Gα q -coupled receptors activate cAMP signaling through Ca 2+ /calmodulin-stimulated adenylyl cyclases
Among the various G protein–mediated intracellular signaling pathways activated by G protein–coupled receptors (GPCRs), Gα s and Gα i stimulate and inhibit adenylyl cyclases (ADCYs), leading to increases and decreases in cAMP abundance, respectively. Here, we investigated the contribution of Gα q -coupled receptors (Gα q -GPCRs), which typically activate phospholipase C (PLC) and stimulate intracellular Ca 2+ generation, to the regulation of cAMP signaling. We activated the endogenous Gα q -coupled muscarinic acetylcholine receptors (Gα q -mAChRs) and the group 1 metabotropic glutamate receptors (mGluR1/5) in ex vivo hippocampal slices from mice. We also used a chemogenetics approach to activate Gα q -DREADDs (designer receptors exclusively activated by designer drugs) through hM3Dq. We found that stimulation of these Gα q -GPCRs not only increased the abundance of cAMP but also activated downstream, cAMP-mediated intracellular signaling pathways. This GPCR-dependent cAMP signaling required both Gα q activity and intracellular Ca 2+ . Additionally, hippocampal slices from mice lacking the Ca 2+ /calmodulin-stimulated ADCYs, ADCY1 and ADCY8, did not exhibit Gα q -GPCR–mediated cAMP signaling and showed impaired synaptic long-term depression (LTD) mediated by Gα q -mAChRs. Together, our findings highlight a nonconventional function of Gα q -GPCRs in regulating cAMP signaling through distinct ADCYs.
Authors
- Qi Ding (ORCID: https://orcid.org/0000-0003-0216-5856)
- N. Williams (ORCID: https://orcid.org/0009-0007-1186-8744)
- Lulu An (ORCID: https://orcid.org/0000-0002-3036-1689)
- Hongbing Wang (ORCID: https://orcid.org/0000-0002-7362-7854)
- Jianhua Ren
Institutions
- Michigan State University (US)
Publication Details
- Journal
- Science Signaling
- Published
- 2026-11-03
- DOI
- https://doi.org/10.1126/scisignal.adv3154
- Primary Topic
- Receptor Mechanisms and Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.00