<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Tripathi R</submitter><pubmed_abstract>Glutamate acts as a critical regulator of neurotransmitter balance, recycling, synaptic function and homeostasis in the brain and glutamate transporters control glutamate levels in the brain. SLC38A10 is a member of the SLC38 family and regulates protein synthesis and cellular stress responses. Here, we uncover the role of SLC38A10 as a transceptor involved in glutamate-sensing signaling pathways that control both the glutamate homeostasis and mTOR-signaling. The culture of primary cortex cells from SLC38A10 knockout mice had increased intracellular glutamate. In addition, under nutrient starvation, KO cells had an impaired response in amino acid-dependent mTORC1 signaling. Combined studies from transcriptomics, protein arrays and metabolomics established that SLC38A10 is involved in mTOR </pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pagination>854397</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9017388</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SLC38A10 Regulate Glutamate Homeostasis and Modulate the AKT/TSC2/mTOR Pathway in Mouse Primary Cortex Cells.</pubmed_title><pmcid>PMC9017388</pmcid><pubmed_authors>Aggarwal T</pubmed_authors><pubmed_authors>Lindberg FA</pubmed_authors><pubmed_authors>Fredriksson R</pubmed_authors><pubmed_authors>Klemm AH</pubmed_authors><pubmed_authors>Tripathi R</pubmed_authors></additional><is_claimable>false</is_claimable><name>SLC38A10 Regulate Glutamate Homeostasis and Modulate the AKT/TSC2/mTOR Pathway in Mouse Primary Cortex Cells.</name><description>Glutamate acts as a critical regulator of neurotransmitter balance, recycling, synaptic function and homeostasis in the brain and glutamate transporters control glutamate levels in the brain. SLC38A10 is a member of the SLC38 family and regulates protein synthesis and cellular stress responses. Here, we uncover the role of SLC38A10 as a transceptor involved in glutamate-sensing signaling pathways that control both the glutamate homeostasis and mTOR-signaling. The culture of primary cortex cells from SLC38A10 knockout mice had increased intracellular glutamate. In addition, under nutrient starvation, KO cells had an impaired response in amino acid-dependent mTORC1 signaling. Combined studies from transcriptomics, protein arrays and metabolomics established that SLC38A10 is involved in mTOR </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-04-08T10:32:08.779Z</modification><creation>2024-11-09T18:54:38.056Z</creation></dates><accession>S-EPMC9017388</accession><cross_references><pubmed>35450293</pubmed><doi>10.3389/fcell.2022.854397</doi></cross_references></HashMap>