The atypical adhesion GPCR ADGRA1 controls hippocampal inhibitory circuit function
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Updated: Apr 12, 2026

Combined In Vivo Anatomical and Functional Tracing of Ventral Tegmental Area Glutamate Terminals in the Hippocampus
Published on: September 9, 2020
Baris Tosun1, Kelly Honkanen1, Elizabeth Orput1
1Department of Pharmacology, Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN 37240, USA.
Abstract:
Neural circuits contain a diverse array of inhibitory interneurons that control information processing. The cell surface receptors and signaling pathways that modulate cell-type-specific inhibitory function are unclear. Here, we identify the orphan G protein-coupled receptor (GPCR) ADGRA1 as essential for hippocampal PV inhibitory synaptic function. ADGRA1 is selectively enriched in hippocampal PV interneurons and localizes to a subset of synapses. ADGRA1 deletion in PV interneurons impairs intrinsic excitability and reduces inhibitory synaptic strength onto dentate gyrus granule cells. ADGRA1 engages several downstream G proteins, notably Gα13, a pathway important for the establishment of hippocampal PV interneuron synaptic networks. These results identify an orphan receptor pathway selective for fast-spiking PV neuron function and expand our understanding of the signaling mechanisms that establish hippocampal inhibitory circuits.

