TY - JOUR
T1 - A stepwise neuron model fitting procedure designed for recordings with high spatial resolution
T2 - Application to layer 5 pyramidal cells
AU - Mäki-Marttunen, Tuomo
AU - Halnes, Geir
AU - Devor, Anna
AU - Metzner, Christoph
AU - Dale, Anders M.
AU - Andreassen, Ole A.
AU - Einevoll, Gaute T.
N1 - © 2017 The Author(s). Published by Elsevier B. V.
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence CC BY 4.0 (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Background Recent progress in electrophysiological and optical methods for neuronal recordings provides vast amounts of high-resolution data. In parallel, the development of computer technology has allowed simulation of ever-larger neuronal circuits. A challenge in taking advantage of these developments is the construction of single-cell and network models in a way that faithfully reproduces neuronal biophysics with subcellular level of details while keeping the simulation costs at an acceptable level. New method In this work, we develop and apply an automated, stepwise method for fitting a neuron model to data with fine spatial resolution, such as that achievable with voltage sensitive dyes (VSDs) and Ca2+ imaging. Result We apply our method to simulated data from layer 5 pyramidal cells (L5PCs) and construct a model with reduced neuronal morphology. We connect the reduced-morphology neurons into a network and validate against simulated data from a high-resolution L5PC network model. Comparison with existing methods Our approach combines features from several previously applied model-fitting strategies. The reduced-morphology neuron model obtained using our approach reliably reproduces the membrane-potential dynamics across the dendrites as predicted by the full-morphology model. Conclusions The network models produced using our method are cost-efficient and predict that interconnected L5PCs are able to amplify delta-range oscillatory inputs across a large range of network sizes and topologies, largely due to the medium after hyperpolarization mediated by the Ca2+-activated SK current.
AB - Background Recent progress in electrophysiological and optical methods for neuronal recordings provides vast amounts of high-resolution data. In parallel, the development of computer technology has allowed simulation of ever-larger neuronal circuits. A challenge in taking advantage of these developments is the construction of single-cell and network models in a way that faithfully reproduces neuronal biophysics with subcellular level of details while keeping the simulation costs at an acceptable level. New method In this work, we develop and apply an automated, stepwise method for fitting a neuron model to data with fine spatial resolution, such as that achievable with voltage sensitive dyes (VSDs) and Ca2+ imaging. Result We apply our method to simulated data from layer 5 pyramidal cells (L5PCs) and construct a model with reduced neuronal morphology. We connect the reduced-morphology neurons into a network and validate against simulated data from a high-resolution L5PC network model. Comparison with existing methods Our approach combines features from several previously applied model-fitting strategies. The reduced-morphology neuron model obtained using our approach reliably reproduces the membrane-potential dynamics across the dendrites as predicted by the full-morphology model. Conclusions The network models produced using our method are cost-efficient and predict that interconnected L5PCs are able to amplify delta-range oscillatory inputs across a large range of network sizes and topologies, largely due to the medium after hyperpolarization mediated by the Ca2+-activated SK current.
KW - Animals
KW - Automation, Laboratory/methods
KW - Calcium/metabolism
KW - Cerebral Cortex/cytology
KW - Computer Simulation
KW - Dendrites/physiology
KW - Image Processing, Computer-Assisted/methods
KW - Ion Channels/metabolism
KW - Membrane Potentials/physiology
KW - Models, Neurological
KW - Pattern Recognition, Automated
KW - Potassium/metabolism
KW - Pyramidal Cells/cytology
KW - Synapses/physiology
KW - Voltage-Sensitive Dye Imaging/methods
UR - http://www.scopus.com/inward/record.url?scp=85031754984&partnerID=8YFLogxK
U2 - 10.1016/j.jneumeth.2017.10.007
DO - 10.1016/j.jneumeth.2017.10.007
M3 - Article
AN - SCOPUS:85031754984
SN - 0165-0270
VL - 293
SP - 264
EP - 283
JO - Journal of Neuroscience Methods
JF - Journal of Neuroscience Methods
ER -