Skip to content
Licensed Unlicensed Requires Authentication Published by De Gruyter January 20, 2016

Putative duality of presynaptic events

  • Tatiana Borisova EMAIL logo and Arsenii Borysov

Abstract

The main structure in the brain responsible not only for nerve signal transmission but also for its simultaneous regulation is chemical synapse, where presynaptic nerve terminals are of considerable importance providing release of neurotransmitters. Analyzing transport of glutamate, the major excitatory neurotransmitter in the mammalian CNS, the authors suggest that there are two main relatively independent mechanisms at the presynaptic level that can influence the extracellular glutamate concentration, and so signaling, and its regulation. The first one is well-known precisely regulated compound exocytosis of synaptic vesicles containing neurotransmitters stimulated by membrane depolarization, which increases significantly glutamate concentration in the synaptic cleft and initiates glutamate signaling through postsynaptic glutamate receptors. The second one is permanent glutamate turnover across the plasma membrane that occurs without stimulation and is determined by simultaneous non-pathological transporter-mediated release of glutamate thermodynamically synchronized with uptake. Permanent glutamate turnover is responsible for maintenance of dynamic glutamatein/glutamateout gradient resulting in the establishment of a flexible extracellular level of glutamate, which can be unique for each synapse because of dependence on individual presynaptic parameters. These two mechanisms, i.e. exocytosis and transporter-mediated glutamate turnover, are both precisely regulated but do not directly interfere with each other, because they have different intracellular sources of glutamate in nerve terminals for release purposes, i.e. glutamate pool of synaptic vesicles and the cytoplasm, respectively. This duality can set up a presynaptic base for memory consolidation and storage, maintenance of neural circuits, long-term potentiation, and plasticity. Arguments against this suggestion are also considered.


Corresponding author: Tatiana Borisova, Palladin Institute of Biochemistry, Department of Neurochemistry, NAS of Ukraine, 9 Leontovicha Str, Kiev 01601, Ukraine, e-mail:

Acknowledgments

This work was supported by Science and Technology Center in Ukraine (STCU) project #6055 and Projects of National Academy of Sciences of Ukraine in the frame of the following programs: Scientific Space Research; ‘Molecular and cellular biotechnologies for medicine, industry and agriculture’; ‘Sensors for medicine, ecology, industry, and technology’; and Cedars Sinai Medical Center’s International Research and Innovation Management Program, the Association for Regional Cooperation in the Fields of Health, Science and Technology (RECOOP HST Association), and the participating Cedars–Sinai Medical Center–RECOOP Research Centers (CRRC).

Author’s disclosure statement: The authors declare no existing competing financial and personal interests.

References

Alabi, A.A. and Tsien, R.W. (2013). Perspectives on kiss-and-run: role in exocytosis, endocytosis, and neurotransmission. Annu. Rev. Physiol. 7, 393–422.10.1146/annurev-physiol-020911-153305Search in Google Scholar PubMed

Aliprandi, A., Longoni, M., Stanzani, L., Tremolizzo, L., Vaccaro, M., Begni, B., Galimberti, G., Garofolo, R., and Ferrarese, C. (2005). Increased plasma glutamate in stroke patients might be linked to altered platelet release and uptake. J. Cereb. Blood Flow Metab. 25, 513–519.10.1038/sj.jcbfm.9600039Search in Google Scholar PubMed

Amisten, S., Braun, O.O., Bengtsson, A., and Erlinge, D. (2008). Gene expression profiling for the identification of G-protein coupled receptors in human platelets. Thromb. Res. 122, 47–57.10.1016/j.thromres.2007.08.014Search in Google Scholar PubMed

Angulo, M.C., Kozlov, A.S., Charpak, S., and Audinat, E. (2004). Glutamate released from glial cells synchronizes neuronal activity in the hippocampus. J. Neurosci. 24, 6920–6927.10.1523/JNEUROSCI.0473-04.2004Search in Google Scholar PubMed PubMed Central

Baker, D.A., McFarland, K., Lake, R.W., Shen, H., Tang, X.C., Toda, S., and Kalivas, P.W. (2003). Neuroadaptations in cystine-glutamate exchange underlie cocaine relapse. Nat. Neurosci. 6, 743–749.10.1038/nn1069Search in Google Scholar PubMed

