Topic: inhibitory neurons

Cellular crosstalk is an essential process during brain development and is influenced by numerous factors, including cell morphology, adhesion, the local extracellular matrix and secreted vesicles. Inspired by mutations associated with neurodevelopmental disorders, we focus on understanding the role of extracellular mechanisms essential for the proper development of the human brain. Therefore, we combine 2D and 3D in vitro human models to better understand the molecular and cellular mechanisms involved in progenitor proliferation and fate, migration and maturation of excitatory and inhibitory

Classical views suggest that memories are stored in assemblies of excitatory neurons that become strongly interconnected during learning. However, recent experimental and theoretical results have challenged this view, leading to the hypothesis that memories are encoded in assemblies containing both excitatory (E) and inhibitory (I) neurons. Understanding the effects of these E-I assemblies on memory function is therefore essential. Using a biologically constrained model of an olfactory memory network, I will first describe how introducing E-I assemblies reorganizes odor-evoked activity pattern

Cellular crosstalk is an essential process during brain development and it is influenced by numerous factors, including the morphology of the cells, their adhesion molecules, the local extracellular matrix and the secreted vesicles. Inspired by mutations associated with neurodevelopmental disorders, we focus on understanding the role of extracellular mechanisms essential for the correct development of the human brain. Hence, we combine the in vivo mouse model and the in vitro human-derived neurons, cerebral organoids, and dorso-ventral assembloids in order to better comprehend the molecular an

In this study, we aim to broaden our understanding of the mouse’s primary visual cortex by modeling data provided by the datasets from Stringer et al. (2019) and the Allen Institute. We investigated the roles of the different excitatory and inhibitory cell types in the visual cortex whose functions remain unclear. Using the Stringer dataset, we explored the correlation between the activity of excitatory cells in the mouse visual cortex and mouse running behavior without any visual input. Principle Component Analysis (PCA) was applied to reduce the dimension of our neuron activity data of 119

Transcriptomics has revealed that cortical inhibitory neurons exhibit a great diversity of fine molecular subtypes, but it is not known whether these subtypes have correspondingly diverse activity patterns in the living brain. We show that inhibitory subtypes in primary visual cortex (V1) have diverse correlates with brain state, but that this diversity is organized by a single factor: position along their main axis of transcriptomic variation. We combined in vivo 2-photon calcium imaging of mouse V1 with a novel transcriptomic method to identify mRNAs for 72 selected genes in ex vivo slices.

Modeling brain mechanisms is often confined to a given scale, such as single-cell models, network models or whole-brain models, and it is often difficult to relate these models. Here, we show an approach to build models across scales, starting from the level of circuits to the whole brain. The key is the design of accurate population models derived from biophysical models of networks of excitatory and inhibitory neurons, using mean-field techniques. Such population models can be later integrated as units in large-scale networks defining entire brain areas or the whole brain. We illustrate this

Episodic memories are encoded by sparse populations of neurons activated during an experience. These neural ensembles constitute memory engrams that are both necessary and sufficient for inducing recall even long after memory acquisition. This suggests that following encoding, engrams are stabilized to support reliable memory retrieval. However, little is known about the temporal evolution of engrams over the course of memory consolidation or how it impacts mnemonic properties. Here we employed computational and experimental approaches to examine how the composition and selectivity of engrams

Optogenetics is a powerful tool that allows experimentalists to perturb neural circuits. What can we learn about a network from observing its response to perturbations? I will first describe the results of optogenetic activation of inhibitory neurons in mice cortex, and show that the results are consistent with inhibition stabilization. I will then move to experiments in which excitatory neurons are activated optogenetically, with or without visual inputs, in mice and monkeys. In some conditions, these experiments show a surprising result that the distribution of firing rates is not significan

We use the olfactory system and forebrain of (adult) zebrafish as a model to analyze how relevant information is extracted from sensory inputs, how information is stored in memory circuits, and how sensory inputs inform behavior. A series of recent findings provides evidence that inhibition has not only homeostatic functions in neuronal circuits but makes highly specific, instructive contributions to behaviorally relevant computations in different brain regions. These observations imply that the connectivity among excitatory and inhibitory neurons exhibits essential higher-order structure that

