Literature DB >> 15561425

Immunohistochemical localization of the amino acid transporter SNAT2 in the rat brain.

I M González-González1, B Cubelos, C Giménez, F Zafra.   

Abstract

SNAT2 is a neutral amino acid carrier that belongs to the system A family. Since its function in the nervous system remains unclear, we have analyzed its distribution in the rat CNS using specific antisera. Although SNAT2 is expressed widely in the CNS, it is enriched in the spinal cord and the brainstem nuclei, especially those of the auditory system. At the cellular level, SNAT2 was preferentially located in neuronal cell bodies and processes, although it was also strongly expressed in the meninges and ependyma. In astrocytes, the localization of SNAT2 was more restricted since it was intensely expressed in the perivascular end-feet, glia limitans, cerebellar astrocytes and Bergmann glia, but it was less intense in astrocytes of the cerebral parenchyma. Among neurons, the primary sensory neurons of the mesencephalic trigeminal nucleus appeared to be those that most strongly express SNAT2, but many other neurons, including cortical pyramidal cells and their dendrites were also intensely stained. In several regions the transporter was detected in axons, especially in the brainstem, and its presence in both dendrites and axons was confirmed by confocal microscopy and ultrastructural studies. However, while SNAT2 was observed in the large principal dendrites and the small distal dendrites, it was only found in axonal shafts and was excluded from terminals. Some glutamatergic neurons were among the more intensely labeled cells whereas SNAT2 was not detected on GABAergic neurons. The expression of SNAT2 partially coincides with that reported for SNAT1, especially in glutamatergic neurons. Hence, both proteins could fulfill complementary roles in replenishing glutamate pools and be differentially regulated under different physiological conditions. They also seem to co-localize in non-neuronal cells probably contributing to amino acid fluxes through the blood-brain barrier.

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Year:  2005        PMID: 15561425     DOI: 10.1016/j.neuroscience.2004.09.023

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  25 in total

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Review 3.  In vivo N-15 MRS study of glutamate metabolism in the rat brain.

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Journal:  Anal Biochem       Date:  2016-08-28       Impact factor: 3.365

4.  Electrographic seizures are significantly reduced by in vivo inhibition of neuronal uptake of extracellular glutamine in rat hippocampus.

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5.  Activity- and age-dependent modulation of GABAergic neurotransmission by system A-mediated glutamine uptake.

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6.  Modulation of epileptiform activity by glutamine and system A transport in a model of post-traumatic epilepsy.

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

Authors:  A Blot; D Billups; M Bjørkmo; A Z Quazi; N M Uwechue; F A Chaudhry; B Billups
Journal:  Neuroscience       Date:  2009-09-12       Impact factor: 3.590

8.  The evolutionary history and tissue mapping of amino acid transporters belonging to solute carrier families SLC32, SLC36, and SLC38.

Authors:  Björn E Sundberg; Elin Wååg; Josefin A Jacobsson; Olga Stephansson; Juris Rumaks; Simons Svirskis; Johan Alsiö; Erika Roman; Ted Ebendal; Vija Klusa; Robert Fredriksson
Journal:  J Mol Neurosci       Date:  2008-04-17       Impact factor: 3.444

9.  Brain interstitial fluid glutamine homeostasis is controlled by blood-brain barrier SLC7A5/LAT1 amino acid transporter.

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Journal:  J Cereb Blood Flow Metab       Date:  2015-10-19       Impact factor: 6.200

10.  Deletion of v7-3 (SLC6A15) transporter allows assessment of its roles in synaptosomal proline uptake, leucine uptake and behaviors.

Authors:  Jana Drgonova; Qing-Rong Liu; F Scott Hall; Rachael M Krieger; George R Uhl
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