Estimating nonstationary inputs from a single spike train based on a neuron model with adaptation.

Because every spike of a neuron is determined by input signals, a train of spikes may contain information about the dynamics of unobserved neurons. A state-space method based on the leaky integrate-and-fire model, describing neuronal transformation from input signals to a spike train has been proposed for tracking input parameters represented by their mean and fluctuation [11]. In the present paper, we propose to make the estimation more realistic by adopting an LIF model augmented with an adaptive moving threshold. Moreover, because the direct state-space method is computationally infeasible for a data set comprising thousands of spikes, we further develop a practical method for transforming instantaneous firing characteristics back to input parameters. The instantaneous firing characteristics, represented by the firing rate and non-Poisson irregularity, can be estimated using a computationally feasible algorithm. We applied our proposed methods to synthetic data to clarify that they perform well.

Estimating inputs and an internal neuronal parameter from a single spike train.

Because neurons are integrating input signals and translating them into timed output spikes, examining spike timing may reveal information about inputs, such as population activities of excitatory and inhibitory presynaptic neurons. Here we construct a state-space method for estimating not only such extrinsic parameters, but also an intrinsic neuronal parameter such as the membrane time constant from a single spike train.

Estimating nonstationary input signals from a single neuronal spike train.

Neurons temporally integrate input signals, translating them into timed output spikes. Because neurons nonperiodically emit spikes, examining spike timing can reveal information about input signals, which are determined by activities in the populations of excitatory and inhibitory presynaptic neurons. Although a number of mathematical methods have been developed to estimate such input parameters as the mean and fluctuation of the input current, these techniques are based on the unrealistic assumption that presynaptic activity is constant over time. Here, we propose tracking temporal variations in input parameters with a two-step analysis method. First, nonstationary firing characteristics comprising the firing rate and non-Poisson irregularity are estimated from a spike train using a computationally feasible state-space algorithm. Then, information about the firing characteristics is converted into likely input parameters over time using a transformation formula, which was constructed by inverting the neuronal forward transformation of the input current to output spikes. By analyzing spike trains recorded in vivo, we found that neuronal input parameters are similar in the primary visual cortex V1 and middle temporal area, whereas parameters in the lateral geniculate nucleus of the thalamus were markedly different.

Neurons as ideal change-point detectors.

Every computational unit in the brain monitors incoming signals, instant by instant, for meaningful changes in the face of stochastic fluctuation. Recent studies have suggested that even a single neuron can detect changes in noisy signals. In this paper, we demonstrate that a single leaky integrate-and-fire neuron can achieve change-point detection close to that of theoretical optimal, for uniform-rate process, functions even better than a Bayes-optimal algorithm when the underlying rate deviates from a presumed uniform rate process. Given a reasonable number of synaptic connections (order 10(4)) and the rate of the input spike train, the values of the membrane time constant and the threshold found for optimizing change-point detection are close to those seen in biological neurons. These findings imply that biological neurons could act as sophisticated change-point detectors.

Elemental spiking neuron model for reproducing diverse firing patterns and predicting precise firing times.

In simulating realistic neuronal circuitry composed of diverse types of neurons, we need an elemental spiking neuron model that is capable of not only quantitatively reproducing spike times of biological neurons given in vivo-like fluctuating inputs, but also qualitatively representing a variety of firing responses to transient current inputs. Simplistic models based on leaky integrate-and-fire mechanisms have demonstrated the ability to adapt to biological neurons. In particular, the multi-timescale adaptive threshold (MAT) model reproduces and predicts precise spike times of regular-spiking, intrinsic-bursting, and fast-spiking neurons, under any fluctuating current; however, this model is incapable of reproducing such specific firing responses as inhibitory rebound spiking and resonate spiking. In this paper, we augment the MAT model by adding a voltage dependency term to the adaptive threshold so that the model can exhibit the full variety of firing responses to various transient current pulses while maintaining the high adaptability inherent in the original MAT model. Furthermore, with this addition, our model is actually able to better predict spike times. Despite the augmentation, the model has only four free parameters and is implementable in an efficient algorithm for large-scale simulation due to its linearity, serving as an element neuron model in the simulation of realistic neuronal circuitry.

Relating neuronal firing patterns to functional differentiation of cerebral cortex.

It has been empirically established that the cerebral cortical areas defined by Brodmann one hundred years ago solely on the basis of cellular organization are closely correlated to their function, such as sensation, association, and motion. Cytoarchitectonically distinct cortical areas have different densities and types of neurons. Thus, signaling patterns may also vary among cytoarchitectonically unique cortical areas. To examine how neuronal signaling patterns are related to innate cortical functions, we detected intrinsic features of cortical firing by devising a metric that efficiently isolates non-Poisson irregular characteristics, independent of spike rate fluctuations that are caused extrinsically by ever-changing behavioral conditions. Using the new metric, we analyzed spike trains from over 1,000 neurons in 15 cortical areas sampled by eight independent neurophysiological laboratories. Analysis of firing-pattern dissimilarities across cortical areas revealed a gradient of firing regularity that corresponded closely to the functional category of the cortical area; neuronal spiking patterns are regular in motor areas, random in the visual areas, and bursty in the prefrontal area. Thus, signaling patterns may play an important role in function-specific cerebral cortical computation.