Inhibitory neurons take on many forms and functions. How this diversity contributes to memory function is not completely known. Previous formal studies indicate inhibition differentiated by local and global connectivity in associative memory networks functions to rescale the level of retrieval of excitatory assemblies. However, such studies lack biological details such as a distinction between types of neurons (excitatory and inhibitory), unrealistic connection schemas, and non-sparse assemblies. In this study, we present a rate-based cortical model where neurons are distinguished (as excitato

Motivational drives are internal states that can be different even in similar interactions with external stimuli. Curiosity as the motivational drive for novelty-seeking and investigating the surrounding environment is for survival as essential and intrinsic as hunger. Curiosity, hunger, and appetitive aggression drive three different goal-directed behaviors—novelty seeking, food eating, and hunting— but these behaviors are composed of similar actions in animals. This similarity of actions has made it challenging to study novelty seeking and distinguish it from eating and hunting in nonarticul

The vIRt nucleus in the medulla, composed of mainly inhibitory neurons, is necessary for whisking rhythm generation. It innervates motoneurons in the facial nucleus (FN) that project to intrinsic vibrissa muscles. The nearby pre-Bötzinger complex (pBötC), which generates inhalation, sends inhibitory inputs to the vIRt nucleus which contribute to the synchronization of vIRt neurons. Lower-amplitude periodic whisking, however, can occur after decay of the pBötC signal. To explain how vIRt network generates these “intervening” whisks by bursting in synchrony, and how pBötC input induces strong w

Activity-dependent structural plasticity (ADSP) plays a significant role in the homeostatic regulation of neuronal connectivity and activity in developing neuronal networks. This process involves intricate activity-dependent interaction between neuronal growth and migration, which shapes synaptic connections and results in network architectures with varying levels of clustering and modularity, influenced by the initial conditions. While excitatory interactions are essential for early network formation, the timely maturation of inhibition is also considered essential for stable activity dynamic

Inhibitory neurons (I), akin to their excitatory (E) counterparts, adjust synaptic efficacies in response to neural activity. Contrary to the traditional view of inhibition as a purely global activity modulator, recent studies highlighted the importance of specificity in (E/I) wiring and motif structures. These motifs, encompassing mutual and lateral inhibition, take essential functional roles in tuning of receptive fields, learning of representations, predictive coding, and in the regulation of the degrees of freedom of the network’s dynamics (i.e. the network dimensionality). Despite numero

Coherent oscillations of neural activity are ubiquitous across brain spatial and temporal scales and have been associated with the formation of sensory or behavioral representations [1]. Refined experimental techniques report today a new complexity of this oscillatory activity, especially in the gamma (30-100 Hz) band. Indeed, the frequency of these oscillations shows a large variability through time [2], questioning the classical view of γ oscillations being separated into different frequency bands. Oscillations appear instead in bursts characterised by rapid, synchronous neuronal firing. Thi

The hippocampus plays a central role in memory processing. In order to avoid deleterious interference between stored and ongoing experience, theoretical considerations require a separation between phases of memory encoding and recall within the same neural circuit, putatively controlled by hippocampal theta oscillations [1]. However, the neural mechanisms subserving this separation remain unknown. Classical models either remain moot about these mechanisms [2], or assume purpose-built neuromodulatory interactions that are in conflict with biologically realistic timescales of synaptic modulation

Network models of cortex typically focus on excitatory population dynamics, relegating inhibition to a support role. However, recent studies have shown that memories can be encoded by both excitatory and inhibitory neurons (EI engrams), adding to the evidence of the functional importance of inhibitory neurons beyond mere stabilization. The functional consequence of such EI engrams is unclear, and the synaptic plasticity rules that could sustain them are unknown. Here, we explore in silico a mechanism for EI engrams storage and recall to glean possible computational benefits of such engrams ove