|Appears in Collections:||Computing Science and Mathematics Journal Articles|
|Peer Review Status:||Unrefereed|
|Title:||Spine head calcium as a measure of summed postsynaptic activity for driving synaptic plasticity|
Cobb, Stuart R
|Citation:||Graham B, Saudargiene A & Cobb SR (2014) Spine head calcium as a measure of summed postsynaptic activity for driving synaptic plasticity. Neural Computation, 26 (10), pp. 2194-2222. https://doi.org/10.1162/NECO_a_00640|
|Abstract:||We use a computational model of a hippocampal CA1 pyramidal cell to demonstrate that spine head calcium provides an instantaneous readout at each synapse of the postsynaptic weighted sum of all presynaptic activity impinging on the cell. The form of the readout is equivalent to the functions of weighted, summed inputs used in neural network learning rules. Within a dendritic layer, peak spine head calcium levels are either a linear or sigmoidal function of the number of coactive synapses, with nonlinearity depending on the ability of voltage spread in the dendrites to reach calcium spike threshold. This is strongly controlled by the potassium A-type current, with calcium spikes and the consequent sigmoidal increase in peak spine head calcium present only when the A-channel density is low. Other membrane characteristics influence the gain of the relationship between peak calcium and the number of active synapses. In particular, increasing spine neck resistance increases the gain due to increased voltage responses to synaptic input in spine heads. Colocation of stimulated synapses on a single dendritic branch also increases the gain of the response. Input pathways cooperate: CA3 inputs to the proximal apical dendrites can strongly amplify peak calcium levels due to weak EC input to the distal dendrites, but not so strongly vice versa. CA3 inputs to the basal dendrites can boost calcium levels in the proximal apical dendrites, but the relative electrical compactness of the basal dendrites results in the reverse effect being less significant. These results give pointers as to how to better describe the contributions of pre- and postsynaptic activity in the learning "rules" that apply in these cells. The calcium signal is closer in form to the activity measures used in traditional neural network learning rules than to the spike times used in spike-timing-dependent plasticity.|
|Rights:||This item has been embargoed for a period. During the embargo please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study. Publisher policy allows this work to be made available in this repository. Published in Neural Computation, October 2014, Vol. 26, No. 10, Pages 2194-2222 by MIT Press. The original publication is available at: http://www.mitpressjournals.org/doi/abs/10.1162/NECO_a_00640|
|Notes:||Output Type: Letter|
|NECO_a_00640.pdf||Fulltext - Published Version||590.58 kB||Adobe PDF||View/Open|
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