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Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI Research Institute for Particle and Nuclear Physics of the Hungarian Academy of Sciences, Dept. Biophysics 2 Institute for Psychology of the Hungarian Academy of Sciences 3 Center for Complex System Studies, Kalamazoo, Michigan, USA
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The aim: To determine the membrane currents on a single cell, based on extracellular data! The experimental setup: A 16 channel, extracellular (EC) electrode system is chronically implanted into cats primary auditory cortex: A1. The high-pass filtered raw data
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Mean spatio-temporal patterns of EC potential is obtained for each putative single neuron. The data we will work on: Mean spatio-temporal patterns of EC potential is obtained for each putative single neuron. StSpike clustering with Spike-o-matic.Cluster averages of 13 putative single cells.
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The EC potential is obtained from the transmembrane current source density via Poisson-equation, but the solution of the Poisson-inverse problem is generally non-unique. Infinitely many source distribution can generate the same measured EC potential distribution. The EC potential Ф=TJ, where J is the CSD and T is the lead-field matrix. The affine subspace of the possible solutions: J(x)=T + Ф+ker(T)x The problem
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The solution in theory From the multitude J(x) the proper solution can be chosen by applying a priory assumptions. In case of a single spike the proper assumptions are: 1, Each cell is a linesource, parallel to the electrode. 2, The spatial CSD distribution has a sharp negative peak (sink) at the soma, superposed onto a smooth positive (source) background. This assumption is shown to be valid during the first negative deflections of the EC spike. (Somogyvári et al. 2005)
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Requirement 1 can be incorporated into T. To comply the second requirement, the source with the sharpest peak should be chosen by founding the maximal projection of the theoretically sharpest distributions E i and the hyperplane T + Фker(T): max i (S)= max i (E i * (T + Фker(T))) The solution in theory II.
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The solution in work: The new spike-CSD method A mathematical “autofocus” algorithm results in not only the sharpest CSD picture, but an estimation for the distance of the cell.
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Tests on simulated data I. The sCSD outperforms the traditional CSD for these sources.
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Tests on simulated data II. The sCSD method reconstructs the original source with significantly smaller error than the traditional CSD, while provides an estimation about the cell-electrode distance also.
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Results I. Spatio-temporal dynamics of action potentials
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Results II. The sCSD method is able to uncover fine details and cell-type specific differences in initiation and spreading of action potentials, and even possible signs of Ranvier-nodes.
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Results III. Initiation of the action potential and the Ranvier-spikelets.
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Results IV. The speed of apical and basal backpropagation differs and signs of forward propagation also observed Two dimensional localization of neurons, results in realistic distances
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Results V. Henze et al. J. Neurphysiology 84 390-400 2000 Reconstruction of membrane potential, based on EC data with current-based compartmental model.
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The hope Identification of cortical synaptic input during paired- pulse experiments, could make possible to distinguish between changes in the network/connection s and in single cell response for the same input. Somewhere here, should be the input current, which cause the cell fire Thank You!
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