4.8 Article

Metaplasticity at CA1 Synapses by Homeostatic Control of Presynaptic Release Dynamics

Journal

CELL REPORTS
Volume 21, Issue 5, Pages 1293-1303

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2017.10.025

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Funding

  1. Government of Ontario
  2. Canadian Institutes of Health Research
  3. Canadian Institutes of Health Research [MOP 115061]
  4. Natural Sciences and Engineering Research Council of Canada [RGPIN/ 2015-05830]
  5. Canada Foundation for Innovation [CFI 23915]
  6. Heart and Stroke Foundation's Canadian Partnership for Stroke Recovery, Brain Canada (Canadian Neurophotonic Platform)
  7. University of Ottawa's Brain and Mind Research Institute

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Hebbian and homeostatic forms of plasticity operate on different timescales to regulate synaptic strength. The degree of mechanistic overlap between these processes and their mutual influence are still incompletely understood. Here, we report that homeostatic synaptic strengthening induced by prolonged network inactivity compromised the ability of CA1 synapses to exhibit LTP. This effect could not be accounted for by an obvious deficit in the postsynaptic capacity for LTP expression, since neither the fraction of silent synapses nor the ability to induce LTP by two-photon glutamate uncaging were reduced by the homeostatic process. Rather, optical quantal analysis reveals that homeostatically strengthened synapses display a reduced capacity to maintain glutamate release fidelity during repetitive stimulation, ultimately impeding the induction, and thus expression, of LTP. By regulating the short-term dynamics of glutamate release, the homeostatic process thus influences key aspects of dynamic network function and exhibits features of metaplasticity.

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