Borisova, T. (2013). Cholesterol and presynaptic glutamate transport in the brain (New York: Springer).10.1007/978-1-4614-7759-4Search in Google Scholar

Borisova T. (2016). Permanent dynamic transporter-mediated turnover of glutamate across the plasma membrane of presynaptic nerve terminals: arguments in favor and against. Rev. Neurosci. 27, 71–81.10.1515/revneuro-2015-0023Search in Google Scholar PubMed

Borisova, T. and Himmelreich, N. (2005). Centrifuge-induced hypergravity: [3H]GABA and L-[14C]glutamate uptake, exocytosis and efflux mediated by high-affinity, sodium-dependent transporters. Adv. Space Res. 36, 1340–1345.10.1016/j.asr.2005.10.007Search in Google Scholar

Borisova, T. and Krisanova N. (2008). Presynaptic transporter-mediated release of glutamate evoked by the protonophore FCCP increases under altered gravity conditions. Adv. Space. Res. 42, 1971–1979.10.1016/j.asr.2008.04.012Search in Google Scholar

Borisova, T., Krisanova, N., and Himmelreich, N. (2004). Exposure of animals to artificial gravity conditions leads to the alteration of the glutamate release from rat cerebral hemispheres nerve terminals. Adv. Space Res. 3, 1362–1367.10.1016/j.asr.2003.09.039Search in Google Scholar PubMed

Borisova, T., Krisanova, N., Sivko, R., and Borysov, A. (2010a). Cholesterol depletion attenuates tonic release but increases the ambient level of glutamate in rat brain synaptosomes. Neurochem. Int. 6, 466–478.10.1016/j.neuint.2009.12.006Search in Google Scholar

Borisova, T., Sivko, R., Borysov, A., and Krisanova, N. (2010b). Diverse presynaptic mechanisms underlying methyl-beta-cyclodextrin – mediated changes in glutamate transport. Cell. Mol. Neurobiol. 30, 1013–1023.10.1007/s10571-010-9532-xSearch in Google Scholar

Borisova, T., Nazarova, A., Dekaliuk, M., Krisanova, N., Pozdnyakova, N., Borysov, A., Sivko, R., and Demchenko, A.P. (2015). Neuromodulatory properties of fluorescent carbon dots: Effect on exocytotic release, uptake and ambient level of glutamate and GABA in brain nerve terminals. Int. J. Biochem. Cell Biol. 59, 203–215.10.1016/j.biocel.2014.11.016Search in Google Scholar

Bridges, R.J., Natale, N.R., and Patel, S.A. (2012). System xc cystine/glutamate antiporter: an update on molecular pharmacology and roles within the CNS. Br. J. Pharmacol. 165, 20–34.10.1111/j.1476-5381.2011.01480.xSearch in Google Scholar

Cavelier, P. and Attwell, D.L. (2005). Tonic release of glutamate by a DIDS-sensitive mechanism in rat hippocampal slices. J. Physiol. 564, 397–410.10.1113/jphysiol.2004.082131Search in Google Scholar

Cavelier, P., Hamann, M., Rossi, D., Mobbs, P., and Attwell, D. (2005). Tonic excitation and inhibition of neurons: ambient transmitter sources and computational consequences. Prog. Biophys. Mol. Biol. 87, 3–16.10.1016/j.pbiomolbio.2004.06.001Search in Google Scholar

Dalby, N.O. and Mody, I. (2003). Activation of NMDA receptors in rat dentate gyrus granule cells by spontaneous and evoked transmitter release. J. Neurophysiol. 90, 786–797.10.1152/jn.00118.2003Search in Google Scholar

Danbolt, N.C. (2001). Glutamate uptake. Prog. Neurobiol. 65, 1–105.10.1016/S0301-0082(00)00067-8Search in Google Scholar

