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SLC38A9 is expressed in inhibitory and excitatory neurons and the gene expression changes in mouse brain after starvation and high-fat diet
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Functional Pharmacology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences.ORCID iD: 0000-0002-9681-5129
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Functional Pharmacology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Functional Pharmacology.
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(English)Manuscript (preprint) (Other academic)
National Category
Medical and Health Sciences Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:uu:diva-275722OAI: oai:DiVA.org:uu-275722DiVA: diva2:903041
Available from: 2016-02-12 Created: 2016-02-05 Last updated: 2017-10-12Bibliographically approved
In thesis
1. Characterization of Amino Acid Transporters: Transporters expressed in the central nervous system belonging to the Solute Carrier family SLC38
Open this publication in new window or tab >>Characterization of Amino Acid Transporters: Transporters expressed in the central nervous system belonging to the Solute Carrier family SLC38
2016 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

In cells and organelles transporters are responsible for translocation of amino acids, sugars and nucleotides among others. In the central nervous system (CNS), amino acid transporters can function as neurotransmitter transporters and nutrient sensors. The Solute carrier (SLC) superfamily is the largest family of transporters with 395 members divided in 52 families. The system A and system N amino acid transporter family, SLC38, consists of 11 members, SNAT1-11 (SLC38A1-11). The members are expressed in the brain, exclusively in neurons or astrocytes and some in both. Amino acid signaling is mainly regulated via two pathways, the amino acid responsive (AAR) pathway and the mechanistic/mammalian target of rapamycin complex 1 (mTORC1) pathway. These pathways regulate the protein synthesis in opposite directions depending on the amino acid availability. SLC38 members along with other SLCs have been identified to participate in these pathways.

In paper I, the regulation of SLC genes after complete amino acid starvation in mouse hypothalamic cells have been studied with microarray and we found that 47 SLC genes were significantly altered at five hours of starvation. Interestingly, we found that Slc38a1 and Slc38a7 were upregulated along with the known starvation responding gene, Slc38a2. A complementary starvation study for the SLC38 genes was performed using primary mouse embryonic cortex cells. We found that Slc38a1, Slc38a2, Slc38a5, Slc38a6 and Slc38a8 were upregulated while Slc38a3, Slc38a7 and Slc38a11 were downregulated.

Three members from the SLC38 family, SNAT8 (paper IV), SNAT9 (paper III) and SNAT10 (paper II) have been histologically characterized in mouse brain and all these transporters are exclusively neuronal. SNAT8 and SNAT10 were also functionally characterized and shown to be transporters for alanine and glutamine among others. SNAT8 was shown to mediate sodium dependent transport and was classified to system A. SNAT10 was shown to be a sodium independent bidirectional transporter and displayed characteristics for system A and N. SNAT9 is a lysosomal component of the Ragulator-Rag complex which senses amino acid availability and activates mTORC1. In paper III we also found that Slc38a9 gene expression was upregulated following starvation and downregulated following high-fat diet in mouse brain.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2016. 43 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1180
Keyword
Solute carriers, amino acid transporter, SLC38 family, SLC38A8, SNAT8, SLC38A10, SNAT10, SLC38A9, SNAT9, amino acid starvation, AAR, mTORC1
National Category
Medical and Health Sciences
Research subject
Neuroscience
Identifiers
urn:nbn:se:uu:diva-275723 (URN)978-91-554-9477-3 (ISBN)
Public defence
2016-04-01, B/A1:107a BMC, Biomedicinskt centrum Husargatan 3, Uppsala, 10:15 (English)
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Available from: 2016-03-11 Created: 2016-02-05 Last updated: 2016-03-17

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Hellsten, Sofie VictoraEriksson, MikaelaLekholm, EmiliaPerland, EmelieFredriksson, Robert

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