5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Rapid and sustained homeostatic control of presynaptic exocytosis at a central synapse

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Significance

          Homeostatic mechanisms stabilize neural activity, and there are genetic links between homeostatic plasticity and neural disease. While homeostatic plasticity in the central nervous system (CNS) operates on relatively slow time scales of hours to days, activity-dependent forms of synaptic plasticity alter neural activity on much faster time scales. It is unclear if homeostatic plasticity stabilizes CNS synapses on rapid time scales. Here, we uncovered that cerebellar synapses stabilize transmission within minutes upon activity perturbation. This is achieved through homeostatic control of presynaptic exocytosis. We show that synergistic modulation of distinct presynaptic mechanisms not only maintains synaptic efficacy on rapid, but also on prolonged time scales. Homeostatic control of presynaptic exocytosis may be a general mechanism for stabilizing CNS function.

          Abstract

          Animal behavior is remarkably robust despite constant changes in neural activity. Homeostatic plasticity stabilizes central nervous system (CNS) function on time scales of hours to days. If and how CNS function is stabilized on more rapid time scales remains unknown. Here, we discovered that mossy fiber synapses in the mouse cerebellum homeostatically control synaptic efficacy within minutes after pharmacological glutamate receptor impairment. This rapid form of homeostatic plasticity is expressed presynaptically. We show that modulations of readily releasable vesicle pool size and release probability normalize synaptic strength in a hierarchical fashion upon acute pharmacological and prolonged genetic receptor perturbation. Presynaptic membrane capacitance measurements directly demonstrate regulation of vesicle pool size upon receptor impairment. Moreover, presynaptic voltage-clamp analysis revealed increased Ca 2+-current density under specific experimental conditions. Thus, homeostatic modulation of presynaptic exocytosis through specific mechanisms stabilizes synaptic transmission in a CNS circuit on time scales ranging from minutes to months. Rapid presynaptic homeostatic plasticity may ensure stable neural circuit function in light of rapid activity-dependent plasticity.

          Related collections

          Most cited references43

          • Record: found
          • Abstract: found
          • Article: not found

          The self-tuning neuron: synaptic scaling of excitatory synapses.

          Homeostatic synaptic scaling is a form of synaptic plasticity that adjusts the strength of all of a neuron's excitatory synapses up or down to stabilize firing. Current evidence suggests that neurons detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites. Additional mechanisms may allow local or network-wide changes in activity to be sensed through parallel pathways, generating a nested set of homeostatic mechanisms that operate over different temporal and spatial scales.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Variability, compensation and homeostasis in neuron and network function.

            Neurons in most animals live a very long time relative to the half-lives of all of the proteins that govern excitability and synaptic transmission. Consequently, homeostatic mechanisms are necessary to ensure stable neuronal and network function over an animal's lifetime. To understand how these homeostatic mechanisms might function, it is crucial to understand how tightly regulated synaptic and intrinsic properties must be for adequate network performance, and the extent to which compensatory mechanisms allow for multiple solutions to the production of similar behaviour. Here, we use examples from theoretical and experimental studies of invertebrates and vertebrates to explore several issues relevant to understanding the precision of tuning of synaptic and intrinsic currents for the operation of functional neuronal circuits.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Unraveling mechanisms of homeostatic synaptic plasticity.

              Homeostatic synaptic plasticity is a negative feedback mechanism that neurons use to offset excessive excitation or inhibition by adjusting their synaptic strengths. Recent findings reveal a complex web of signaling processes involved in this compensatory form of synaptic strength regulation, and in contrast to the popular view of homeostatic plasticity as a slow, global phenomenon, neurons may also rapidly tune the efficacy of individual synapses on demand. Here we review our current understanding of cellular and molecular mechanisms of homeostatic synaptic plasticity. Copyright 2010 Elsevier Inc. All rights reserved.
                Bookmark

                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                19 November 2019
                4 November 2019
                4 November 2019
                : 116
                : 47
                : 23783-23789
                Affiliations
                [1] aInstitute of Molecular Life Sciences, University of Zurich , 8057 Zurich, Switzerland;
                [2] bNeuroscience Center Zurich , University of Zurich, ETH Zurich, 8057 Zurich, Switzerland
                Author notes
                1To whom correspondence may be addressed. Email: martin.mueller@ 123456imls.uzh.ch .

                Edited by Reinhard Jahn, Max Planck Institute for Biophysical Chemistry, Goettingen, Germany, and approved October 10, 2019 (received for review June 6, 2019)

                Author contributions: I.D. and M.M. designed research; I.D. and K.K. performed research; I.D. and K.K. analyzed data; and I.D. and M.M. wrote the paper.

                Author information
                http://orcid.org/0000-0002-6151-2363
                http://orcid.org/0000-0003-1624-6761
                Article
                201909675
                10.1073/pnas.1909675116
                6876255
                31685637
                99be7102-5a01-45d7-ace0-ebddc4a2959b
                Copyright © 2019 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).

                History
                Page count
                Pages: 7
                Funding
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 501100001711
                Award ID: PP00P3_144816
                Award Recipient : Igor Delvendahl Award Recipient : Martin Müller
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 501100001711
                Award ID: PZ00P3_174018
                Award Recipient : Igor Delvendahl Award Recipient : Martin Müller
                Funded by: EC | H2020 | H2020 Priority Excellent Science | H2020 European Research Council (ERC) 100010663
                Award ID: 679881 'Syndegrade'
                Award Recipient : Martin Müller
                Categories
                Biological Sciences
                Neuroscience

                homeostatic plasticity,synaptic transmission,exocytosis,mossy fiber,cerebellum

                Comments

                Comment on this article