Abstract

ADP and other nucleotides control ion currents in the nervous system via various P2Y receptors. In this respect, Cav2 and Kv7 channels have been investigated most frequently. The fine tuning of neuronal ion channel gating via G protein coupled receptors frequently relies on the formation of higher order protein complexes that are organized by scaffolding proteins and harbor receptors and channels together with interposed signaling components. However, ion channel complexes containing P2Y receptors have not been described. Therefore, the regulation of Cav2.2 and Kv7.2/7.3 channels via P2Y1 and P2Y12 receptors and the coordination of these ion channels and receptors in the plasma membranes of tsA 201 cells have been investigated here. ADP inhibited currents through Cav2.2 channels via both P2Y1 and P2Y12 receptors with phospholipase C and pertussis toxin-sensitive G proteins being involved, respectively. The nucleotide controlled the gating of Kv7 channels only via P2Y1 and phospholipase C. In fluorescence energy transfer assays using conventional as well as total internal reflection (TIRF) microscopy, both P2Y1 and P2Y12 receptors were found juxtaposed to Cav2.2 channels, but only P2Y1, and not P2Y12, was in close proximity to Kv7 channels. Using fluorescence recovery after photobleaching in TIRF microscopy, evidence for a physical interaction was obtained for the pair P2Y12/Cav2.2, but not for any other receptor/channel combination. These results reveal a membrane juxtaposition of P2Y receptors and ion channels in parallel with the control of neuronal ion currents by ADP. This juxtaposition may even result in apparent physical interactions between receptors and channels.

Highlights

  • P2Y receptors are a group of G protein coupled receptors (GPCRs) that are expressed in almost every tissue of the vertebrate body, including the nervous system [1]

  • To investigate whether the modulation of neuronal ion currents by ADP is paralleled by a certain spatial arrangement of P2Y receptors and ion channels, P2Y1 and P2Y12 receptors, respectively, were expressed in tsA 201 cells together with either Kv7.2/Kv7.3 heteromers or Cav2.2 channels

  • Using fluorescently labeled receptors and calculations of Normalized FRET (NFRET) values, we have shown that P2Y1 and P2Y12 receptors can form homomers and

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Summary

Introduction

P2Y receptors are a group of G protein coupled receptors (GPCRs) that are expressed in almost every tissue of the vertebrate body, including the nervous system [1]. They are activated by nucleotides such as ATP, ADP, UTP, or UDP. Eight different subtypes are known which are preferentially linked to either Gαq (P2Y1, P2Y2, P2Y4, P2Y6, P2Y11) or Gαi (P2Y12, P2Y13, and P2Y14) subunits of heterotrimeric G proteins [2] Many of these receptors have been shown to regulate the functions of neuronal ion channels [3]. P2Y12 receptors are involved in the inhibition of calcium channels [15, 16] and K2P channels [5] by ADP

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