Inverse solutions for localization of single cell currents based on extracellular measurements...

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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

Transcript of Inverse solutions for localization of single cell currents based on extracellular measurements...

Page 1: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

Inverse solutions for localization of single cell currents based on extracellular measurements

Zoltán Somogyvári1, István Ulbert2, Péter Érdi1,3

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 Sciences3 Center for Complex System Studies, Kalamazoo, Michigan, USA

Page 2: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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

Page 3: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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.

Page 4: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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

Page 5: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

The solution in theoryFrom 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)

Page 6: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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+Ф⨯ker(T):

maxi (S)=

max

i(E

i*

(T+Ф⨯ker(T)))

The solution in theory II.

Page 7: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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.

Page 8: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

Tests on simulated data I.

The sCSD outperforms the traditional CSD for these sources.

Page 9: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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.

Page 10: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

Results I.

Spatio-temporal dynamics of action potentials

Page 11: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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.

Page 12: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

Results III.

Initiation of the action potential and the Ranvier-spikelets.

Page 13: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

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

Page 14: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

Results V.

Henze et al. J. Neurphysiology 84 390-400 2000

Reconstruction of membrane potential, based on EC data with current-based compartmental model.

Page 15: Inverse solutions for localization of single cell currents based on extracellular measurements Zoltán Somogyvári 1, István Ulbert 2, Péter Érdi 1,3 1 KFKI.

The hope

Identification of cortical synaptic input during paired-pulse experiments, could make possible to distinguish between changes in the network/connections and in single cell response for the same input.

Somewhere here,should be the input current,which cause the cell fire

Thank You!