Orientation preference in L23 V1 pyramidal neurons (Park et al 2019)

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"Pyramidal neurons integrate synaptic inputs from basal and apical dendrites to generate stimulus-specific responses. It has been proposed that feed-forward inputs to basal dendrites drive a neuron’s stimulus preference, while feedback inputs to apical dendrites sharpen selectivity. However, how a neuron’s dendritic domains relate to its functional selectivity has not been demonstrated experimentally. We performed 2-photon dendritic micro-dissection on layer-2/3 pyramidal neurons in mouse primary visual cortex. We found that removing the apical dendritic tuft did not alter orientation-tuning. Furthermore, orientation-tuning curves were remarkably robust to the removal of basal dendrites: ablation of 2 basal dendrites was needed to cause a small shift in orientation preference, without significantly altering tuning width. Computational modeling corroborated our results and put limits on how orientation preferences among basal dendrites differ in order to reproduce the post-ablation data. In conclusion, neuronal orientation-tuning appears remarkably robust to loss of dendritic input."
1 . Park J, Papoutsi A, Ash RT, Marin MA, Poirazi P, Smirnakis SM (2019) Contribution of apical and basal dendrites to orientation encoding in mouse V1 L2/3 pyramidal neurons Nature Communications 10:5372
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Model Information (Click on a link to find other models with that property)
Model Type:
Brain Region(s)/Organism: Neocortex;
Cell Type(s): Neocortex L2/3 pyramidal GLU cell;
Channel(s): I L high threshold; I T low threshold; I A; I K,Ca; I M; I K; I Na,t;
Gap Junctions:
Receptor(s): GabaA; NMDA; AMPA;
Transmitter(s): Gaba; Glutamate;
Simulation Environment: NEURON;
Model Concept(s): Vision;
Implementer(s): Papoutsi, Athanasia [athpapoutsi at gmail.com];
Search NeuronDB for information about:  Neocortex L2/3 pyramidal GLU cell; GabaA; AMPA; NMDA; I Na,t; I L high threshold; I T low threshold; I A; I K; I M; I K,Ca; Gaba; Glutamate;
:26 Ago 2002 Modification of original channel to allow variable time step and to correct an initialization error.
:    Done by Michael Hines(michael.hines@yale.e) and Ruggero Scorcioni(rscorcio@gmu.edu) at EU Advance Course in Computational Neuroscience. Obidos, Portugal

TITLE decay of internal calcium concentration
: Internal calcium concentration due to calcium currents and pump.
: Differential equations.
: Simple model of ATPase pump with 3 kinetic constants (Destexhe 92)
:     Cai + P <-> CaP -> Cao + P  (k1,k2,k3)
: A Michaelis-Menten approximation is assumed, which reduces the complexity
: of the system to 2 parameters: 
:       kt = <tot enzyme concentration> * k3  -> TIME CONSTANT OF THE PUMP
:	kd = k2/k1 (dissociation constant)    -> EQUILIBRIUM CALCIUM VALUE
: The values of these parameters are chosen assuming a high affinity of 
: the pump to calcium and a low transport capacity (cfr. Blaustein, 
: TINS, 11: 438, 1988, and references therein).  
: Units checked using "modlunit" -> factor 10000 needed in ca entry
: VERSION OF PUMP + DECAY (decay can be viewed as simplified buffering)
: All variables are range variables
: This mechanism was published in:  Destexhe, A. Babloyantz, A. and 
: Sejnowski, TJ.  Ionic mechanisms for intrinsic slow oscillations in
: thalamic relay neurons. Biophys. J. 65: 1538-1552, 1993)
: Written by Alain Destexhe, Salk Institute, Nov 12, 1992


	USEION ca READ ica, cai WRITE cai
	GLOBAL depth,cainf,taur

	(molar) = (1/liter)			: moles do not appear in units
	(mM)	= (millimolar)
	(um)	= (micron)
	(mA)	= (milliamp)
	(msM)	= (ms mM)
	FARADAY = (faraday) (coulomb)

	depth	= .1	(um)		: depth of shell
	taur	= 50	(ms)		: rate of calcium removal
	cainf	= 100e-6(mM)
	cai		(mM)

	ca		(mM) <1e-5>

	ca = cainf
	cai = ca

	ica		(mA/cm2)
	drive_channel	(mM/ms)
	SOLVE state METHOD derivimplicit


	drive_channel =  - (10000) * ica / (2 * FARADAY * depth)
	if (drive_channel <= 0.) { drive_channel = 0. }	: cannot pump inward

	ca' = drive_channel + (cainf-ca)/taur
	cai = ca