» Articles » PMID: 25352777

Model Cerebellar Granule Cells Can Faithfully Transmit Modulated Firing Rate Signals

Overview
Specialty Cell Biology
Date 2014 Oct 30
PMID 25352777
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

A crucial assumption of many high-level system models of the cerebellum is that information in the granular layer is encoded in a linear manner. However, granule cells are known for their non-linear and resonant synaptic and intrinsic properties that could potentially impede linear signal transmission. In this modeling study we analyse how electrophysiological granule cell properties and spike sampling influence information coded by firing rate modulation, assuming no signal-related, i.e., uncorrelated inhibitory feedback (open-loop mode). A detailed one-compartment granule cell model was excited in simulation by either direct current or mossy-fiber synaptic inputs. Vestibular signals were represented as tonic inputs to the flocculus modulated at frequencies up to 20 Hz (approximate upper frequency limit of vestibular-ocular reflex, VOR). Model outputs were assessed using estimates of both the transfer function, and the fidelity of input-signal reconstruction measured as variance-accounted-for. The detailed granule cell model with realistic mossy-fiber synaptic inputs could transmit information faithfully and linearly in the frequency range of the vestibular-ocular reflex. This was achieved most simply if the model neurons had a firing rate at least twice the highest required frequency of modulation, but lower rates were also adequate provided a population of neurons was utilized, especially in combination with push-pull coding. The exact number of neurons required for faithful transmission depended on the precise values of firing rate and noise. The model neurons were also able to combine excitatory and inhibitory signals linearly, and could be replaced by a simpler (modified) integrate-and-fire neuron in the case of high tonic firing rates. These findings suggest that granule cells can in principle code modulated firing-rate inputs in a linear manner, and are thus consistent with the high-level adaptive-filter model of the cerebellar microcircuit.

Citing Articles

Excitatory synaptic integration mechanism of three types of granule cells in the dentate gyrus.

Mao Y, Liu M, Sun X Cogn Neurodyn. 2025; 19(1):40.

PMID: 39944109 PMC: 11811379. DOI: 10.1007/s11571-025-10226-0.


Cerebellar-driven cortical dynamics can enable task acquisition, switching and consolidation.

Pemberton J, Chadderton P, Costa R Nat Commun. 2024; 15(1):10913.

PMID: 39738061 PMC: 11686095. DOI: 10.1038/s41467-024-55315-6.


Mechanisms Underlying Mu Opioid Receptor Effects on Parallel Fiber-Purkinje Cell Synaptic Transmission in Mouse Cerebellar Cortex.

Yang Y, Bai J, Sun J, Ye T, Zhang L, Wu F Front Synaptic Neurosci. 2022; 14:862704.

PMID: 35546898 PMC: 9083459. DOI: 10.3389/fnsyn.2022.862704.


Culturing and patch clamping of Jurkat T cells and neurons on AlO coated nanowire arrays of altered morphology.

Harberts J, Zierold R, Fendler C, Koitmae A, Bayat P, Fernandez-Cuesta I RSC Adv. 2022; 9(20):11194-11201.

PMID: 35520244 PMC: 9063011. DOI: 10.1039/c8ra05320k.


Optimization of Efficient Neuron Models With Realistic Firing Dynamics. The Case of the Cerebellar Granule Cell.

Marin M, Saez-Lara M, Ros E, Garrido J Front Cell Neurosci. 2020; 14:161.

PMID: 32765220 PMC: 7381211. DOI: 10.3389/fncel.2020.00161.


References
1.
DAngelo E, De Zeeuw C . Timing and plasticity in the cerebellum: focus on the granular layer. Trends Neurosci. 2008; 32(1):30-40. DOI: 10.1016/j.tins.2008.09.007. View

2.
Gerstner W . Population dynamics of spiking neurons: fast transients, asynchronous states, and locking. Neural Comput. 2000; 12(1):43-89. DOI: 10.1162/089976600300015899. View

3.
Brunel N, Chance F, Fourcaud N, Abbott L . Effects of synaptic noise and filtering on the frequency response of spiking neurons. Phys Rev Lett. 2001; 86(10):2186-9. DOI: 10.1103/PhysRevLett.86.2186. View

4.
Tabak S, COLLEWIJN H, Boumans L, van der Steen J . Gain and delay of human vestibulo-ocular reflexes to oscillation and steps of the head by a reactive torque helmet. I. Normal subjects. Acta Otolaryngol. 1998; 117(6):785-95. DOI: 10.3109/00016489709114203. View

5.
DAngelo E, Nieus T, Maffei A, Armano S, Rossi P, Taglietti V . Theta-frequency bursting and resonance in cerebellar granule cells: experimental evidence and modeling of a slow k+-dependent mechanism. J Neurosci. 2001; 21(3):759-70. PMC: 6762330. View