Skip to content
naulon
Not checkedNot checked for notices yet.

GABA A receptor dynamics and constructing GABAergic synapses

Verena Tretter, Stephen J Moss, Stephen J Moss

Frontiers in Molecular Neuroscience · 2008

doi:10.3389/neuro.02.007.2008 (opens in a new tab)

We email you when a new notice or a question about this paper appears.

Abstract

GABA <sub>A</sub> receptors are located on the majority of neurons in the central and peripheral nervous system, where they mediate important actions of the neurotransmitter gamma-aminobutyric acid. Early in development the trophic properties of GABA allow a healthy development of the nervous system. Most neurons have a high intracellular Cl- concentration early in live due to the late functional expression of the Cl-pump KCC2, therefore GABA has excitatory effects at this stage. Upon higher expression and activation of KCC2 GABA takes on its inhibitory effects while glutamate functions as the major excitatory neurotransmitter. Like all multisubunit membrane proteins the GABA<sub>A</sub> receptor is assembled in the ER and travels through the Golgi and remaining secretory pathway to the cell surface, where it mediates GABA actions either directly at the synapses or at extrasynaptic sites responding to ambient GABA to provide a basal tonic inhibitory state. In order to adapt to changing needs and information states, the GABAergic system is highly dynamic. That includes subtype specific trafficking to different locations in the cell, regulation of mobility by interaction with scaffold molecules, posttranslational modifications, that either directly affect channel function or the interaction with other proteins and finally the dynamic exchange between surface and intracellular receptor pools, that either prepare receptors for recycling to the surface or degradation. Here we give an overview of the current understanding of GABA<sub>A</sub>receptor functional and molecular dynamics that play a major part in major part in maintaining the balance between excitation and inhibition and in changes in network activity.

Abstract licence: CC BY

References173

    40 more references, whose wording the paper’s licence keeps private.

    All 173 references

    Reads

    Read by people on this page

    None yet.

    Checked or read by AI through naulon

    None yet.

    A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

    Are you an author?

    Is this your paper?

    Claim it to add your note and be paid when agents cite it. Free.