Divino Filho, J.C., Hazel, S.J., Furst, P., Bergstrom, J., and Hall, K. (1998). Glutamate concentration in plasma, erythrocyte and muscle in relation to plasma levels of insulin-like growth factor (IGF)-I, IGF binding protein-1 and insulin in patients on haemodialysis. J. Endocrinol. 156, 519–527.10.1677/joe.0.1560519Search in Google Scholar PubMed

Dzubay, J.A. and Jahr, C.E. (1999). The concentration of synaptically released glutamate outside of the climbing fiber-Purkinje cell synaptic cleft. J. Neurosci. 19, 5265–5274.10.1523/JNEUROSCI.19-13-05265.1999Search in Google Scholar

Farrant, M. and Nusser, Z. (2005). Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors. Nat. Rev. Neurosci. 6, 215–229.10.1038/nrn1625Search in Google Scholar PubMed

Featherstone, D.E. and Shippy, S.A. (2008). Regulation of synaptic transmission by ambient extracellular glutamate. Neuroscientist 14, 171–181.10.1177/1073858407308518Search in Google Scholar PubMed PubMed Central

González, M.I., Kazanietz, M.G., and Robinson, M.B. (2002). Regulation of the neuronal glutamate transporter excitatory amino acid carrier-1 (EAAC1) by different protein kinase C subtypes. Mol. Pharmacol. 62, 901–910.10.1124/mol.62.4.901Search in Google Scholar PubMed

Grewer, C., Gameiro, A., Zhang Z., Tao, Z., Braams, S., and Rauen, T. (2008). Glutamate forward and reverse transport: From molecular mechanism to transporter-mediated release after ischemia. IUBMB Life 60, 609–619.10.1002/iub.98Search in Google Scholar PubMed PubMed Central

Herman, M.A. and Jahr, C.E. (2007). Extracellular glutamate concentration in hippocampal slice. J. Neurosci. 27, 9736–9741.10.1523/JNEUROSCI.3009-07.2007Search in Google Scholar PubMed PubMed Central

Jabaudon, D., Shimamoto, K., and Yasuda-Kamatani, Y. (1999). Inhibition of uptake unmasks rapid extracellular turnover of glutamate of nonvesicular origin. Proc. Natl. Acad. Sci. USA 96, 8733–8738.10.1073/pnas.96.15.8733Search in Google Scholar PubMed PubMed Central

Kasatkina, L. and Borisova, T. (2013). Glutamate release from platelets: exocytosis versus glutamate transporter reversal. Int. J. Biochem. Cell Biol. 45, 2585–2595.10.1016/j.biocel.2013.08.004Search in Google Scholar PubMed

Kavalali, E.T. (2015). The mechanisms and functions of spontaneous neurotransmitter release. Nat. Rev. Neurosci 16, 5–16.10.1038/nrn3875Search in Google Scholar PubMed

Le Meur, K., Galante, M., Angulo, M.C., and Audinat, E. (2007). Tonic activation of NMDA receptors by ambient glutamate of non-synaptic origin in the rat hippocampus. J. Physiol. 580, 373–383.10.1113/jphysiol.2006.123570Search in Google Scholar PubMed PubMed Central

Makarov, V., Kucheryavykh, L., Kucheryavykh, Y., Rivera, A., Eaton, M.J., Skatchkov, S.N., and Inyushin, M. (2013). Transport reversal during heteroexchange: A kinetic study J. Biophys. 2013, 683256.10.1155/2013/683256Search in Google Scholar PubMed PubMed Central

Mayford, M., Siegelbaum, S.A., Kandel, E.R. (2012). Synapses and memory storage. Cold Spring Harb. Perspect. Biol. 4, a005751.10.1101/cshperspect.a005751Search in Google Scholar PubMed PubMed Central

Moser, M-B., Rowland, D.C, Moser E.I. (2015). Place cells, grid cells, and memory. Cold Spring Harb. Perspect. Biol. 7, a021808.10.1101/cshperspect.a021808Search in Google Scholar PubMed PubMed Central

Moussawi, K., Riegel, A., Nair, S., and Kalivas, P.W. (2011). Extracellular glutamate: Functional compartments operate in different concentration ranges. Front. Syst. Neurosci. 5, 94.10.3389/fnsys.2011.00094Search in Google Scholar PubMed PubMed Central

