Conversions between space and time in network dynamics by neural assemblies
The connectivity structure of many biological systems, including neural circuits, is highly non-uniform. Recent technologies allow detailed mapping of these irregularities, but our understanding of their effect on the overall circuit dynamics is still lacking. By developing complex system analytical tools that perform reduction of the network, I determine the impact of connectivity features on network dynamics. I will demonstrate the use of these tools on neural assemblies (clusters), a ubiquitous non-uniform structure in our brains. I will show how neural assemblies of different sizes naturally generate multiple timescales of activity spanning several orders of magnitude. I will demonstrate how the analytical theory we develop for rate networks, supported by spiking network simulations, reveals the dependency between neural timescales and assembly sizes and how new recordings of spontaneous activity from a million neurons support this analysis. I will also show how our model can naturally explain the particular long-tailed timescale distribution observed in the awake primate cortex. In olfactory cortex, neural assemblies represent odor stimuli. Previously, I showed how the diffuse recurrent excitation among these assemblies allows the conversion of time-encoded inputs from the bulb to spacial neural assembly representations in olfactory cortex. Here, I will show how changes in the dynamical properties of these assemblies alter both their timing response and properties of the time-encoded inputs via feedback. This demonstrates the role of neural assemblies in time-sensitive modulation needed for cognitive tasks, such as attention. Our results offer a biologically plausible mechanism of assemblies in network connectivity for explaining multiple puzzling dynamical phenomena: The ability of neural circuits to transform external simultaneous temporal fluctuations into spatial representations and alter them; and the ability of neuronal circuits to generate simultaneous temporal fluctuations across a large range of timescales; Presented in the van Vreeswijk Theoretical Neuroscience Seminar series (formerly WWTNS) on 2024-03-20. Recording duration: 00:41:28.
Experience dependent changes of sensory representation in the olfactory cortex
Sensory representations are typically thought as neuronal activity patterns that encode physical attributes of the outside world. However, increasing evidence is showing that as animals learned the association between a sensory stimulus and its behavioral relevance, stimulus representation in sensory cortical areas can change. In this seminar I will present recent experiments from our lab showing that the activity in the olfactory piriform cortex (PC) of mice encodes not only odor information, but also non-olfactory variables associated with the behavioral task. By developing an associative olfactory learning task, in which animals learn to associate a particular context with an odor and a reward, we were able to record the activity of multiple neurons as the animal runs in a virtual reality corridor. By analyzing the population activity dynamics using Principal Components Analysis, we find different population trajectories evolving through time that can discriminate aspects of different trial types. By using Generalized Linear Models we further dissected the contribution of different sensory and non-sensory variables to the modulation of PC activity. Interestingly, the experiments show that variables related to both sensory and non-sensory aspects of the task (e.g., odor, context, reward, licking, sniffing rate and running speed) differently modulate PC activity, suggesting that the PC adapt odor processing depending on experience and behavior.
Circuit and synaptic mechanisms of plasticity in neural ensembles
Inhibitory microcircuits play an important role regulating cortical responses to sensory stimuli. Interneurons that inhibit dendritic or somatic integration are gatekeepers for neural activity, synaptic plasticity and the formation of sensory representations. We have been investigating the synaptic plasticity mechanisms underlying the formation of ensembles in olfactory and orbitofrontal cortex. We have been focusing on the roles of three inhibitory neuron classes in gating excitatory synaptic plasticity in olfactory cortex- somatostatin (SST-INs), parvalbumin (PV-INs), and vasoactive intestinal polypeptide (VIP-INs) interneurons. Further, we are investigating the rules for inhibitory plasticity and a potential role in stabilizing ensembles in associative cortices. I will present new findings to support distinct roles for different interneuron classes in the gating and stabilization of ensemble representations of olfactory responses.