Glutamate released from glial cells synchronizes neuronal activity in the hippocampus.

@article{Angulo2004, abstract = {Glial cells of the nervous system directly influence neuronal and synaptic activities by releasing transmitters. However, the physiological consequences of this glial transmitter release on brain information processing remain poorly understood. We demonstrate here in hippocampal slices of 2- to 5-week-old rats that glutamate released from glial cells generates slow transient currents (STCs) mediated by the activation of NMDA receptors in pyramidal cells. STCs persist in the absence of neuronal and synaptic activity, indicating a nonsynaptic origin of the source of glutamate. Indeed, STCs occur spontaneously but can also be induced by pharmacological tools known to activate astrocytes and by the selective mechanical stimulation of single nearby glial cells. Bath application of the inhibitor of the glutamate uptake dl-threo-beta-benzyloxyaspartate increases both the frequency of STCs and the amplitude of a tonic conductance mediated by NMDA receptors and probably also originated from glial glutamate release. By using dual recordings, we observed synchronized STCs in pyramidal cells having their soma distant by <100 microm. The degree of precision (<100 msec) of this synchronization rules out the involvement of calcium waves spreading through the glial network. It also indicates that single glial cells release glutamate onto adjacent neuronal processes, thereby controlling simultaneously the excitability of several neighboring pyramidal cells. In conclusion, our results show that the glial glutamate release occurs spontaneously and synchronizes the neuronal activity in the hippocampus.}, address = {Laboratoire de Neurophysiologie et Nouvelles Microscopies, Institut National de la Sant\'{e} et de la Recherche M\'{e}dicale U603, Centre National de la Recherche Scientifique FRE 2500, Ecole Sup\'{e}rieure de Physique et Chimie Industrielles, 75005 Paris, France.}, author = {Angulo, M. C. and Kozlov, A. S. and Charpak, S. and Audinat, E. }, citeulike-article-id = {2672736}, doi = {10.1523/JNEUROSCI.0473-04.2004}, issn = {1529-2401}, journal = {The Journal of neuroscience : the official journal of the Society for Neuroscience}, keywords = {glial, hippocampus}, month = {August}, number = {31}, pages = {6920--6927}, posted-at = {2008-04-15 10:53:18}, priority = {2}, title = {Glutamate released from glial cells synchronizes neuronal activity in the hippocampus.}, url = {http://dx.doi.org/10.1523/JNEUROSCI.0473-04.2004}, volume = {24}, year = {2004} }

TY - JOUR ID - Angulo2004 L3 - citeulike-article-id:2672736 TI - Glutamate released from glial cells synchronizes neuronal activity in the hippocampus. JF - The Journal of neuroscience : the official journal of the Society for Neuroscience VL - 24 IS - 31 SP - 6920 EP - 6927 AD - Laboratoire de Neurophysiologie et Nouvelles Microscopies, Institut National de la Santé et de la Recherche Médicale U603, Centre National de la Recherche Scientifique FRE 2500, Ecole Supérieure de Physique et Chimie Industrielles, 75005 Paris, France. SN - 1529-2401 N2 - Glial cells of the nervous system directly influence neuronal and synaptic activities by releasing transmitters. However, the physiological consequences of this glial transmitter release on brain information processing remain poorly understood. We demonstrate here in hippocampal slices of 2- to 5-week-old rats that glutamate released from glial cells generates slow transient currents (STCs) mediated by the activation of NMDA receptors in pyramidal cells. STCs persist in the absence of neuronal and synaptic activity, indicating a nonsynaptic origin of the source of glutamate. Indeed, STCs occur spontaneously but can also be induced by pharmacological tools known to activate astrocytes and by the selective mechanical stimulation of single nearby glial cells. Bath application of the inhibitor of the glutamate uptake dl-threo-beta-benzyloxyaspartate increases both the frequency of STCs and the amplitude of a tonic conductance mediated by NMDA receptors and probably also originated from glial glutamate release. By using dual recordings, we observed synchronized STCs in pyramidal cells having their soma distant by <100 microm. The degree of precision (<100 msec) of this synchronization rules out the involvement of calcium waves spreading through the glial network. It also indicates that single glial cells release glutamate onto adjacent neuronal processes, thereby controlling simultaneously the excitability of several neighboring pyramidal cells. In conclusion, our results show that the glial glutamate release occurs spontaneously and synchronizes the neuronal activity in the hippocampus. KW - glial KW - hippocampus AU - Angulo, MC AU - Kozlov, AS AU - Charpak, S AU - Audinat, E PY - 2004/08/04/ UR - http://dx.doi.org/10.1523/JNEUROSCI.0473-04.2004 ER -