Human voltage-gated Na+ and K+ channel properties underlie sustained fast AP signaling

  • René Wilbers
  • , Verjinia D Metodieva
  • , Sarah Duverdin
  • , Djai B Heyer
  • , Anna A Galakhova
  • , Eline J Mertens
  • , Tamara D Versluis
  • , Johannes C Baayen
  • , Sander Idema
  • , David P Noske
  • , Niels Verburg
  • , Ronald B Willemse
  • , Philip C de Witt Hamer
  • , Maarten H P Kole
  • , Christiaan P J de Kock
  • , Huibert D Mansvelder
  • , Natalia A Goriounova*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Human cortical pyramidal neurons are large, have extensive dendritic trees, and yet have unexpectedly fast input-output properties: Rapid subthreshold synaptic membrane potential changes are reliably encoded in timing of action potentials (APs). Here, we tested whether biophysical properties of voltage-gated sodium (Na+) and potassium (K+) currents in human pyramidal neurons can explain their fast input-output properties. Human Na+ and K+ currents exhibited more depolarized voltage dependence, slower inactivation, and faster recovery from inactivation compared with their mouse counterparts. Computational modeling showed that despite lower Na+ channel densities in human neurons, the biophysical properties of Na+ channels resulted in higher channel availability and contributed to fast AP kinetics stability. Last, human Na+ channel properties also resulted in a larger dynamic range for encoding of subthreshold membrane potential changes. Thus, biophysical adaptations of voltage-gated Na+ and K+ channels enable fast input-output properties of large human pyramidal neurons.

Original languageEnglish
Article numbereade3300
Number of pages14
JournalScience advances
Volume9
Issue number41
DOIs
Publication statusPublished - 13 Oct 2023

Keywords

  • Action Potentials/physiology
  • Animals
  • Humans
  • Membrane Potentials/physiology
  • Mice
  • Neurons/physiology
  • Pyramidal Cells/physiology
  • Sodium

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