Guanosine modulates K+ membrane currents in SH-SY5Y cells: involvement of adenosine receptors

Pflugers Arch. 2022 Nov;474(11):1133-1145. doi: 10.1007/s00424-022-02741-4. Epub 2022 Sep 1.

Abstract

Guanosine (GUO), widely considered a key signaling mediator, is implicated in the regulation of several cellular processes. While its interaction with neural membranes has been described, GUO still is an orphan neuromodulator. It has been postulated that GUO may eventually interact with potassium channels and adenosine (ADO) receptors (ARs), both particularly important for the control of cellular excitability. Accordingly, here, we investigated the effects of GUO on the bioelectric activity of human neuroblastoma SH-SY5Y cells by whole-cell patch-clamp recordings. We first explored the contribution of voltage-dependent K+ channels and, besides this, the role of ARs in the regulation of GUO-dependent cellular electrophysiology. Our data support that GUO is able to specifically modulate K+-dependent outward currents over cell membranes. Importantly, administering ADO along with GUO potentiates its effects. Overall, these results suggested that K+ outward membrane channels may be targeted by GUO with an implication of ADO receptors in SH-SY5Y cells, but also support the hypothesis of a functional interaction of the two ligands. The present research runs through the leitmotif of the deorphanization of GUO, adding insight on the interplay with adenosinergic signaling and suggesting GUO as a powerful modulator of SH-SY5Y excitability.

Keywords: Cellular excitability; Electrophysiology; Patch-clamp; Potassium channels; Purines; SH-SY5Y cells.

MeSH terms

  • Adenosine
  • Guanosine* / pharmacology
  • Humans
  • Ligands
  • Neuroblastoma* / metabolism
  • Potassium Channels
  • Receptors, Purinergic P1 / metabolism

Substances

  • Ligands
  • Potassium Channels
  • Receptors, Purinergic P1
  • Guanosine
  • Adenosine