A quantized mechanism for activation of pannexin channels

Nat Commun. 2017 Jan 30:8:14324. doi: 10.1038/ncomms14324.

Abstract

Pannexin 1 (PANX1) subunits form oligomeric plasma membrane channels that mediate nucleotide release for purinergic signalling, which is involved in diverse physiological processes such as apoptosis, inflammation, blood pressure regulation, and cancer progression and metastasis. Here we explore the mechanistic basis for PANX1 activation by using wild type and engineered concatemeric channels. We find that PANX1 activation involves sequential stepwise sojourns through multiple discrete open states, each with unique channel gating and conductance properties that reflect contributions of the individual subunits of the hexamer. Progressive PANX1 channel opening is directly linked to permeation of ions and large molecules (ATP and fluorescent dyes) and occurs during both irreversible (caspase cleavage-mediated) and reversible (α1 adrenoceptor-mediated) forms of channel activation. This unique, quantized activation process enables fine tuning of PANX1 channel activity and may be a generalized regulatory mechanism for other related multimeric channels.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Amino Acid Chloromethyl Ketones / pharmacology
  • Carbenoxolone / pharmacology
  • Caspase Inhibitors / pharmacology
  • Caspases / metabolism
  • Cell Membrane / metabolism*
  • Cell Membrane / ultrastructure
  • Cell Membrane Permeability / drug effects
  • Cell Membrane Permeability / physiology*
  • Connexins / antagonists & inhibitors
  • Connexins / metabolism*
  • Connexins / ultrastructure
  • Fluorescent Dyes / pharmacokinetics
  • Fluoroquinolones / pharmacology
  • HEK293 Cells
  • Humans
  • Ions / metabolism
  • Jurkat Cells
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Microscopy, Electron
  • Naphthyridines / pharmacology
  • Nerve Tissue Proteins / antagonists & inhibitors
  • Nerve Tissue Proteins / metabolism*
  • Nerve Tissue Proteins / ultrastructure
  • Patch-Clamp Techniques
  • Protein Multimerization / physiology*
  • Quinolines / pharmacology
  • Receptors, Adrenergic, alpha-1 / metabolism

Substances

  • Amino Acid Chloromethyl Ketones
  • Caspase Inhibitors
  • Connexins
  • Fluorescent Dyes
  • Fluoroquinolones
  • Ions
  • Naphthyridines
  • Nerve Tissue Proteins
  • PANX1 protein, human
  • Quinolines
  • Receptors, Adrenergic, alpha-1
  • quinoline-val-asp(OMe)-CH2-OPH
  • Adenosine Triphosphate
  • trovafloxacin
  • Caspases
  • Carbenoxolone