Murphy-Royal, C., Dupuis, J.P., Varela, J.A., Panatier, A., Pinson, B., Baufreton, J., Groc, L., and Oliet, S.H.R. (2015). Surface diffusion of astrocytic glutamate transporters shapes synaptic transmission. Nat. Neurosci. 18, 219–228.10.1038/nn.3901Search in Google Scholar PubMed

Pendyam, S., Mohan, A., Kalivas, P.W., and Nair, S.S. (2012). Role of perisynaptic parameters in neurotransmitter homeostasis – computational study of a general synapse. Synapse 66, 608–621.10.1002/syn.21547Search in Google Scholar PubMed PubMed Central

Pozdnyakova, N., Dudarenko, M., Yatsenko, L., Himmelreich, N., Krupko, O., and Borisova, T. (2014). Perinatal hypoxia: different effects of the inhibitors of GABA transporters GAT-1 and GAT-3 on the initial velocity of [3H]GABA uptake by cortical, hippocampal and thalamic nerve terminals. Croat. Med. J. 55, 250–258.10.3325/cmj.2014.55.250Search in Google Scholar PubMed PubMed Central

Rizzoli, S.O. (2014). Synaptic vesicle recycling: steps and principles. EMBO J. 33, 788–822.10.1002/embj.201386357Search in Google Scholar PubMed PubMed Central

Sah, P., Hestrin, S., and Nicoll, R.A. (1989). Tonic activation of NMDA receptors by ambient glutamate enhances excitability of neurons. Science 246, 815–818.10.1126/science.2573153Search in Google Scholar PubMed

Semyanov, A., Walker, M.C., Kullmann, D.M., and Silver, R.A. (2004). Tonically active GABAAreceptors: modulating gain and maintaining the tone. Trends Neurosci. 27, 262–269.10.1016/j.tins.2004.03.005Search in Google Scholar PubMed

Soldatkin, O., Nazarova, A., Krisanova, N., Borysov, A., Kucherenko, D., Kucherenko, I., Pozdnyakova, N., Soldatkin, A., and Borisova T. (2015). Monitoring of the velocity of high-affinity glutamate uptake by isolated brain nerve terminals using amperometric glutamate biosensor. Talanta. 135, 67–74.10.1016/j.talanta.2014.12.031Search in Google Scholar PubMed

Sudhof, T.C. (2004). The synaptic vesicle cycle. Annu. Rev. Neurosci. 27, 509–547.10.1146/annurev.neuro.26.041002.131412Search in Google Scholar

Sun, H., Swaim, A., Herrera, J.E., Becker, D., Becker, L., Srivastava, K., Thompson, L.E., Shero, M.R., Perez-Tamayo, A., Suktitipat, B., et al. (2009). Platelet kainate receptor signaling promotes thrombosis by stimulating cyclooxygenase activation. Circ. Res. 105, 595–603.10.1161/CIRCRESAHA.109.198861Search in Google Scholar

Truckenbrodt, S. and Rizzoli, S.O. (2014). Spontaneous vesicle recycling in the synaptic bouton. Front. Cell. Neurosci. 8, 409.10.3389/fncel.2014.00409Search in Google Scholar

Watzke, N. and Grewer, C. (2001). The anion conductance of the glutamate transporter EAAC1 depends on the direction of glutamate transport. FEBS Lett. 503, 121–125.10.1016/S0014-5793(01)02715-6Search in Google Scholar

Van der Zeyden, M., Oldenziel, W.H., Rea, K., Cremers, T.I., and Westerink, B.H. (2008). Microdialysis of GABA and glutamate: analysis, interpretation and comparison with microsensors. Pharmacol. Biochem. Behav. 90, 135–147.10.1016/j.pbb.2007.09.004Search in Google Scholar PubMed

Received: 2015-8-28
Accepted: 2015-11-13
Published Online: 2016-1-20
Published in Print: 2016-6-1

©2016 by De Gruyter

Downloaded on 30.5.2024 from https://www.degruyter.com/document/doi/10.1515/revneuro-2015-0044/html
Scroll to top button