4.6 Article

Effects of unsaturated fatty acids on the kinetics of voltage-gated proton channels heterologously expressed in cultured cells

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 594, 期 3, 页码 595-610

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WILEY-BLACKWELL
DOI: 10.1113/JP271274

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资金

  1. Japan Society for the Promotion of Science (KAKENHI) [25253016, 15H05901, 15K18516]
  2. Japan Society for the Promotion of Science for Young Scientists [10J01585]
  3. Grants-in-Aid for Scientific Research [15K18516, 10J01585, 26111712, 25253016, 15H05901, 15H05897] Funding Source: KAKEN

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Unsaturated fatty acids are key components of the biological membranes of all cells, and precursors of mediators for cell signalling. Arachidonic acid (AA) is an unsaturated fatty acid known to modulate the activities of various ion channels, including the voltage-gated proton (Hv) channel, which supports the rapid production of reactive oxygen species (ROS) in phagocytes through regulation of pH and membrane potential. However, the molecular mechanisms and physiological functions of the effects of AA on Hv channels remain unclear. In the present study, we report an electrophysiological analysis of the effects of AA on the mouse Hv channel (mHv1) heterologously expressed in HEK293T cells. Application of AA to excised inside-out patch membranes rapidly induced a robust increase in the amplitude of the proton current through mHv1. The current increase was accompanied by accelerated activation kinetics and a small leftward shift of the current-voltage relationship. In monomeric channels lacking the coiled-coil region of the channel protein, the shift in the current-voltage relationship was diminished but activation and deactivation remained accelerated. Studies with several AA derivatives showed that double bonds and hydrophilic head groups are essential for the effect of AA, although charge was not important. The application of phospholipase A(2) (PLA(2)), which generates AA from cell membrane phospholipids, stimulated mHv1 activity to a similar extent as direct application of approximate to 20m AA, suggesting that endogenous AA may regulate Hv channel activity.

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