» Articles » PMID: 37656758

A Multi-layer Mean-field Model of the Cerebellum Embedding Microstructure and Population-specific Dynamics

Overview
Specialty Biology
Date 2023 Sep 1
PMID 37656758
Authors
Affiliations
Soon will be listed here.
Abstract

Mean-field (MF) models are computational formalism used to summarize in a few statistical parameters the salient biophysical properties of an inter-wired neuronal network. Their formalism normally incorporates different types of neurons and synapses along with their topological organization. MFs are crucial to efficiently implement the computational modules of large-scale models of brain function, maintaining the specificity of local cortical microcircuits. While MFs have been generated for the isocortex, they are still missing for other parts of the brain. Here we have designed and simulated a multi-layer MF of the cerebellar microcircuit (including Granule Cells, Golgi Cells, Molecular Layer Interneurons, and Purkinje Cells) and validated it against experimental data and the corresponding spiking neural network (SNN) microcircuit model. The cerebellar MF was built using a system of equations, where properties of neuronal populations and topological parameters are embedded in inter-dependent transfer functions. The model time constant was optimised using local field potentials recorded experimentally from acute mouse cerebellar slices as a template. The MF reproduced the average dynamics of different neuronal populations in response to various input patterns and predicted the modulation of the Purkinje Cells firing depending on cortical plasticity, which drives learning in associative tasks, and the level of feedforward inhibition. The cerebellar MF provides a computationally efficient tool for future investigations of the causal relationship between microscopic neuronal properties and ensemble brain activity in virtual brain models addressing both physiological and pathological conditions.

Citing Articles

Model-agnostic neural mean field with a data-driven transfer function.

Spaeth A, Haussler D, Teodorescu M Neuromorphic Comput Eng. 2024; 4(3):034013.

PMID: 39310743 PMC: 11413991. DOI: 10.1088/2634-4386/ad787f.


Multiscale modeling of neuronal dynamics in hippocampus CA1.

Tesler F, Lorenzi R, Ponzi A, Casellato C, Palesi F, Gandolfi D Front Comput Neurosci. 2024; 18:1432593.

PMID: 39165754 PMC: 11333306. DOI: 10.3389/fncom.2024.1432593.


Model-Agnostic Neural Mean Field With The Refractory SoftPlus Transfer Function.

Spaeth A, Haussler D, Teodorescu M bioRxiv. 2024; .

PMID: 38370695 PMC: 10871173. DOI: 10.1101/2024.02.05.579047.

References
1.
Gagliano G, Monteverdi A, Casali S, Laforenza U, Wheeler-Kingshott C, DAngelo E . Non-Linear Frequency Dependence of Neurovascular Coupling in the Cerebellar Cortex Implies Vasodilation-Vasoconstriction Competition. Cells. 2022; 11(6). PMC: 8947624. DOI: 10.3390/cells11061047. View

2.
Savini G, Pardini M, Castellazzi G, Lascialfari A, Chard D, DAngelo E . Default Mode Network Structural Integrity and Cerebellar Connectivity Predict Information Processing Speed Deficit in Multiple Sclerosis. Front Cell Neurosci. 2019; 13:21. PMC: 6396736. DOI: 10.3389/fncel.2019.00021. View

3.
Glomb K, Ponce-Alvarez A, Gilson M, Ritter P, Deco G . Resting state networks in empirical and simulated dynamic functional connectivity. Neuroimage. 2017; 159:388-402. DOI: 10.1016/j.neuroimage.2017.07.065. View

4.
Auksztulewicz R, Friston K . Attentional Enhancement of Auditory Mismatch Responses: a DCM/MEG Study. Cereb Cortex. 2015; 25(11):4273-83. PMC: 4816780. DOI: 10.1093/cercor/bhu323. View

5.
Masoli S, Ottaviani A, Casali S, DAngelo E . Cerebellar Golgi cell models predict dendritic processing and mechanisms of synaptic plasticity. PLoS Comput Biol. 2020; 16(12):e1007937. PMC: 7837495. DOI: 10.1371/journal.pcbi.1007937. View