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DPP10 splice variants are localized in distinct neuronal populations and act to differentially regulate the inactivation properties of Kv4-based ion channels

Authors
Journal
Molecular and Cellular Neuroscience
1044-7431
Publisher
Elsevier
Publication Date
Volume
35
Issue
4
Identifiers
DOI: 10.1016/j.mcn.2007.03.008
Keywords
  • Somatodendritric A-Type Current (Isa)
  • Kv4 Potassium Channel
  • Kv Channel-Interacting Protein (Kchip)
  • Dipeptidyl Aminopeptidase-Like Protein (Dpl)
  • Inactivation Gating
Disciplines
  • Biology

Abstract

Abstract Dipeptidyl peptidase-like proteins (DPLs) and Kv-channel-interacting proteins (KChIPs) join Kv4 pore-forming subunits to form multi-protein complexes that underlie subthreshold A-type currents (I SA) in neuronal somatodendritic compartments. Here, we characterize the functional effects and brain distributions of N-terminal variants belonging to the DPL dipeptidyl peptidase 10 (DPP10). In the Kv4.2 + KChIP3 + DPP10 channel complex, all DPP10 variants accelerate channel gating kinetics; however, the splice variant DPP10a produces uniquely fast inactivation kinetics that accelerates with increasing depolarization. This DPP10a-specific inactivation dominates in co-expression studies with KChIP4a and other DPP10 isoforms. Real-time qRT-PCR and in situ hybridization analyses reveal differential expression of DPP10 variants in rat brain. DPP10a transcripts are prominently expressed in the cortex, whereas DPP10c and DPP10d mRNAs exhibit more diffuse distributions. Our results suggest that DPP10a underlies rapid inactivation of cortical I SA, and the regulation of isoform expression may contribute to the variable inactivation properties of I SA across different brain regions.

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