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Calcini, N.

Publications and source records attributed to Calcini, N..

7 recordsLinked to original sources

Neuromodulatory Control of Cortical Function: Cell-Type Specific Regulation of Neuronal Information Transfer

Neuromodulatory systems such as dopamine and acetylcholine enable cortical circuits to rapidly shift between behavioral states, yet it remains unclear how receptor-specific signaling reshapes what single neurons compute. Here we combined whole-cell recordings from excitatory and inhibitory neurons in layer 2/3 of mouse somatosensory cortex with information-theoretic analyses under frozen-noise stimulation. We quantified stimulus-to-spike information transfer and profiled each neuron across four functional domains: passive membrane biophysics, action potential dynamics, intrinsic adaptation currents, and input feature selectivity captured by spike-triggered averages. Activation of D1, D2, or M1 receptors produced cell-type and receptor-specific changes in fractional information and firing output, demonstrating that neuromodulators regulate encoding beyond simple gain control. Unsupervised clustering revealed that receptor activation reshapes neuronal functional identities, consistent with a dynamic computational phenotype. To identify the organizing principle underlying these transitions, we applied multi-set correlation and factor analysis and found that neuromodulation systematically reorganizes covariance among functional domains. In excitatory neurons, dopaminergic activation led to a decreased coordination between input feature selectivity and other functional properties while strengthening coordination among response based features such as spike dynamics and adaptation. Inhibitory neurons, by contrast, generally exhibited increased coordination across domains. These findings identify neuromodulation as a reconfiguration signal that reshapes not only individual cellular properties but also the architecture linking them, thereby dynamically expanding the computational repertoire of cortical circuits.

neuroscience↗

Electrical diversity of neurons in sensory cortices

The classification of neuronal types is a complex task with numerous molecular, anatomical, and functional (electrical) features have been identified as informative in discriminating neuronal populations. The functional characterization of neurons has traditionally been carried out with predefined sets of parameters such as firing rate and action potential generation threshold. Here we provide an objective method to choose what parameters are most informative about a neurons functional cell type. Using this method we show that despite the significant molecular and anatomical variability across neurons, functional characterization of neuronal activity identifies 9 and 11 distinct neuronal subpopulations in the upper layers of the somatosensory and visual cortices respectively. This novel classification method will help to unravel the functional (electrophysiological) diversity of cellular classes throughout the nervous system. Further, the thorough comparison between the different classes of cells will provide a solid building block for the study of the sensory cortices.

neuroscience↗

Nonlinear super-resolution signal processing for subcellular analysis of calcium dynamics

Fluorescence imaging of calcium dynamics has revolutionized cellular biology, and especially neuroscience as it allows the study of neural activity across spatially well defined populations. Quantification of fluorescence signals is commonly performed using ratiometric measures. These measures, such as {Delta}F/F, are easy to implement, but they depend on the definition of a baseline, which is often not trivial outside of the measurement of evoked responses, and needs to be defined for every cell (or other cellular compartment) separately. Here, we present a new quantitative measure of fluorescence by taking advantage of the time dimension of the signal. The new method, which we named ARES (Autoregressive RESiduals), is based on the quantification of residuals after linear autoregression and does not require arbitrary baseline assignment. We detail the basic characteristics of the ARES signal, compare it against {Delta}F/F, and quantify the improvement in spatial and temporal resolution of recorded calcium data. We further exemplify its utility in the study of intracellular calcium dynamics by describing the propagation of a calcium wave inside a dendrite. As a robust and accurate method for quantifying fluorescence signals, ARES is particularly well-suited for the study of spontaneous as well as evoked calcium dynamics, subcellular localization of calcium signals, and spatiotemporal tracking of calcium dynamics. HighlightsO_LIA baseline-free quantitative measure of fluorescence is introduced C_LIO_LIThe method, called ARES, is based on autoregression C_LIO_LIARES improves the spatiotemporal resolution of calcium imaging recordings C_LIO_LIIts utility for the localization and spatiotemporal tracking of calcium is shown C_LI

neuroscience↗

A whole-cell recording database of neuromodulatory action in the adult neocortex

BackgroundThe recent release of two large intracellular electrophysiological databases now allows high-dimensional systematic analysis of mechanisms of information processing in the neocortex. Here, to complement these efforts, we introduce a freely and publicly available database that provides a comparative insight into the role of various neuromodulatory transmitters in controlling neural information processing. FindingsA database of in vitro whole-cell patch-clamp recordings from primary somatosensory and motor cortices (layers 2/3) of the adult mice (2-15 months old) from both sexes is introduced. A total of 464 current-clamp experiments from identified excitatory and inhibitory neurons are provided. Experiments include recordings with (i) Step-and-Hold protocol during which the current was transiently held at 10 steps, gradually increasing in amplitude, (ii) "Frozen Noise" injections that model the amplitude and time-varying nature of synaptic inputs to a neuron in biological networks. All experiments follow a within neuron across drug design which includes a vehicle control and a modulation of one of the following targets in the same neuron: dopamine and its receptors D1R, D2R, serotonin 5HT1f receptor, norepinephrine Alpha1, and acetylcholine M1 receptors. ConclusionsThis dataset is the first to provide a systematic and comparative insight into the role of the selected neuromodulators in controlling cellular excitability. The data will help to mechanistically address how bottom-up information processing can be modulated, providing a reference for studying neural coding characteristics and revealing the contribution of neuromodulation to information processing.

