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Regulation of inositol 1,4,5-trisphosphate-induced Ca2+ release from the endoplasmic reticulum by AMP-activated kinase modulators

AuthorsArias-del-Val, Jessica; Santo-Domingo, Jaime; García-Casas, Paloma; Alvarez-Illera, Pilar; Núñez Galindo, Antonio; Wiederkehr, Andreas; Fonteriz, Rosalba I. CSIC ORCID; Montero, Mayte CSIC ORCID CVN; Álvarez, Javier
Inositol-1,4,5-trisphosphate receptor
Ca2+ signaling
Endoplasmic reticulum
Issue Date2019
CitationCell Calcium 77: 68-76 (2019)
AbstractThe 5' AMP-activated protein kinase (AMPK) is a nutrient-sensitive kinase that plays a key role in the control of cellular energy metabolism. We have explored here the relationship between AMPK and Ca2+ signaling by looking at the effect of an AMPK activator (A769662) and an AMPK inhibitor (dorsomorphin) on histamine-induced Ca2+-release from the endoplasmic reticulum (ER) in HeLa cells. Our data show that incubation with A769662 (EC50 = 29 μM) inhibited histamine-induced Ca2+-release from the ER in intact cells, as well as inositol-1,4,5-trisphosphate (IP3)-induced Ca2+ release in permeabilized cells. On the contrary, dorsomorphin (EC50 = 0.4 μM) activated both histamine and IP3-induced Ca2+-release and reversed the effect of A769662. These results suggest a direct effect of AMPK regulation on IP3 receptor (IP3R) function. A phosphoproteomic study did not reveal changes in IP3R phosphorylation, but showed significant changes in phosphorylation of proteins placed upstream in the IP3R interactome and in several proteins related with Ca2+ metabolism, which could be candidates to mediate the effects observed. In conclusion, our data suggest that AMPK negatively regulates IP3R. This effect constitutes a novel and very important link between Ca2+ signaling and the AMPK pathway.
Publisher version (URL)https://doi.org/10.1016/j.ceca.2018.12.004
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