Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.

GABA is the major inhibitory neurotransmitter in the adult brain and mechanisms of GABAergic inhibition have been intensely investigated in the past decades. Recent studies provided evidence for an important role of astrocytes in shaping GABAergic currents. One of the most obvious, but yet poorly un...

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Main Authors: Przemysław eKaczor, Dariusz eRakus, Jerzy Władysław Mozrzymas
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-04-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00120/full
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spelling doaj-86fd184b05f24be4b119f6c40d019af12020-11-24T22:27:31ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022015-04-01910.3389/fncel.2015.00120129427Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.Przemysław eKaczor0Dariusz eRakus1Jerzy Władysław Mozrzymas2Jerzy Władysław Mozrzymas3Uniwesytet WrocławskiUniwesytet WrocławskiUniwesytet WrocławskiWroclaw Medical UniversityGABA is the major inhibitory neurotransmitter in the adult brain and mechanisms of GABAergic inhibition have been intensely investigated in the past decades. Recent studies provided evidence for an important role of astrocytes in shaping GABAergic currents. One of the most obvious, but yet poorly understood, mechanisms of the cross-talk between GABAergic currents and astrocytes is metabolism including neurotransmitter homeostasis. In particular, how modulation of GABAergic currents by astrocytes depends on key enzymes involved in cellular metabolism remains largely unknown. To address this issue, we have considered two simple models of neuronal cultures: nominally astrocyte-free neuronal culture (NC) and neuronal-astrocytic co-cultures (ANCC) and miniature Inhibitory Postsynaptic Currents (mIPSCs) were recorded in control conditions and in the presence of respective enzyme blockers. We report that enrichment of neuronal culture with astrocytes results in a marked increase in mIPSC frequency. This enhancement of GABAergic activity was accompanied by increased number of GAD65 and vGAT puncta, indicating that at least a part of the frequency enhancement was due to increased number of synaptic contacts. Inhibition of glutamine synthetase (with MSO) strongly reduced mIPSC frequency in ANCC but had no effect in NC. Moreover, treatment of ANCC with inhibitor of glycogen phosphorylase (BAYU6751) or with selective inhibitor of astrocytic Krebs cycle,fluoroacetate, resulted in a marked reduction of mIPSC frequency in ANCC having no effect in NC. We conclude that GABAergic synaptic transmission strongly depends on neuron-astrocyte interaction in a manner dependent on key metabolic enzymes as well as on the Krebs cycle.http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00120/fullAstrocytesGlycogen PhosphorylaseMetabolismhippocampal neuronsGABAergic synapsesglutamine synthetase
collection DOAJ
language English
format Article
sources DOAJ
author Przemysław eKaczor
Dariusz eRakus
Jerzy Władysław Mozrzymas
Jerzy Władysław Mozrzymas
spellingShingle Przemysław eKaczor
Dariusz eRakus
Jerzy Władysław Mozrzymas
Jerzy Władysław Mozrzymas
Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
Frontiers in Cellular Neuroscience
Astrocytes
Glycogen Phosphorylase
Metabolism
hippocampal neurons
GABAergic synapses
glutamine synthetase
author_facet Przemysław eKaczor
Dariusz eRakus
Jerzy Władysław Mozrzymas
Jerzy Władysław Mozrzymas
author_sort Przemysław eKaczor
title Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
title_short Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
title_full Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
title_fullStr Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
title_full_unstemmed Neuron-astrocyte interaction enhance GABAergic synaptic transmission in a manner dependent on key metabolic enzymes.
title_sort neuron-astrocyte interaction enhance gabaergic synaptic transmission in a manner dependent on key metabolic enzymes.
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2015-04-01
description GABA is the major inhibitory neurotransmitter in the adult brain and mechanisms of GABAergic inhibition have been intensely investigated in the past decades. Recent studies provided evidence for an important role of astrocytes in shaping GABAergic currents. One of the most obvious, but yet poorly understood, mechanisms of the cross-talk between GABAergic currents and astrocytes is metabolism including neurotransmitter homeostasis. In particular, how modulation of GABAergic currents by astrocytes depends on key enzymes involved in cellular metabolism remains largely unknown. To address this issue, we have considered two simple models of neuronal cultures: nominally astrocyte-free neuronal culture (NC) and neuronal-astrocytic co-cultures (ANCC) and miniature Inhibitory Postsynaptic Currents (mIPSCs) were recorded in control conditions and in the presence of respective enzyme blockers. We report that enrichment of neuronal culture with astrocytes results in a marked increase in mIPSC frequency. This enhancement of GABAergic activity was accompanied by increased number of GAD65 and vGAT puncta, indicating that at least a part of the frequency enhancement was due to increased number of synaptic contacts. Inhibition of glutamine synthetase (with MSO) strongly reduced mIPSC frequency in ANCC but had no effect in NC. Moreover, treatment of ANCC with inhibitor of glycogen phosphorylase (BAYU6751) or with selective inhibitor of astrocytic Krebs cycle,fluoroacetate, resulted in a marked reduction of mIPSC frequency in ANCC having no effect in NC. We conclude that GABAergic synaptic transmission strongly depends on neuron-astrocyte interaction in a manner dependent on key metabolic enzymes as well as on the Krebs cycle.
topic Astrocytes
Glycogen Phosphorylase
Metabolism
hippocampal neurons
GABAergic synapses
glutamine synthetase
url http://journal.frontiersin.org/Journal/10.3389/fncel.2015.00120/full
work_keys_str_mv AT przemysławekaczor neuronastrocyteinteractionenhancegabaergicsynaptictransmissioninamannerdependentonkeymetabolicenzymes
AT dariuszerakus neuronastrocyteinteractionenhancegabaergicsynaptictransmissioninamannerdependentonkeymetabolicenzymes
AT jerzywładysławmozrzymas neuronastrocyteinteractionenhancegabaergicsynaptictransmissioninamannerdependentonkeymetabolicenzymes
AT jerzywładysławmozrzymas neuronastrocyteinteractionenhancegabaergicsynaptictransmissioninamannerdependentonkeymetabolicenzymes
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