» Articles » PMID: 36408073

Disynaptic Effect of Hilar Cells on Pattern Separation in a Spiking Neural Network of Hippocampal Dentate Gyrus

Overview
Journal Cogn Neurodyn
Publisher Springer
Specialty Neurology
Date 2022 Nov 21
PMID 36408073
Authors
Affiliations
Soon will be listed here.
Abstract

We study the disynaptic effect of the hilar cells on pattern separation in a spiking neural network of the hippocampal dentate gyrus (DG). The principal granule cells (GCs) in the DG perform pattern separation, transforming similar input patterns into less-similar output patterns. In our DG network, the hilus consists of excitatory mossy cells (MCs) and inhibitory HIPP (hilar perforant path-associated) cells. Here, we consider the disynaptic effects of the MCs and the HIPP cells on the GCs, mediated by the inhibitory basket cells (BCs) in the granular layer; MC BC GC and HIPP BC GC. The MCs provide disynaptic inhibitory input (mediated by the intermediate BCs) to the GCs, which decreases the firing activity of the GCs. On the other hand, the HIPP cells disinhibit the intermediate BCs, which leads to increasing the firing activity of the GCs. In this way, the disynaptic effects of the MCs and the HIPP cells are opposite. We investigate change in the pattern separation efficacy by varying the synaptic strength [from the pre-synaptic X (= MC or HIPP) to the post-synaptic BC]. Thus, sparsity for the firing activity of the GCs is found to improve the efficacy of pattern separation, and hence the disynaptic effects of the MCs and the HIPP cells on the pattern separation become opposite ones. In the combined case when simultaneously changing both and , as a result of balance between the two competing disynaptic effects of the MCs and the HIPP cells, the efficacy of pattern separation is found to become the highest at their original default values where the activation degree of the GCs is the lowest. We also note that, while the GCs perform pattern separation, sparsely synchronized rhythm is found to appear in the population of the GCs. Hence, we examine quantitative association between population and individual firing behaviors in the sparsely synchronized rhythm and pattern separation. They are found to be strongly correlated. Consequently, the better the population and individual firing behaviors in the sparsely synchronized rhythm are, the more pattern separation efficacy becomes enhanced.

Citing Articles

Regulation of dentate gyrus pattern separation by hilus ectopic granule cells.

Yin H, Sun X, Yang K, Lan Y, Lu Z Cogn Neurodyn. 2025; 19(1):10.

PMID: 39801911 PMC: 11718051. DOI: 10.1007/s11571-024-10204-y.


Effect of adult hippocampal neurogenesis on pattern separation and its applications.

Wang Z, Yang K, Sun X Cogn Neurodyn. 2024; 18(5):1-14.

PMID: 39568526 PMC: 11564429. DOI: 10.1007/s11571-024-10110-3.


Quantifying harmony between direct and indirect pathways in the basal ganglia: healthy and Parkinsonian states.

Kim S, Lim W Cogn Neurodyn. 2024; 18(5):2809-2829.

PMID: 39555274 PMC: 11564607. DOI: 10.1007/s11571-024-10119-8.


Adult neurogenesis in the hippocampal dentate gyrus affects sparsely synchronized rhythms, associated with pattern separation and integration.

Kim S, Lim W Cogn Neurodyn. 2024; 18(5):2311-2321.

PMID: 39555267 PMC: 11564722. DOI: 10.1007/s11571-024-10089-x.


Effect of adult-born immature granule cells on pattern separation in the hippocampal dentate gyrus.

Kim S, Lim W Cogn Neurodyn. 2024; 18(4):2077-2093.

PMID: 39104672 PMC: 11297892. DOI: 10.1007/s11571-023-09985-5.

References
1.
de Almeida L, Idiart M, Lisman J . A second function of gamma frequency oscillations: an E%-max winner-take-all mechanism selects which cells fire. J Neurosci. 2009; 29(23):7497-503. PMC: 2758634. DOI: 10.1523/JNEUROSCI.6044-08.2009. View

2.
Myers C, Bermudez-Hernandez K, Scharfman H . The influence of ectopic migration of granule cells into the hilus on dentate gyrus-CA3 function. PLoS One. 2013; 8(6):e68208. PMC: 3695928. DOI: 10.1371/journal.pone.0068208. View

3.
Scharfman H, Myers C . Hilar mossy cells of the dentate gyrus: a historical perspective. Front Neural Circuits. 2013; 6:106. PMC: 3572871. DOI: 10.3389/fncir.2012.00106. View

4.
Kneisler T, Dingledine R . Spontaneous and synaptic input from granule cells and the perforant path to dentate basket cells in the rat hippocampus. Hippocampus. 1995; 5(3):151-64. DOI: 10.1002/hipo.450050302. View

5.
Beck H, Goussakov I, Lie A, Helmstaedter C, Elger C . Synaptic plasticity in the human dentate gyrus. J Neurosci. 2000; 20(18):7080-6. PMC: 6772802. View