Competition between phasic and asynchronous release for recovered synaptic vesicles at developing hippocampal autaptic synapses

Otsu, Y., Shahrezaei, V., Li, B., Raymond, L. A., Delaney, K. R., Murphy, T. H. (January 2004) Competition between phasic and asynchronous release for recovered synaptic vesicles at developing hippocampal autaptic synapses. Journal of Neuroscience, 24 (2). pp. 420-33. ISSN 0270-6474

[img]
Preview
PDF (Paper)
Li J Neuroscience 2004.pdf - Published Version

Download (559Kb) | Preview
URL: http://www.ncbi.nlm.nih.gov/pubmed/14724240
DOI: 10.1523/jneurosci.4452-03.2004

Abstract

Developing hippocampal neurons in microisland culture undergo rapid and extensive transmitter release-dependent depression of evoked (phasic) excitatory synaptic activity in response to 1 sec trains of 20 Hz stimulation. Although evoked phasic release was attenuated by repeated stimuli, asynchronous (miniature like) release continued at a high rate equivalent to approximately 2.8 readily releasable pools (RRPs) of quanta/sec. Asynchronous release reflected the recovery and immediate release of quanta because it was resistant to sucrose-induced depletion of the RRP. Asynchronous and phasic release appeared to compete for a common limited supply of release-ready quanta because agents that block asynchronous release, such as EGTA-AM, led to enhanced steady-state phasic release, whereas prolongation of the asynchronous release time course by LiCl delayed recovery of phasic release from depression. Modeling suggested that the resistance of asynchronous release to depression was associated with its ability to out-compete phasic release for recovered quanta attributable to its relatively low release rate (up to 0.04/msec per vesicle) stimulated by bulk intracellular Ca2+ concentration ([Ca2+]i) that could function over prolonged intervals between successive stimuli. Although phasic release was associated with a considerably higher peak rate of release (0.4/msec per vesicle), the [Ca2+]i microdomains that trigger it are brief (1 msec), and with asynchronous release present, relatively few quanta can accumulate within the RRP to be available for phasic release. We conclude that despite depression of phasic release during train stimulation, transmission can be maintained at a near-maximal rate by switching to an asynchronous mode that takes advantage of a bulk presynaptic [Ca2+]i.

Item Type: Paper
Uncontrolled Keywords: Animals Cells, Cultured Excitatory Postsynaptic Potentials Hippocampus/growth & development/*physiology Kinetics Long-Term Synaptic Depression Models, Neurological Patch-Clamp Techniques Periodicity Pyramidal Cells/metabolism/physiology Rats Synapses/metabolism/*physiology *Synaptic Transmission Synaptic Vesicles/*metabolism
Subjects: organs, tissues, organelles, cell types and functions > tissues types and functions > hippocampus
organs, tissues, organelles, cell types and functions > sub-cellular tissues: types and functions > synapse
organs, tissues, organelles, cell types and functions > cell types and functions > cell functions > synaptic transmission
CSHL Authors:
Communities: CSHL labs > Li lab
Depositing User: Matt Covey
Date: 14 January 2004
Date Deposited: 12 Dec 2014 16:01
Last Modified: 12 Dec 2014 16:01
Related URLs:
URI: http://repository.cshl.edu/id/eprint/30964

Actions (login required)

Administrator's edit/view item Administrator's edit/view item
CSHL HomeAbout CSHLResearchEducationNews & FeaturesCampus & Public EventsCareersGiving