DPP10 modulates Kv4-mediated A-type potassium channels

J Biol Chem. 2005 May 13;280(19):18853-61. doi: 10.1074/jbc.M410613200. Epub 2005 Jan 25.


A new member of a family of proteins characterized by structural similarity to dipeptidyl peptidase (DPP) IV known as DPP10 was recently identified and linked to asthma susceptibility; however, the cellular functions of DPP10 are thus far unknown. DPP10 is highly homologous to subfamily member DPPX, which we previously reported as a modulator of Kv4-mediated A-type potassium channels (Nadal, M. S., Ozaita, A., Amarillo, Y., Vega-Saenz de Miera, E., Ma, Y., Mo, W., Goldberg, E. M., Misumi, Y., Ikehara, Y., Neubert, T. A., and Rudy, B. (2003) Neuron. 37, 449-461). We studied the ability of DPP10 protein to modulate the properties of Kv4.2 channels in heterologous expression systems. We found DPP10 activity to be nearly identical to DPPX activity and significantly different from DPPIV activity. DPPX and DPP10 facilitated Kv4.2 protein trafficking to the cell membrane, increased A-type current magnitude, and modified the voltage dependence and kinetic properties of the current such that they resembled the properties of A-type currents recorded in neurons in the central nervous system. Using in situ hybridization, we found DPP10 to be prominently expressed in brain neuronal populations that also express Kv4 subunits. Furthermore, DPP10 was detected in immunoprecipitated Kv4.2 channel complexes from rat brain membranes, confirming the association of DPP10 proteins with native Kv4.2 channels. These experiments suggest that DPP10 contributes to the molecular composition of A-type currents in the central nervous system. To dissect the structural determinants of these integral accessory proteins, we constructed chimeras of DPPX, DPP10, and DPPIV lacking the extracellular domain. Chimeras of DPPX and DPP10, but not DPPIV, were able to modulate the properties of Kv4.2 channels, highlighting the importance of the intracellular and transmembrane domains in this activity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Biotinylation
  • Blotting, Northern
  • Brain / metabolism
  • CHO Cells
  • Cell Membrane / metabolism
  • Central Nervous System / metabolism
  • Cricetinae
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / metabolism
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases / physiology*
  • Electrophysiology
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Immunoprecipitation
  • In Situ Hybridization
  • Kinetics
  • Mass Spectrometry
  • Mice
  • Mice, Inbred C57BL
  • Models, Molecular
  • Molecular Sequence Data
  • Nerve Tissue Proteins / metabolism
  • Nerve Tissue Proteins / physiology
  • Neurons / metabolism
  • Peptides / chemistry
  • Potassium Channels / metabolism
  • Potassium Channels / physiology
  • Potassium Channels, Voltage-Gated / metabolism*
  • Protein Conformation
  • Protein Structure, Tertiary
  • RNA / chemistry
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Fusion Proteins / chemistry
  • Sequence Homology, Amino Acid
  • Shal Potassium Channels
  • Time Factors
  • Transfection


  • Nerve Tissue Proteins
  • Peptides
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Recombinant Fusion Proteins
  • Shal Potassium Channels
  • RNA
  • DPP10 protein, human
  • DPP10 protein, mouse
  • DPP6 protein, rat
  • Dipeptidyl-Peptidases and Tripeptidyl-Peptidases