» Articles » PMID: 26746357

Calcium Regulation of HCN Channels Supports Persistent Activity in a Multiscale Model of Neocortex

Overview
Journal Neuroscience
Specialty Neurology
Date 2016 Jan 10
PMID 26746357
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Neuronal persistent activity has been primarily assessed in terms of electrical mechanisms, without attention to the complex array of molecular events that also control cell excitability. We developed a multiscale neocortical model proceeding from the molecular to the network level to assess the contributions of calcium (Ca(2+)) regulation of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels in providing additional and complementary support of continuing activation in the network. The network contained 776 compartmental neurons arranged in the cortical layers, connected using synapses containing AMPA/NMDA/GABAA/GABAB receptors. Metabotropic glutamate receptors (mGluR) produced inositol triphosphate (IP3) which caused the release of Ca(2+) from endoplasmic reticulum (ER) stores, with reuptake by sarco/ER Ca(2+)-ATP-ase pumps (SERCA), and influence on HCN channels. Stimulus-induced depolarization led to Ca(2+) influx via NMDA and voltage-gated Ca(2+) channels (VGCCs). After a delay, mGluR activation led to ER Ca(2+) release via IP3 receptors. These factors increased HCN channel conductance and produced firing lasting for ∼1min. The model displayed inter-scale synergies among synaptic weights, excitation/inhibition balance, firing rates, membrane depolarization, Ca(2+) levels, regulation of HCN channels, and induction of persistent activity. The interaction between inhibition and Ca(2+) at the HCN channel nexus determined a limited range of inhibition strengths for which intracellular Ca(2+) could prepare population-specific persistent activity. Interactions between metabotropic and ionotropic inputs to the neuron demonstrated how multiple pathways could contribute in a complementary manner to persistent activity. Such redundancy and complementarity via multiple pathways is a critical feature of biological systems. Mediation of activation at different time scales, and through different pathways, would be expected to protect against disruption, in this case providing stability for persistent activity.

Citing Articles

Mechanism of an Intrinsic Oscillation in Rat Geniculate Interneurons.

Griffith E, Elsayed M, Dura-Bernal S, Neymotin S, Uhlrich D, Lytton W bioRxiv. 2024; .

PMID: 38895250 PMC: 11185623. DOI: 10.1101/2024.06.06.597830.


rdHSV-CA8 non-opioid analgesic gene therapy decreases somatosensory neuronal excitability by activating Kv7 voltage-gated potassium channels.

Kandel M, Zhuang G, Goins W, Marzulli M, Zhang M, Glorioso J Front Mol Neurosci. 2024; 17:1398839.

PMID: 38783904 PMC: 11112096. DOI: 10.3389/fnmol.2024.1398839.


Ultrafast simulation of large-scale neocortical microcircuitry with biophysically realistic neurons.

Olah V, Pedersen N, Rowan M Elife. 2022; 11.

PMID: 36341568 PMC: 9640191. DOI: 10.7554/eLife.79535.


Excitatory and inhibitory effects of HCN channel modulation on excitability of layer V pyramidal cells.

Maki-Marttunen T, Maki-Marttunen V PLoS Comput Biol. 2022; 18(9):e1010506.

PMID: 36099307 PMC: 9506642. DOI: 10.1371/journal.pcbi.1010506.


Insertion of Calcium-Permeable AMPA Receptors during Epileptiform Activity In Vitro Modulates Excitability of Principal Neurons in the Rat Entorhinal Cortex.

Amakhin D, Soboleva E, Chizhov A, Zaitsev A Int J Mol Sci. 2021; 22(22).

PMID: 34830051 PMC: 8621524. DOI: 10.3390/ijms222212174.


References
1.
Quian Quiroga R, Panzeri S . Extracting information from neuronal populations: information theory and decoding approaches. Nat Rev Neurosci. 2009; 10(3):173-85. DOI: 10.1038/nrn2578. View

2.
Compte A, Brunel N, Goldman-Rakic P, Wang X . Synaptic mechanisms and network dynamics underlying spatial working memory in a cortical network model. Cereb Cortex. 2000; 10(9):910-23. DOI: 10.1093/cercor/10.9.910. View

3.
De Young G, Keizer J . A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration. Proc Natl Acad Sci U S A. 1992; 89(20):9895-9. PMC: 50240. DOI: 10.1073/pnas.89.20.9895. View

4.
Neymotin S, Lee H, Fenton A, Lytton W . Interictal EEG discoordination in a rat seizure model. J Clin Neurophysiol. 2010; 27(6):438-44. DOI: 10.1097/WNP.0b013e3181fe059e. View

5.
Neymotin S, McDougal R, Sherif M, Fall C, Hines M, Lytton W . Neuronal calcium wave propagation varies with changes in endoplasmic reticulum parameters: a computer model. Neural Comput. 2015; 27(4):898-924. PMC: 4386758. DOI: 10.1162/NECO_a_00712. View