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A New TASK for Dipeptidyl Peptidase-like Protein 6

Overview of attention for article published in PLOS ONE, April 2013
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Title
A New TASK for Dipeptidyl Peptidase-like Protein 6
Published in
PLOS ONE, April 2013
DOI 10.1371/journal.pone.0060831
Pubmed ID
Authors

Brian M. Nadin, Paul J. Pfaffinger

Abstract

Dipeptidyl Peptidase-like Protein 6 (DPP6) is widely expressed in the brain where it co-assembles with Kv4 channels and KChIP auxiliary subunits to regulate the amplitude and functional properties of the somatodendritic A-current, ISA. Here we show that in cerebellar granule (CG) cells DPP6 also regulates resting membrane potential and input resistance by increasing the amplitude of the IK(SO) resting membrane current. Pharmacological analysis shows that DPP6 acts through the control of a channel with properties matching the K2P channel TASK-3. Heterologous expression and co-immunoprecipitation shows that DPP6 co-expression with TASK-3 results in the formation of a protein complex that enhances resting membrane potassium conductance. The co-regulation of resting and voltage-gated channels by DPP6 produces coordinate shifts in resting membrane potential and A-current gating that optimize the sensitivity of ISA inactivation gating to subthreshold fluctuations in resting membrane potential.

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The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 7%
Unknown 13 93%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 29%
Professor > Associate Professor 3 21%
Student > Master 2 14%
Student > Bachelor 2 14%
Other 1 7%
Other 2 14%
Readers by discipline Count As %
Agricultural and Biological Sciences 6 43%
Medicine and Dentistry 5 36%
Neuroscience 2 14%
Biochemistry, Genetics and Molecular Biology 1 7%