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Up- and down-regulation of the mechano-gated K2P channel TREK-1 by PIP2 and other membrane phospholipids
Chemin, J.; Patel, A.J.; Duprat, F.; Sachs, F.; Lazdunski, M.; Honoré, E. (2007). Up- and down-regulation of the mechano-gated K2P channel TREK-1 by PIP2 and other membrane phospholipids. Pflügers Arch. Eur. J. Physiol. 455(1): 97-103.
In: Pflügers Archiv - European Journal of Physiology. Springer: Berlin. ISSN 0031-6768, more
Peer reviewed article  

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  • Chemin, J.
  • Patel, A.J.
  • Duprat, F.
  • Sachs, F.
  • Lazdunski, M.
  • Honoré, E., more

    TREK-1 is an unconventional K+ channel that is activated by both physical and chemical stimuli. In this study, we show that the inner leaflet membrane phospholipids, including PIP2, exert a mixed stimulatory and inhibitory effect on TREK-1. Intra-cellular phospholipids inhibit basal channel activity and activation by membrane stretch, intra-cellular acidosis and arachidonic acid. However, binding of endogenous negative inner leaflet phospholipids with poly-lysine reduces inhibition and reveals channel stimulation by exogenous intra-cellular phospholipids. A similar effect is observed with PI, PE, PS and PA, unlike DG, demonstrating that the phosphate at position 3 is required although the global charge of the molecule is not critical. Inhibition depends on the distal C-terminal domain that conditions channel mechano-sensitivity, but is independent of the positively charged PIP2 stimulatory site in the proximal C-terminal domain. This is, to our knowledge, the first report of an ion channel dually regulated by membrane phospholipids.

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