Patterned expression of Purkinje cell glutamate transporters controls synaptic plasticity
Glutamate transporters are responsible for clearing synaptically released glutamate from the extracellular space. If expressed at high enough densities, transporters can prevent activation of extrasynaptic receptors by rapidly lowering glutamate concentrations to insignificant levels. We find that s...
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Veröffentlicht in: | Nature neuroscience 2005-10, Vol.8 (10), p.1329-1334 |
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description | Glutamate transporters are responsible for clearing synaptically released glutamate from the extracellular space. If expressed at high enough densities, transporters can prevent activation of extrasynaptic receptors by rapidly lowering glutamate concentrations to insignificant levels. We find that synaptic activation of metabotropic glutamate receptors expressed by Purkinje cells is prevented in regions of rat cerebellum where the density of the glutamate transporter EAAT4 is high. The consequences of metabotropic receptor stimulation, including activation of a depolarizing conductance, cannabinoid-mediated presynaptic inhibition and long-term depression, are also limited in Purkinje cells expressing high levels of EAAT4. We conclude that neuronal uptake sites must be overwhelmed by glutamate to activate perisynaptic metabotropic glutamate receptors. Regional differences in glutamate transporter expression affect the degree of metabotropic glutamate receptor activation and therefore regulate synaptic plasticity. |
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If expressed at high enough densities, transporters can prevent activation of extrasynaptic receptors by rapidly lowering glutamate concentrations to insignificant levels. We find that synaptic activation of metabotropic glutamate receptors expressed by Purkinje cells is prevented in regions of rat cerebellum where the density of the glutamate transporter EAAT4 is high. The consequences of metabotropic receptor stimulation, including activation of a depolarizing conductance, cannabinoid-mediated presynaptic inhibition and long-term depression, are also limited in Purkinje cells expressing high levels of EAAT4. We conclude that neuronal uptake sites must be overwhelmed by glutamate to activate perisynaptic metabotropic glutamate receptors. 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If expressed at high enough densities, transporters can prevent activation of extrasynaptic receptors by rapidly lowering glutamate concentrations to insignificant levels. We find that synaptic activation of metabotropic glutamate receptors expressed by Purkinje cells is prevented in regions of rat cerebellum where the density of the glutamate transporter EAAT4 is high. The consequences of metabotropic receptor stimulation, including activation of a depolarizing conductance, cannabinoid-mediated presynaptic inhibition and long-term depression, are also limited in Purkinje cells expressing high levels of EAAT4. We conclude that neuronal uptake sites must be overwhelmed by glutamate to activate perisynaptic metabotropic glutamate receptors. Regional differences in glutamate transporter expression affect the degree of metabotropic glutamate receptor activation and therefore regulate synaptic plasticity.</description><subject>alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology</subject><subject>Analysis of Variance</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Aspartic Acid - pharmacology</subject><subject>Behavioral Sciences</subject><subject>Biological Techniques</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Calcium - pharmacology</subject><subject>Cannabinoids - pharmacology</subject><subject>Carrier proteins</subject><subject>Cerebellum - cytology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Interactions</subject><subject>Excitatory Amino Acid Agonists - pharmacology</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Excitatory Amino Acid Transporter 4 - 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If expressed at high enough densities, transporters can prevent activation of extrasynaptic receptors by rapidly lowering glutamate concentrations to insignificant levels. We find that synaptic activation of metabotropic glutamate receptors expressed by Purkinje cells is prevented in regions of rat cerebellum where the density of the glutamate transporter EAAT4 is high. The consequences of metabotropic receptor stimulation, including activation of a depolarizing conductance, cannabinoid-mediated presynaptic inhibition and long-term depression, are also limited in Purkinje cells expressing high levels of EAAT4. We conclude that neuronal uptake sites must be overwhelmed by glutamate to activate perisynaptic metabotropic glutamate receptors. Regional differences in glutamate transporter expression affect the degree of metabotropic glutamate receptor activation and therefore regulate synaptic plasticity.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>16136036</pmid><doi>10.1038/nn1539</doi><tpages>6</tpages></addata></record> |
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subjects | alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology Analysis of Variance Animal Genetics and Genomics Animals Animals, Newborn Aspartic Acid - pharmacology Behavioral Sciences Biological Techniques Biomedical and Life Sciences Biomedicine Calcium - pharmacology Cannabinoids - pharmacology Carrier proteins Cerebellum - cytology Dose-Response Relationship, Drug Drug Interactions Excitatory Amino Acid Agonists - pharmacology Excitatory Amino Acid Antagonists - pharmacology Excitatory Amino Acid Transporter 4 - metabolism Excitatory Postsynaptic Potentials - physiology Excitatory Postsynaptic Potentials - radiation effects Gene Expression Regulation - drug effects Gene Expression Regulation - physiology Glutamic Acid - metabolism In Vitro Techniques Long-Term Synaptic Depression - drug effects Long-Term Synaptic Depression - physiology Membrane Potentials - drug effects Membrane Potentials - physiology Membrane Potentials - radiation effects Methoxyhydroxyphenylglycol - analogs & derivatives Methoxyhydroxyphenylglycol - pharmacology Neurobiology Neuronal Plasticity - physiology Neuroplasticity Neurosciences Patch-Clamp Techniques - methods Physiological aspects Purkinje cells Purkinje Cells - physiology Quinoxalines - pharmacology Rats Synapses - metabolism |
title | Patterned expression of Purkinje cell glutamate transporters controls synaptic plasticity |
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