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Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons

Glutamine plays multiple roles in the CNS, including metabolic functions and production of the neurotransmitters glutamate and GABA. It has been proposed to be taken up into neurons via a variety of membrane transport systems, including system A, which is a sodium-dependent electrogenic amino acid t...

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Detalles Bibliográficos
Autores principales: Blot, A., Billups, D., Bjørkmo, M., Quazi, A.Z., Uwechue, N.M., Chaudhry, F.A., Billups, B.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789247/
https://www.ncbi.nlm.nih.gov/pubmed/19751803
http://dx.doi.org/10.1016/j.neuroscience.2009.09.015
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author Blot, A.
Billups, D.
Bjørkmo, M.
Quazi, A.Z.
Uwechue, N.M.
Chaudhry, F.A.
Billups, B.
author_facet Blot, A.
Billups, D.
Bjørkmo, M.
Quazi, A.Z.
Uwechue, N.M.
Chaudhry, F.A.
Billups, B.
author_sort Blot, A.
collection PubMed
description Glutamine plays multiple roles in the CNS, including metabolic functions and production of the neurotransmitters glutamate and GABA. It has been proposed to be taken up into neurons via a variety of membrane transport systems, including system A, which is a sodium-dependent electrogenic amino acid transporter system. In this study, we investigate glutamine transport by application of amino acids to individual principal neurons of the medial nucleus of the trapezoid body (MNTB) in acutely isolated rat brain slices. A glutamine transport current was studied in patch-clamped neurons, which had the electrical and pharmacological properties of system A: it was sodium-dependent, had a non-reversing current-voltage relationship, was activated by proline, occluded by N-(methylamino)isobutyric acid (MeAIB), and was unaffected by 2-aminobicyclo-[2.2.1]-heptane-2-carboxylic acid (BCH). Additionally, we examined the expression of different system A transporter isoforms using immunocytochemical staining with antibodies raised against system A transporter 1 and 2 (SAT1 and SAT2). Our results indicate that both isoforms are expressed in MNTB principal neurons, and demonstrate that functional system A transporters are present in the plasma membrane of neurons. Since system A transport is highly regulated by a number of cellular signaling mechanisms and glutamine then goes on to activate other pathways, the study of these transporters in situ gives an indication of the mechanisms of neuronal glutamine supply as well as points of regulation of neurotransmitter production, cellular signaling and metabolism in the native neuronal environment.
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spelling pubmed-27892472009-12-22 Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons Blot, A. Billups, D. Bjørkmo, M. Quazi, A.Z. Uwechue, N.M. Chaudhry, F.A. Billups, B. Neuroscience Cellular Neuroscience Glutamine plays multiple roles in the CNS, including metabolic functions and production of the neurotransmitters glutamate and GABA. It has been proposed to be taken up into neurons via a variety of membrane transport systems, including system A, which is a sodium-dependent electrogenic amino acid transporter system. In this study, we investigate glutamine transport by application of amino acids to individual principal neurons of the medial nucleus of the trapezoid body (MNTB) in acutely isolated rat brain slices. A glutamine transport current was studied in patch-clamped neurons, which had the electrical and pharmacological properties of system A: it was sodium-dependent, had a non-reversing current-voltage relationship, was activated by proline, occluded by N-(methylamino)isobutyric acid (MeAIB), and was unaffected by 2-aminobicyclo-[2.2.1]-heptane-2-carboxylic acid (BCH). Additionally, we examined the expression of different system A transporter isoforms using immunocytochemical staining with antibodies raised against system A transporter 1 and 2 (SAT1 and SAT2). Our results indicate that both isoforms are expressed in MNTB principal neurons, and demonstrate that functional system A transporters are present in the plasma membrane of neurons. Since system A transport is highly regulated by a number of cellular signaling mechanisms and glutamine then goes on to activate other pathways, the study of these transporters in situ gives an indication of the mechanisms of neuronal glutamine supply as well as points of regulation of neurotransmitter production, cellular signaling and metabolism in the native neuronal environment. Elsevier Science 2009-12-15 /pmc/articles/PMC2789247/ /pubmed/19751803 http://dx.doi.org/10.1016/j.neuroscience.2009.09.015 Text en © 2009 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Cellular Neuroscience
Blot, A.
Billups, D.
Bjørkmo, M.
Quazi, A.Z.
Uwechue, N.M.
Chaudhry, F.A.
Billups, B.
Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title_full Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title_fullStr Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title_full_unstemmed Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title_short Functional expression of two system A glutamine transporter isoforms in rat auditory brainstem neurons
title_sort functional expression of two system a glutamine transporter isoforms in rat auditory brainstem neurons
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789247/
https://www.ncbi.nlm.nih.gov/pubmed/19751803
http://dx.doi.org/10.1016/j.neuroscience.2009.09.015
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