Structural determinants and regulation of spontaneous activity in GABAA receptors

Craig A. Sexton, Reka Penzinger, Martin Mortensen, Damian P. Bright and Trevor G. Smart ()
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Craig A. Sexton: Physiology & Pharmacology, UCL
Reka Penzinger: Physiology & Pharmacology, UCL
Martin Mortensen: Physiology & Pharmacology, UCL
Damian P. Bright: Physiology & Pharmacology, UCL
Trevor G. Smart: Physiology & Pharmacology, UCL

Nature Communications, 2021, vol. 12, issue 1, 1-18

Abstract: Abstract GABAA receptors are vital for controlling neuronal excitability and can display significant levels of constitutive activity that contributes to tonic inhibition. However, the mechanisms underlying spontaneity are poorly understood. Here we demonstrate a strict requirement for β3 subunit incorporation into receptors for spontaneous gating, facilitated by α4, α6 and δ subunits. The crucial molecular determinant involves four amino acids (GKER) in the β3 subunit’s extracellular domain, which interacts with adjacent receptor subunits to promote transition to activated, open channel conformations. Spontaneous activity is further regulated by β3 subunit phosphorylation and by allosteric modulators including neurosteroids and benzodiazepines. Promoting spontaneous activity reduced neuronal excitability, indicating that spontaneous currents will alter neural network activity. This study demonstrates how regional diversity in GABAA receptor isoform, protein kinase activity, and neurosteroid levels, can impact on tonic inhibition through the modulation of spontaneous GABAA receptor gating.

Date: 2021
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DOI: 10.1038/s41467-021-25633-0

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