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- Open Access
A computational study of the influence of synaptic cooperativity on synaptic plasticity in a hippocampal CA1 pyramidal cell
© Graham et al; licensee BioMed Central Ltd. 2012
- Published: 16 July 2012
- Pyramidal Cell
- Calcium Entry
- Apical Dendrite
- Stratum Radiatum
- Peak Calcium
We use a computational model to investigate the possible cooperativity between coactive synapses, both within and between input pathways, in determining plasticity outcomes at individual synapses on a hippocampal CA1 pyramidal cell (PC). The detailed compartmental model of the PC, based on a reconstructed morphology, contains distributions of core ion channels that control voltage transients and calcium entry in the soma and dendrites. Of particular note are the increasing density of A-type potassium channels (KA) with distance in the apical dendrites that provide strong filtering of voltage transients, and high-voltage-gated calcium channels (VGCC) in the dendrites and spines that may contribute to calcium entry in spine heads. Groups of spatially diffuse or clustered excitatory synapses on spines in dendritic layers stratum lacunosum-moleculare (SLM), stratum radiatum (SR) and stratum oriens (SO) are stimulated with single spikes or high frequency bursts. Synaptic currents are mediated by AMPA and NMDA receptors. A proportion of the NMDAR-mediated current is carried by calcium ions. As an indicator of likely synaptic plasticity, the peak calcium level (pCa) obtained in each spine head is measured.
Other results show that presynaptic burst stimulation is much more effective at raising spine head calcium levels than single stimuli. Similarly, small numbers of coactive synapses on a single oblique dendrite can achieve high pCa. Activity in one layer, such as SLM can affect pCa in another layer (SR) but only if KA is reduced.
In summary, burst stimulation and colocalised activity are most likely to lead to high pCa and hence LTP. Cooperativity across dendritic pathways is possible, but needs specific cellular and stimulation conditions.
AS acknowledges funding from the Research Council of Lithuania.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.