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The Glutamatergic Synapse: a Complex Machinery for Information Processing

Overview
Journal Cogn Neurodyn
Publisher Springer
Specialty Neurology
Date 2021 Oct 4
PMID 34603541
Citations 13
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Abstract

Being the most abundant synaptic type, the glutamatergic synapse is responsible for the larger part of the brain's information processing. Despite the conceptual simplicity of the basic mechanism of synaptic transmission, the glutamatergic synapse shows a large variation in the response to the presynaptic release of the neurotransmitter. This variability is observed not only among different synapses but also in the same single synapse. The synaptic response variability is due to several mechanisms of control of the information transferred among the neurons and suggests that the glutamatergic synapse is not a simple bridge for the transfer of information but plays an important role in its elaboration and management. The control of the synaptic information is operated at pre, post, and extrasynaptic sites in a sort of cooperation between the pre and postsynaptic neurons which also involves the activity of other neurons. The interaction between the different mechanisms of control is extremely complicated and its complete functionality is far from being fully understood. The present review, although not exhaustively, is intended to outline the most important of these mechanisms and their complexity, the understanding of which will be among the most intriguing challenges of future neuroscience.

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References
1.
KOESTER H, Sakmann B . Calcium dynamics in single spines during coincident pre- and postsynaptic activity depend on relative timing of back-propagating action potentials and subthreshold excitatory postsynaptic potentials. Proc Natl Acad Sci U S A. 1998; 95(16):9596-601. PMC: 21384. DOI: 10.1073/pnas.95.16.9596. View

2.
De Pitta M, Volman V, Berry H, Parpura V, Volterra A, Ben-Jacob E . Computational quest for understanding the role of astrocyte signaling in synaptic transmission and plasticity. Front Comput Neurosci. 2012; 6:98. PMC: 3528083. DOI: 10.3389/fncom.2012.00098. View

3.
Sabatini B, Svoboda K . Analysis of calcium channels in single spines using optical fluctuation analysis. Nature. 2000; 408(6812):589-93. DOI: 10.1038/35046076. View

4.
Lu W, Man H, Ju W, Trimble W, MacDonald J, Wang Y . Activation of synaptic NMDA receptors induces membrane insertion of new AMPA receptors and LTP in cultured hippocampal neurons. Neuron. 2001; 29(1):243-54. DOI: 10.1016/s0896-6273(01)00194-5. View

5.
Clements J, Feltz A, Sahara Y, Westbrook G . Activation kinetics of AMPA receptor channels reveal the number of functional agonist binding sites. J Neurosci. 1998; 18(1):119-27. PMC: 6793380. View