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      Vesicle Pool Heterogeneity at Hippocampal Glutamate and GABA Synapses

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          Abstract

          Glutamate and GABA are the major fast excitatory and inhibitory neurotransmitters, respectively, in the CNS. Although glutamate and GABA have clearly distinct postsynaptic actions, we are just beginning to appreciate that presynaptic differences between glutamatergic and GABAergic neurons may contribute to distinct functions of these transmitter systems. We therefore probed possible differences between the functional synaptic vesicle populations of glutamatergic and GABAergic neurons. We examined superecliptic synaptopHluorin (SpH) fluorescence during 20 Hz electrical stimulation in transfected hippocampal neurons and identified the phenotype of SpH-fluorescent synapses with post hoc immunostaining. With 200 stimuli (10 s), individual glutamate synapses displayed considerably more variability in peak SpH fluorescence than GABA synapses, without a strong difference in the mean SpH fluorescence increase. This spatial heterogeneity could not be accounted for by differences in endocytosis, which was nearly constant over these short time periods across glutamate and GABA synapses. Instead, variability in vesicle exocytosis correlated with variability in total vesicle staining and in measures of the total recycling pool size. Differences were also evident using FM1-43 [ N-(3-triethylammoniumpropyl)-4-(4-(dibutylamino)styryl) pyridinium dibromide] uptake. These data support the idea that the population of glutamate synapses exhibits more heterogeneity in release properties than the population of GABA synapses, possibly correlated with glutamatergic synaptic malleability.

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          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneuro
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          12 September 2007
          : 27
          : 37
          : 9846-9854
          Affiliations
          [1]Departments of 1Psychiatry and
          [2] 2Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110, and
          [3]Departments of 3Biological Engineering and
          [4] 4Medical Pharmacology and Physiology and the
          [5] 5Dalton Cardiovascular Research Center, University of Missouri–Columbia Research Park, Columbia, Missouri 65211
          Author notes
          Correspondence should be addressed to Dr. Krista Moulder, Department of Psychiatry, Washington University School of Medicine, 660 South Euclid Avenue, Box 8134, St. Louis, MO 63110. moulderk@ 123456psychiatry.wustl.edu
          Article
          PMC6672647 PMC6672647 6672647 3261170
          10.1523/JNEUROSCI.2803-07.2007
          6672647
          17855599
          bf5cd30a-ee3c-41da-961d-7868af04bddb
          Copyright © 2007 Society for Neuroscience 0270-6474/07/279846-09$15.00/0
          History
          : 16 March 2007
          : 18 July 2007
          : 21 July 2007
          Categories
          Articles
          Cellular/Molecular

          synaptic strength,transfection,synaptopHluorin,exocytosis,endocytosis,recycling pool

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