A Reappraisal of GAT-1 Localization in Neocortex

γ-Aminobutyric acid (GABA) transporter (GAT)-1, the major GABA transporter in the brain, plays a key role in modulating GABA signaling and is involved in the pathophysiology of several neuropsychiatric diseases, including epilepsy. The original description of GAT-1 as a neuronal transporter has guid...

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Main Authors: Giorgia Fattorini, Marcello Melone, Fiorenzo Conti
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fncel.2020.00009/full
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spelling doaj-c8aa862e4e3f4995919d8c0c46a7e74f2020-11-25T00:34:37ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022020-02-011410.3389/fncel.2020.00009516017A Reappraisal of GAT-1 Localization in NeocortexGiorgia Fattorini0Giorgia Fattorini1Marcello Melone2Marcello Melone3Fiorenzo Conti4Fiorenzo Conti5Fiorenzo Conti6Department of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, Università Politecnica delle Marche, Ancona, ItalyCenter for Neurobiology of Aging, IRCCS INRCA, Ancona, ItalyDepartment of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, Università Politecnica delle Marche, Ancona, ItalyCenter for Neurobiology of Aging, IRCCS INRCA, Ancona, ItalyDepartment of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, Università Politecnica delle Marche, Ancona, ItalyCenter for Neurobiology of Aging, IRCCS INRCA, Ancona, ItalyFondazione di Medicina Molecolare, Università Politecnica delle Marche, Ancona, Italyγ-Aminobutyric acid (GABA) transporter (GAT)-1, the major GABA transporter in the brain, plays a key role in modulating GABA signaling and is involved in the pathophysiology of several neuropsychiatric diseases, including epilepsy. The original description of GAT-1 as a neuronal transporter has guided the interpretation of the findings of all physiological, pharmacological, genetic, or clinical studies. However, evidence published in the past few years, some of which is briefly reviewed herein, does not seem to be consistent with a neurocentric view of GAT-1 function and calls for more detailed analysis of its localization. We therefore performed a thorough systematic assessment of GAT-1 localization in neocortex and subcortical white matter. In line with earlier work, we found that GAT-1 was robustly expressed in axon terminals forming symmetric synapses and in astrocytic processes, whereas its astrocytic expression was more diffuse than expected and, even more surprisingly, immature and mature oligodendrocytes and microglial cells also expressed the transporter. These data indicate that the era of “neuronal” and “glial” GABA transporters has finally come to a close and provide a wider perspective from which to view GABA-mediated physiological phenomena. In addition, given the well-known involvement of astrocytes, oligodendrocytes, and microglial cells in physiological as well as pathological conditions, the demonstration of functional GAT-1 in these cells is expected to provide greater insight into the phenomena occurring in the diseased brain as well as to prompt a reassessment of earlier findings.https://www.frontiersin.org/article/10.3389/fncel.2020.00009/fullGAT-1GABA transportersastrocytesoligodendrocytesmicroglia
collection DOAJ
language English
format Article
sources DOAJ
author Giorgia Fattorini
Giorgia Fattorini
Marcello Melone
Marcello Melone
Fiorenzo Conti
Fiorenzo Conti
Fiorenzo Conti
spellingShingle Giorgia Fattorini
Giorgia Fattorini
Marcello Melone
Marcello Melone
Fiorenzo Conti
Fiorenzo Conti
Fiorenzo Conti
A Reappraisal of GAT-1 Localization in Neocortex
Frontiers in Cellular Neuroscience
GAT-1
GABA transporters
astrocytes
oligodendrocytes
microglia
author_facet Giorgia Fattorini
Giorgia Fattorini
Marcello Melone
Marcello Melone
Fiorenzo Conti
Fiorenzo Conti
Fiorenzo Conti
author_sort Giorgia Fattorini
title A Reappraisal of GAT-1 Localization in Neocortex
title_short A Reappraisal of GAT-1 Localization in Neocortex
title_full A Reappraisal of GAT-1 Localization in Neocortex
title_fullStr A Reappraisal of GAT-1 Localization in Neocortex
title_full_unstemmed A Reappraisal of GAT-1 Localization in Neocortex
title_sort reappraisal of gat-1 localization in neocortex
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2020-02-01
description γ-Aminobutyric acid (GABA) transporter (GAT)-1, the major GABA transporter in the brain, plays a key role in modulating GABA signaling and is involved in the pathophysiology of several neuropsychiatric diseases, including epilepsy. The original description of GAT-1 as a neuronal transporter has guided the interpretation of the findings of all physiological, pharmacological, genetic, or clinical studies. However, evidence published in the past few years, some of which is briefly reviewed herein, does not seem to be consistent with a neurocentric view of GAT-1 function and calls for more detailed analysis of its localization. We therefore performed a thorough systematic assessment of GAT-1 localization in neocortex and subcortical white matter. In line with earlier work, we found that GAT-1 was robustly expressed in axon terminals forming symmetric synapses and in astrocytic processes, whereas its astrocytic expression was more diffuse than expected and, even more surprisingly, immature and mature oligodendrocytes and microglial cells also expressed the transporter. These data indicate that the era of “neuronal” and “glial” GABA transporters has finally come to a close and provide a wider perspective from which to view GABA-mediated physiological phenomena. In addition, given the well-known involvement of astrocytes, oligodendrocytes, and microglial cells in physiological as well as pathological conditions, the demonstration of functional GAT-1 in these cells is expected to provide greater insight into the phenomena occurring in the diseased brain as well as to prompt a reassessment of earlier findings.
topic GAT-1
GABA transporters
astrocytes
oligodendrocytes
microglia
url https://www.frontiersin.org/article/10.3389/fncel.2020.00009/full
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