The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle

Research output: Book/ReportAnthologyResearchpeer-review

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The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle. / Leke, Renata; Schousboe, Arne.

2016. 35 p. (Advances in Neurobiology).

Research output: Book/ReportAnthologyResearchpeer-review

Harvard

Leke, R & Schousboe, A 2016, The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle. Advances in Neurobiology, vol. 13. https://doi.org/10.1007/978-3-319-45096-4_8

APA

Leke, R., & Schousboe, A. (2016). The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle. Advances in Neurobiology https://doi.org/10.1007/978-3-319-45096-4_8

Vancouver

Leke R, Schousboe A. The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle. 2016. 35 p. (Advances in Neurobiology). https://doi.org/10.1007/978-3-319-45096-4_8

Author

Leke, Renata ; Schousboe, Arne. / The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle. 2016. 35 p. (Advances in Neurobiology).

Bibtex

@book{d10ff1bf48684bfb94383c419f087b75,
title = "The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle",
abstract = "Glutamine is a key amino acid in the CNS, playing an important role in the glutamate/GABA-glutamine cycle (GGC). In the GGC, glutamine is transferred from astrocytes to neurons, where it will replenish the inhibitory and excitatory neurotransmitter pools. Different transporters participate in this neural communication, i.e., the transporters responsible for glutamine efflux from astrocytes and influx into the neurons, such as the members of the SNAT, LAT, y(+)LAT, and ASC families of transporters. The SNAT family consists of the transporter isoforms SNAT3 and SNAT5 that are related to efflux from the astrocytic compartment, and SNAT1 and SNAT2 that are associated with glutamine uptake into the neuronal compartment. The isoforms SNAT7 and SNAT8 do not have their role completely understood, but they likely also participate in the GGC. The isoforms LAT2 and y(+)LAT2 facilitate the exchange of neutral amino acids and cationic amino acids (y(+)LAT2 isoform) and have been associated with glutamine efflux from astrocytes. ASCT2 is a Na(+)-dependent antiporter, the participation of which in the GGC also remains to be better characterized. All these isoforms are tightly regulated by transcriptional and translational mechanisms, which are induced by several determinants such as amino acid deprivation, hormones, pH, and the activity of different signaling pathways. Dysfunctional glutamine transporter activity has been associated with the pathophysiological mechanisms of certain neurologic diseases, such as Hepatic Encephalopathy and Manganism. However, there might also be other neuropathological conditions associated with an altered GGC, in which glutamine transporters are dysfunctional. Hence, it appears to be of critical importance that the physiological and pathological aspects of glutamine transporters are thoroughly investigated.",
author = "Renata Leke and Arne Schousboe",
year = "2016",
doi = "10.1007/978-3-319-45096-4_8",
language = "English",
volume = "13",
series = "Advances in Neurobiology",
publisher = "Springer",

}

RIS

TY - BOOK

T1 - The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle

AU - Leke, Renata

AU - Schousboe, Arne

PY - 2016

Y1 - 2016

N2 - Glutamine is a key amino acid in the CNS, playing an important role in the glutamate/GABA-glutamine cycle (GGC). In the GGC, glutamine is transferred from astrocytes to neurons, where it will replenish the inhibitory and excitatory neurotransmitter pools. Different transporters participate in this neural communication, i.e., the transporters responsible for glutamine efflux from astrocytes and influx into the neurons, such as the members of the SNAT, LAT, y(+)LAT, and ASC families of transporters. The SNAT family consists of the transporter isoforms SNAT3 and SNAT5 that are related to efflux from the astrocytic compartment, and SNAT1 and SNAT2 that are associated with glutamine uptake into the neuronal compartment. The isoforms SNAT7 and SNAT8 do not have their role completely understood, but they likely also participate in the GGC. The isoforms LAT2 and y(+)LAT2 facilitate the exchange of neutral amino acids and cationic amino acids (y(+)LAT2 isoform) and have been associated with glutamine efflux from astrocytes. ASCT2 is a Na(+)-dependent antiporter, the participation of which in the GGC also remains to be better characterized. All these isoforms are tightly regulated by transcriptional and translational mechanisms, which are induced by several determinants such as amino acid deprivation, hormones, pH, and the activity of different signaling pathways. Dysfunctional glutamine transporter activity has been associated with the pathophysiological mechanisms of certain neurologic diseases, such as Hepatic Encephalopathy and Manganism. However, there might also be other neuropathological conditions associated with an altered GGC, in which glutamine transporters are dysfunctional. Hence, it appears to be of critical importance that the physiological and pathological aspects of glutamine transporters are thoroughly investigated.

AB - Glutamine is a key amino acid in the CNS, playing an important role in the glutamate/GABA-glutamine cycle (GGC). In the GGC, glutamine is transferred from astrocytes to neurons, where it will replenish the inhibitory and excitatory neurotransmitter pools. Different transporters participate in this neural communication, i.e., the transporters responsible for glutamine efflux from astrocytes and influx into the neurons, such as the members of the SNAT, LAT, y(+)LAT, and ASC families of transporters. The SNAT family consists of the transporter isoforms SNAT3 and SNAT5 that are related to efflux from the astrocytic compartment, and SNAT1 and SNAT2 that are associated with glutamine uptake into the neuronal compartment. The isoforms SNAT7 and SNAT8 do not have their role completely understood, but they likely also participate in the GGC. The isoforms LAT2 and y(+)LAT2 facilitate the exchange of neutral amino acids and cationic amino acids (y(+)LAT2 isoform) and have been associated with glutamine efflux from astrocytes. ASCT2 is a Na(+)-dependent antiporter, the participation of which in the GGC also remains to be better characterized. All these isoforms are tightly regulated by transcriptional and translational mechanisms, which are induced by several determinants such as amino acid deprivation, hormones, pH, and the activity of different signaling pathways. Dysfunctional glutamine transporter activity has been associated with the pathophysiological mechanisms of certain neurologic diseases, such as Hepatic Encephalopathy and Manganism. However, there might also be other neuropathological conditions associated with an altered GGC, in which glutamine transporters are dysfunctional. Hence, it appears to be of critical importance that the physiological and pathological aspects of glutamine transporters are thoroughly investigated.

UR - http://link.springer.com/chapter/10.1007%2F978-3-319-45096-4_8

U2 - 10.1007/978-3-319-45096-4_8

DO - 10.1007/978-3-319-45096-4_8

M3 - Anthology

C2 - 27885631

VL - 13

T3 - Advances in Neurobiology

BT - The Glutamine Transporters and Their Role in the Glutamate/GABA-Glutamine Cycle

ER -

ID: 169562397