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


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2022-09-01

AUTHORS

Giuditta Gambino, Giuseppe Giglia, Daniele Gallo, Miriana Scordino, Costanza Giardina, Mariachiara Zuccarini, Patrizia Di Iorio, Patricia Giuliani, Francisco Ciruela, Giuseppe Ferraro, Giuseppa Mudò, Pierangelo Sardo, Valentina Di Liberto

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. More... »

PAGES

1133-1145

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00424-022-02741-4

DOI

http://dx.doi.org/10.1007/s00424-022-02741-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1150678110

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/36048287


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