18786578 Mgi Jnum  J:141253
Mgi Id  MGI:3817818 Doi  10.1016/j.neures.2008.08.002
Citation  Kosaka T, et al. (2008) Sodium channel cluster, betaIV-spectrin and ankyrinG positive 'hot spots' on dendritic segments of parvalbumin-containing neurons and some other neurons in the mouse and rat main olfactory bulbs. Neurosci Res 62(3):176-86
abstractText  Axon initial segments (AISs) and nodes of Ranvier are considered as the sites for spike generation, which are highly enriched in sodium channels and some cytoskeletal molecules such as ankyrinG, betaIV-spectrin. Previously, we showed that most parvalbumin positive cells in the external plexiform layer (EPL) of the mouse main olfactory bulb (MOB) were anaxonic but displayed some patch-like betaIV-spectrin and sodium channel cluster positive segments on their dendrites. In this study we further characterized those particular dendritic segments. AnkyrinG was also located there, whereas phospho-IkappaBalpha was not. Electron-microscopically those dendritic segments displayed the membrane undercoating characteristic to the AISs and nodes of Ranvier, further confirming their resemblance to the spike generation sites, 'hot spots'. Three-dimensional analysis revealed that each parvalbumin positive EPL neuron had 2-7 hot spots, 3-28mum in length and located 7-50mum from the somata. Similar 'hot spots' were also encountered on a few calretinin positive granule cells and nitric oxide synthase positive periglomerular cells in the mouse MOB. In addition parvalbumin positive EPL cells in the rat MOB displayed similar multiple dendritic 'hot spots'. Our study suggested that these morphologically identified dendritic 'hot spots' might correspond to dendritic spike generation sites of those neurons.
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