Journal
JOURNAL OF COMPARATIVE NEUROLOGY
Volume 518, Issue 21, Pages 4362-4374Publisher
WILEY
DOI: 10.1002/cne.22461
Keywords
Cav3.1; thalamus; electron microscopy; preembedding immunogold labeling; 3D reconstruction; dendrite
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Funding
- SORST
- CREST
- Japan Science and Technology Agency (JST)
- Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) [20019031, 18022043]
- Grants-in-Aid for Scientific Research [20019031, 18022043] Funding Source: KAKEN
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T-type calcium channels play a pivotal role in regulating neural membrane excitability in the nervous system. However, the precise subcellular distributions of T-type channel subunits and their implication for membrane excitability are not well understood. Here we investigated the subcellular distribution of the alpha 1G subunit of the calcium channel which is expressed highly in the mouse dorsal lateral geniculate nucleus (dLGN). Light microscopic analysis demonstrated that dLGN exhibits intense immunoperoxidase reactivity for the alpha 1G subunit. Electron microscopic observation showed that the labeling was present in both the relay cells and interneurons and was found in the somatodendritic, but not axonal, domains of these cells. Most of the immunogold particles for the alpha 1G subunit were either associated with the plasma membrane or the intracellular membranes. Reconstruction analysis of serial electron microscopic images revealed that the intensity of the intracellular labeling exhibited a gradient such that the labeling density was higher in the proximal dendrite and progressively decreased towards the distal dendrite. In contrast, the plasma membrane-associated particles were distributed with a uniform density over the somatodendritic surface of dLGN cells. The labeling density in the relay cell plasma membrane was about 3-fold higher than that of the interneurons. These results provide ultrastructural evidence for cell-type-specific expression levels and for uniform expression density of the alpha 1G subunit over the plasma membrane of dLGN cells. J. Comp. Neurol. 518: 4362-4374, 2010. (C) 2010 Wiley-Liss, Inc.
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