Cationic control of panx1 channel function

Junjie Wang, David George Jackson, Gerhard Dahl

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


The sequence and predicted membrane topology of pannexin1 (Panx1) places it in the family of gap junction proteins. However, rather than forming gap junction channels, Panx1 forms channels in the nonjunctional membrane. Panx1 operates in two distinct open states, depending on the mode of stimulation. The exclusively voltage-gated channel has a small conductance (<100 pS) and is highly selective for the flux of chloride ions. The Panx1 channel activated by various physiological stimuli or by increased concentrations of extracellular potassium ions has a large conductance (~500 pS, however, with multiple, long-lasting subconductance states) and is nonselectively permeable to small molecules, including ATP. To test whether the two open conformations also differ pharmacologically, the effects of di-and trivalent cations on the two Panx1 channel conformations were investigated. The rationale for this venture was that, under certain experimental conditions, ATP release from cells can be inhibited by multivalent cations, yet the literature indicates that the ATP release channel Panx1 is not affected by these ions. Consistent with previous reports, the Panx1 channel was not activated by removal of extracellular Ca2+ and the currents through the voltage-activated channel were not altered by Ca2+,Zn2+, Ba2+, or Gd3+. In contrast, the Panx1 channel activated to the large channel conformation by extracellular K+, osmotic stress, or low oxygen was inhibited by the multivalent cations in a dose-dependent way. Thus, monovalent cations activated the Panx1 channel from the closed state to the “large” conformation, while di-and trivalent cations exclusively inhibited this large channel conformation.

Original languageEnglish (US)
Pages (from-to)C279-C289
JournalAmerican Journal of Physiology - Cell Physiology
Issue number3
StatePublished - Sep 2018


  • Calcium
  • Gadolinium
  • Pannexin
  • Potassium
  • Voltage

ASJC Scopus subject areas

  • Physiology
  • Cell Biology


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