Unravelling the Physiological Roles of GPCR Voltage Dependence

HORIZON.1.1HORIZON-ERCID: 101085605
EC Contribution
€19,925
Consortium Size
1 orgs
Summary

G protein coupled receptors (GPCRs) are broadly expressed in the brain, mediate responses to many molecules, and are crucial for normal brain function and therapeutic intervention.20 years ago, it was shown that the activity of many GPCRs is regulated by membrane potential. e.g. the activity of cholinergic M2R muscarinic and metabotropic glutamate mGluR3 receptors is reduced by depolarization, and that of M1R and mGluR1a is increased. However, due to high technical challenges, a crucial question remains unanswered: what are the physiological roles of this voltage dependency, its effect on neural activity, or its relevance to behaviour?Recently, we showed that M1R voltage dependence is crucial for its recruitment. Not only that under physiological conditions, in vivo, M1R could not be activated without depolarization, depolarization alone was sufficient to activate M1R. Furthermore, flies with a voltage independent M1R had increased odor habituation indicating a paramount effect on behavior. These findings are pivotal in our thinking on GPCR recruitment and activity. However, to create a real paradigm shift, we need to unravel whether GPCR voltage dependence has a role in other types of GPCRs and neuronal processes.The fly is an ideal model system to explore GPCR voltage dependence roles because it has a low variety of receptors with no functional overlap. In particular, the Drosophila dopaminergic and muscarinic receptors that are highly expressed in the olfactory system seem ideal. I will use a multidisciplinary approach of electrophysiology, two-photon imaging, genetics, and behaviour to examine GPCR voltage dependency and means to manipulate it, unravel these GPCR physiological roles, and examine whether abolishing GPCR voltage dependence affects neuronal activity and behavioural output. The understanding that there is a voltage rheostat that controls GPCR activity will open an entirely new field of research and can serve for new therapeutic intervention.

Consortium (1)

Project Results (5)

Source: CORDIS, the EU research results database.

Publications (5)
Current Biology
Current Biology· 2025DOI
Manoim-Wolkovitz, Julia E.; Camchy, Tal; Rozenfeld, Eyal; Chang, Hao-Hsin; Lerner, Hadas; Chou, Ya-Hui; Darshan, Ran; Parnas, Moshe
Ectopic sodium channel expression decreases excitability of <i>Drosophila</i> Kenyon cells
The Journal of Physiology· 2025DOI
Katie Greenin‐Whitehead, Eyal Rozenfeld, Anthony Moreno‐Sanchez, Melissa W. Tan, Kurtulus Kullu, Jessica Ausborn, Moshe Parnas, Andrew C. Lin
A highly conserved A-to-I RNA editing event within the glutamate-gated chloride channel GluClα is necessary for olfactory-based behaviors in <i>Drosophila</i>
Science Advances· 2024DOI
Hila Zak; Eyal Rozenfeld; Mali Levi; Patricia Deng; David Gorelick; Hadar Pozeilov; Shai Israel; Yoav Paas; Yoav Paas; Jin Billy Li; Moshe Parnas; Galit Shohat-Ophir
Learning and Memory
Learning & Memory· 2024DOI
Moshe Parnas; Julia E. Manoim; Andrew C. Lin
Neuronal circuit mechanisms of competitive interaction between action-based and coincidence learning
Science Advances· 2024DOI
Eyal Rozenfeld; Moshe Parnas