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                <identifier>oai:data.mendeley.com/n8d2ymd85h.1</identifier>
                <datestamp>2023-04-11T08:20:15Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator id="https://orcid.org/0000-0002-7535-5450">Krishnan, Karthik Subramanian</dc:creator>
    <dc:title>ASC transporters mediate D-serine transport into astrocytes adjacent to synapses in mouse brain</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Background: D-serine is an important signaling molecule, which activates N-methyl D-aspartate receptors (NMDARs) in conjunction with its fellow co-agonist, the neurotransmitter glutamate. 
Question: Despite its involvement in plasticity and memory related to excitatory synapses, its cellular source and sink remain a question. 
Importance: This removal of synaptic D-serine and its subsequent metabolic degradation is expected to reduce its extracellular availability, influencing NMDAR activation and NMDAR-dependent synaptic plasticity.
Hypothesis: We hypothesise that astrocytes, a type of glial cell that surround synapses are likely candidates to control the extracellular concentration of D-Serine by removing it from the synaptic space.
Notable finding:  We observed D-serine induced transport-associated currents upon puff-application of 10 mM D-serine on astrocytes. Further, O-benzyl-L-serine and trans-4-hydroxy-proline, known substrate inhibitors of the alanine serine cysteine transporters (ASCT) reduced D-serine uptake. These results indicate that ASCT is a central mediator of astrocytic D-serine transport and plays a role in regulating its synaptic concentration by sequestration into astrocytes. Similar results were observed in astrocytes of the somatosensory cortex and Bergmann glia in the cerebellum, indicative of a general mechanism expressed across a range of brain areas.
How was it gathered: We used patch clamping technique, to study the transmembrane electrical signals from individual identified astrocytes in the CA1 region of hippocampus, primary somatosensory cortex and Bergmann glia. It involved placing a tiny glass patch pipette, onto the surface of the astrocytic membrane, to record D-serine transporter currents. 
Methods: Using in situ patch clamp recordings and pharmacological manipulation of astrocytes in CA1 region of the mouse hippocampal brain slices, we investigated transport of D-serine across the plasma membrane. 
How to interpret data: The spread sheet contains all the mean astrocytic D-serine currents that were recorded from individual cells. 
How to use it: The raw data traces are most compatible with Clampfit 10.7.0.3 (P Clamp - Molecular devices 2016). </dc:description>
    <dc:subject>Neurotransmitter Transporter</dc:subject>
    <dc:subject>Membrane Electrophysiology</dc:subject>
    <dc:subject>Excitatory Amino Acids</dc:subject>
    <dc:subject>Amino Acid Metabolism</dc:subject>
    <dc:subject>Astrocyte</dc:subject>
    <dc:subject>Amino Acid Degradation</dc:subject>
    <dc:subject>Cellular Neuroscience</dc:subject>
    <dc:subject>Membrane Transport Proteins</dc:subject>
    <dc:subject>Patch Clamp Technique</dc:subject>
    <dc:subject>Voltage Clamp</dc:subject>
    <dc:subject>Serine</dc:subject>
    <dc:contributor id="https://orcid.org/0000-0001-5378-2809">Billups, Brian</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/n8d2ymd85h.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/n8d2ymd85h.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/n8d2ymd85h</dc:relation>
    <dc:date>2023-04-11T08:20:15Z</dc:date>
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