Relating Neuronal Firing Patterns to Functional Differentiation of Cerebral Cortex

Abstract

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. Neurons, or nerve cells in the brain, communicate with each other using stereotyped electric pulses, called spikes. It is believed that neurons convey information mainly through the frequency of the transmitted spikes, called the firing rate. In addition, neurons may communicate some information through the finer temporal patterns of the spikes. Neuronal firing patterns may depend on cellular organization, which varies among the regions of the brain, according to the roles they play, such as sensation, association, and motion. In order to examine the relationship among signals, structure, and function, we devised a metric to detect firing irregularity intrinsic and specific to individual neurons and analyzed spike sequences from over 1,000 neurons in 15 different cortical areas. Here we report two results of this study. First, we found that neurons exhibit stable firing patterns that can be characterized as “regular”, “random”, and “bursty”. Second, we observed a strong correlation between the type of signaling pattern exhibited by neurons in a given area and the function of that area. This suggests that, in addition to reflecting the cellular organization of the brain, neuronal signaling patterns may also play a role in specific types of neuronal computations.