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A powerful experimental approach for investigating computation in networks of biological neurons is the use of cultured dissociated cortical cells grown into networks on a multi-electrode array. Such preparations allow investigation of network development, activity, plasticity, responses to stimuli, and the effects of pharmacological agents. They also exhibit whole-culture pathological bursting; understanding the mechanisms that underlie this could allow creation of more useful cell cultures and possibly have medical applications.
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Neurostimulation using weak electric fields has generated excitement in recent years due to its potential as a medical intervention. However, study of this stimulation modality has been hampered by inconsistent results and large variability within and between studies. In order to begin addressing this variability we need to properly characterise the impact of the current on the underlying neuron populations. To develop and test a computational model capable of capturing the impact of electric field stimulation on networks of neurons. We construct a cortical tissue model with distinct layers and explicit neuron morphologies. We then apply a model of electrical stimulation and carry out multiple test case simulations. The cortical slice model is compared to experimental literature and shown to capture the main features of the electrophysiological response to stimulation. Namely, the model showed 1) a similar level of depolarisation in individual pyramidal neurons, 2) acceleration of intrinsic oscillations, and 3) retention of the spatial profile of oscillations in different layers. We then apply alternative electric fields to demonstrate how the model can capture differences in neuronal responses to the electric field. We demonstrate that the tissue response is dependent on layer depth, the angle of the apical dendrite relative to the field, and stimulation strength. We present publicly available computational modelling software that predicts the neuron network population response to electric field stimulation.
Recently Segev et al. (Phys. Rev. E 64,2001, Phys.Rev.Let. 88, 2002) made long-term observations of spontaneous activity of in-vitro cortical networks, which differ from predictions of current models in many features. In this paper we generalize the EI cortical model introduced in a previous paper (S.Scarpetta et al. Neural Comput. 14, 2002), including intrinsic white noise and analyzing effects of noise on the spontaneous activity of the nonlinear system, in order to account for the experimental results of Segev et al.. Analytically we can distinguish different regimes of activity, depending from the model parameters. Using analytical results as a guide line, we perform simulations of the nonlinear stochastic model in two different regimes, B and C. The Power Spectrum Density (PSD) of the activity and the Inter-Event-Interval (IEI) distributions are computed, and compared with experimental results. In regime B the network shows stochastic resonance phenomena and noise induces aperiodic collective synchronous oscillations that mimic experimental observations at 0.5 mM Ca concentration. In regime C the model shows spontaneous synchronous periodic activity that mimic activity observed at 1 mM Ca concentration and the PSD shows two peaks at the 1st and 2nd harmonics in agreement with experiments at 1 mM Ca. Moreover (due to intrinsic noise and nonlinear activation function effects) the PSD shows a broad band peak at low frequency. This feature, observed experimentally, does not find explanation in the previous models. Besides we identify parametric changes (namely increase of noise or decreasing of excitatory connections) that reproduces the fading of periodicity found experimentally at long times, and we identify a way to discriminate between those two possible effects measuring experimentally the low frequency PSD.
During morphogenesis, the shape of a tissue emerges from collective cellular behaviors, which are in part regulated by mechanical and biochemical interactions between cells. Quantification of force and stress is therefore necessary to analyze the mechanisms controlling tissue morphogenesis. Recently, a mechanical measurement method based on force inference from cell shapes and connectivity has been developed. It is non-invasive, and can provide space-time maps of force and stress within an epithelial tissue, up to prefactors. We previously performed a comparative study of three force-inference methods, which differ in their approach of treating indefiniteness in an inverse problem between cell shapes and forces. In the present study, to further validate and compare the three force inference methods, we tested their robustness by measuring temporal fluctuation of estimated forces. Quantitative data of cell-level dynamics in a developing tissue suggests that variation of forces and stress will remain small within a short period of time ($sim$minutes). Here, we showed that cell-junction tensions and global stress inferred by the Bayesian force inference method varied less with time than those inferred by the method that estimates only tension. In contrast, the amplitude of temporal fluctuations of estimated cell pressures differs less between different methods. Altogether, the present study strengthens the validity and robustness of the Bayesian force-inference method.
For the nervous system to work at all, a delicate balance of excitation and inhibition must be achieved. However, when such a balance is sought by global strategies, only few modes remain balanced close to instability, and all other modes are strongly stable. Here we present a simple model of neural tissue in which this balance is sought locally by neurons following `anti-Hebbian behavior: {sl all} degrees of freedom achieve a close balance of excitation and inhibition and become critical in the dynamical sense. At long timescales, the modes of our model oscillate around the instability line, so an extremely complex breakout dynamics ensues in which different modes of the system oscillate between prominence and extinction. We show the system develops various anomalous statistical behaviours and hence becomes self-organized critical in the statistical sense.
During wakefulness and deep sleep brain states, cortical neural networks show a different behavior, with the second characterized by transients of high network activity. To investigate their impact on neuronal behavior, we apply a pairwise Ising model analysis by inferring the maximum entropy model that reproduces single and pairwise moments of the neurons spiking activity. In this work we first review the inference algorithm introduced in Ferrari,Phys. Rev. E (2016). We then succeed in applying the algorithm to infer the model from a large ensemble of neurons recorded by multi-electrode array in human temporal cortex. We compare the Ising model performance in capturing the statistical properties of the network activity during wakefulness and deep sleep. For the latter, the pairwise model misses relevant transients of high network activity, suggesting that additional constraints are necessary to accurately model the data.
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