neuroscience↗

Cell type specific information transfer for sparse coding

Sensory neurons reconstruct the world from action potentials (spikes) impinging on them. To effectively transfer information about the stimulus to the next processing level, a neuron needs to be able to adapt its working range to the properties of the stimulus. Here, we focus on the intrinsic neural properties that influence information transfer in cortical neurons and how tightly their properties need to be tuned to the stimulus statistics for them to be effective. We start by measuring the intrinsic information encoding properties of putative excitatory and inhibitory neurons in L2/3 of the mouse barrel cortex. Excitatory neurons show high thresholds and strong adaptation, making them fire sparsely and resulting in a strong compression of information, whereas inhibitory neurons that favour fast spiking transfer more information. Next, we turn to computational modelling and ask how two properties influence information transfer: 1) spike-frequency adaptation and 2) the shape of the IV-curve. We find that a subthreshold (but not threshold) adaptation, the h-current, and a properly tuned leak conductance can increase the information transfer of a neuron, whereas threshold adaptation can increase its working range. Finally, we verify the effect of the IV-curve slope in our experimental recordings and show that excitatory neurons form a more heterogeneous population than inhibitory neurons. These relationships between intrinsic neural features and neural coding that had not been quantified before will aid computational, theoretical and systems neuroscientists in understanding how neuronal populations can alter their coding properties, such as through the impact of neuromodulators. Why the variability of intrinsic properties of excitatory neurons is larger than that of inhibitory ones is an exciting question, for which future research is needed. Author summaryIntracellular information transfer from synaptic input to output spike train is necessarily lossy. Here, we explicitly measure the mutual information between a neurons input and spike output and show that information transfer is more lossy and heterogeneous for excitatory than for inhibitory neurons. By using computational modelling we show that the shape of the input-output curve as well as how fast a neuron adapts to its input collectively determine the rate of information loss. These insights will help both experimentalists and modellers in designing and simulating experiments that investigate how network coding properties can adapt to the environment, for instance through the effects of neuromodulators.

neuroscience↗

Assessing the utility of MAGNETO to control neuronal excitability in the somatosensory cortex

Magnetic neuromodulation has outstanding promise for the development of novel neural interfaces without direct physical intervention with the brain. Here we tested the utility of Magneto in the adult somatosensory cortex by performing whole-cell intracellular recordings in vitro and extracellular recordings in freely moving mice. Results show that magnetic stimulation does not alter subthreshold membrane excitability or contribute to the generation of action potentials in virally transduced neurons expressing Magneto.

neuroscience↗

A databank for intracellular electrophysiological mapping of the adult somatosensory cortex

BackgroundNeurons in the supragranular layers of the somatosensory cortex integrate sensory (bottom-up) and cognitive/perceptual (top-down) information as they orchestrate communication across cortical columns. It has been inferred, based on intracellular recordings from juvenile animals, that supragranular neurons are electrically mature by the fourth postnatal week. However, the dynamics of the neuronal integration in the adulthood is largely unknown. Electrophysiological characterization of the active properties of these neurons throughout adulthood will help to address the biophysical and computational principles of the neuronal integration.\n\nFindingsHere we provide a database of whole-cell intracellular recordings from 315 neurons located in the supragranular layers (L2/3) of the primary somatosensory cortex in adult mice (9-45 weeks old) from both sexes (females, N=195; males, N=120). Data include 361 somatic current-clamp (CC) and 476 voltage-clamp (VC) experiments, recorded using a step-and-hold protocol (CC, N=257; VC, N=46), frozen noise injections (CC, N=104) and triangular voltage sweeps (VC, 10 (N=132), 50 (N=146) and 100 ms (N=152)), from regular spiking (N=169) and fast-spiking neurons (N=66).\n\nConclusionsThe data can be used to systematically study the properties of somatic integration, and the principles of action potential generation across sexes and across electrically characterized neuronal classes in adulthood. Understanding the principles of the somatic transformation of postsynaptic potentials into action potentials will shed light onto the computational principles of intracellular information transfer in single neurons and information processing in neuronal networks, helping to recreate neuronal functions in artificial systems.

neuroscience↗