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Differential targeting and functional specialization of sodium channels in cultured cerebellar granule cells
Author(s) -
Osorio Nancy,
Alcaraz Gisèle,
Padilla Françoise,
Couraud François,
Delmas Patrick,
Crest Marcel
Publication year - 2005
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2005.097022
Subject(s) - sodium channel , microbiology and biotechnology , axon , ion channel , biology , nav1 , somatic cell , in vitro , neuroscience , membrane potential , chemistry , biophysics , sodium , biochemistry , gene , receptor , organic chemistry
The ion channel dynamics that underlie the complex firing patterns of cerebellar granule (CG) cells are still largely unknown. Here, we have characterized the subcellular localization and functional properties of Na + channels that regulate the excitability of CG cells in culture. As evidenced by RT‐PCR and immunocytochemical analysis, morphologically differentiated CG cells expressed Nav1.2 and Nav1.6, though both subunits appeared to be differentially regulated. Nav1.2 was localized at most axon initial segments (AIS) of CG cells from 8 days in vitro DIV 8 to DIV 15. At DIV 8, Nav1.6 was found uniformly throughout somata, dendrites and axons with occasional clustering in a subset of AIS. Accumulation of Nav1.6 at most AIS was evident by DIV 13–14, suggesting it is developmentally regulated at AIS. The specific contribution of these differentially distributed Na + channels has been assessed using a combination of methods that allowed discrimination between functionally compartmentalized Na + currents. In agreement with immunolocalization, we found that fast activating–fully inactivating Na + currents predominate at the AIS membrane and in the somatic plasma membrane.