bioRxiv Science⌕ Search

Biology subjects

Bui, D. L. H.

Publications and source records attributed to Bui, D. L. H..

2 recordsLinked to original sources

The atypical adhesion GPCR ADGRA1 controls hippocampal inhibitory circuit function

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 synaptic function are unclear. Here, we identify the atypical adhesion GPCR ADGRA1 as essential for hippocampal PV and SST inhibitory synaptic function. ADGRA1 is selectively enriched in hippocampal PV and SST interneurons and localizes to a subset of synapses. ADGRA1 deletion in PV and SST interneurons impairs inhibitory synaptic inputs onto Dentate Gyrus granule cells and generates deficits in learning and memory. ADGRA1 engages several downstream G proteins, notably G13, a pathway important for the establishment of hippocampal PV interneuron synaptic networks. These results identify an orphan receptor pathway selective for specific inhibitory synapse subtypes and expand our understanding of the signaling mechanisms that establish hippocampal inhibitory circuits.

neuroscience↗

The adhesion GPCRs CELSR1-3 and LPHN3 engage G proteins via distinct activation mechanisms

Adhesion GPCRs (aGPCRs) are a large GPCR class that direct diverse fundamental biological processes. One prominent mechanism for aGPCR agonism involves autoproteolytic cleavage, which generates an activating, membrane-proximal tethered agonist (TA). How universal this mechanism is for all aGPCRs is unclear. Here, we investigate G protein induction principles of aGPCRs using mammalian LPHN3 and CELSR1-3, members of two aGPCR families conserved from invertebrates to vertebrates. LPHNs and CELSRs mediate fundamental aspects of brain development, yet CELSR signaling mechanisms are unknown. We found that CELSR1 and CELSR3 are cleavage-deficient, while CELSR2 is efficiently cleaved. Despite differential autoproteolysis, CELSR1-3 all engage GS, and CELSR1 or CELSR3 TA point mutants retain GS coupling activity. CELSR2 autoproteolysis enhances GS coupling, yet acute TA exposure alone is insufficient. These studies support that aGPCRs signal via multiple paradigms and provide insights into CELSR biological function.

cell biology↗