G protein‐activated K+ channels: a reporter for rapid activation of G proteins by lysophosphatidic acid in Xenopus oocytes
Irit Itzhaki Van‐Ham, Sagit Peleg, Nathan Dascal, Hagit Shapira, Yoram Oron
Abstract
Irit Itzhaki Van‐Ham, Sagit Peleg, Nathan Dascal, Hagit Shapira, Yoram Oron
Abstract
Threshold concentrations of lysophosphatidic acid (LPA) or acetylcholine (ACh) induce pertussis toxin (PTX)-sensitive rapid desensitization of responses to LPA in Xenopus oocytes. To demonstrate that threshold [LPA] rapidly activates Gi/o proteins, we used the G protein-activated K+ channel (GIRK) as a reporter. Low [LPA] induced IK+ in <3 s of the agonist addition with little or no activation of chloride current. Depletion of Galphao/Galphao1 each decreased the LPA-induced IK+ by approximately 40-50%, while PTX completely abolished it. This is the first direct evidence showing the activation of GIRK by LPA, and the involvement of G proteins of the Go family in rapid desensitization of LPA responses.
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Threshold concentrations of lysophosphatidic acid (LPA) or acetylcholine (ACh) induce pertussis toxin (PTX)-sensitive rapid desensitization of responses to LPA in Xenopus oocytes. To demonstrate that threshold [LPA] rapidly activates Gi/o proteins, we used the G protein-activated K+ channel (GIRK) as a reporter. Low [LPA] induced IK+ in <3 s of the agonist addition with little or no activation of chloride current. Depletion of Galphao/Galphao1 each decreased the LPA-induced IK+ by approximately 40-50%, while PTX completely abolished it. This is the first direct evidence showing the activation of GIRK by LPA, and the involvement of G proteins of the Go family in rapid desensitization of LPA responses.
Key concepts: Lysophosphatidic acid, Pertussis toxin, G protein-coupled inwardly-rectifying potassium channel, Xenopus, G protein, Desensitization (medicine), Chemistry, Chloride channel