Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 114, Issue 44, Pages 11763-11768Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.1705075114
Keywords
estrogen; inhibition; synapse
Categories
Funding
- AstraZeneca
- program Investissements d'Avenir [ANR-10-LABX-54 MEMO LIFE, ANR-11-IDEX-0001-02]
- European Research Council advanced research grant Plasltlnhib
- Agence Nationale de la Recherche Synaptune (Programme blanc) [ANR-12-BSV4-0019-01]
- Tufts Center for Neuroscience Research [P30 NS047243]
- NIH, National Institute of Neurological Disorders and Stroke [R01 NS073574]
- Department of Defense Grant [AR140209]
- NIH [NS051195, NS081986, MH097446, DA037170-01, 1R01NS087662, MH106954]
- Medical Research Council [MR/L021064/1]
- Institut National de la Sante et de la Recherche Medicale
- Alzheimers Research UK [ARUK-PhD2016-4] Funding Source: researchfish
- Medical Research Council [MR/N026063/1, MR/L021064/1] Funding Source: researchfish
- Agence Nationale de la Recherche (ANR) [ANR-12-BSV4-0019] Funding Source: Agence Nationale de la Recherche (ANR)
- MRC [MR/L021064/1, MR/N026063/1] Funding Source: UKRI
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Estrogen plays a critical role in many physiological processes and exerts profound effects on behavior by regulating neuronal excitability. While estrogen has been established to exert effects on dendritic morphology and excitatory neurotransmission its role in regulating neuronal inhibition is poorly understood. Fast synaptic inhibition in the adult brain is mediated by specialized populations of gamma-c a(A) receptors (GABA(A) Rs) that are selectively enriched at syn-apses, a process dependent upon their interaction with the inhibitory scaffold protein gephyrin. Here we have assessed the role that estradiol (E2) plays in regulating the dynamics of GABA a Rs and stability of inhibitory synapses. Treatment of cultured cortical neurons with E2 reduced the accumulation of GABA a Rs and gephyrin at inhibitory synapses. However, E2 exposure did not modify the ex pression of either the total or the plasma membrane GABA a Rs or gephyrin. Mechanistically, single-particle tracking revealed that E2 treatment selectively reduced the dwell time and thereby decreased the confinement of GABA a Rs at inhibitory synapses. Consistent with our cell biology measurements, we observed a significant reduction in amplitude of inhibitory synaptic currents in both cultured neurons and hippocampal slices exposed to E2, while their frequency was unaffected. Collectively, our results suggest that acute exposure of neurons to E2 leads to destabilization of GABA a Rs and gephyrin at inhibitory synapses, leading to reductions in the efficacy of GABAergic inhibition via a postsynaptic mechanism.
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