ArticleJournal of neurophysiology2014
Cellular mechanisms for response heterogeneity among L2/3 pyramidal cells in whisker somatosensory cortex.
Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 21 citations in OpenAlex.
- A computational model elucidating mechanisms and variability in theta burst stimulation responses.Journal of computational neuroscience · 2024Article
- A latent pool of neurons silenced by sensory-evoked inhibition can be recruited to enhance perception.Neuron · 2024Article
- Transient enhancement of stimulus-evoked activity in neocortex during sensory learning.Learning & memory (Cold Spring Harbor, N.Y.) · 2024Article
- Diverse tuning underlies sparse activity in layer 2/3 vibrissal cortex of awake mice.The Journal of physiology · 2019Article
- Increased Excitation-Inhibition Ratio Stabilizes Synapse and Circuit Excitability in Four Autism Mouse Models.Neuron · 2019Article
- Organization of orientation-specific whisker deflection responses in layer 2/3 of mouse somatosensory cortex.Neuroscience · 2018Article
- Article
- High-velocity stimulation evokes "dense" population response in layer 2/3 vibrissal cortex.Journal of neurophysiology · 2017Article
- Inhibitory Circuits in Cortical Layer 5.Frontiers in neural circuits · 2016Review
- Article
- Decoding thalamic afferent input using microcircuit spiking activity.Journal of neurophysiology · 2015Article
- Structure of a single whisker representation in layer 2 of mouse somatosensory cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
Abstract
Whisker deflection evokes sparse, low-probability spiking among L2/3 pyramidal cells in rodent somatosensory cortex (S1), with spiking distributed nonuniformly between more and less responsive cells. The cellular and local circuit factors that determine whisker responsiveness across neurons are unclear. To identify these factors, we used two-photon calcium imaging and loose-seal recording to identify more and less responsive L2/3 neurons in S1 slices in vitro, during feedforward recruitment of the L2/3 network by L4 stimulation. We observed a broad gradient of spike recruitment thresholds within local L2/3 populations, with low- and high-threshold cells intermixed. This recruitment gradient was significantly correlated across different L4 stimulation sites, and between L4-evoked and whisker-evoked responses in vivo, indicating that a substantial component of responsiveness is independent of tuning to specific feedforward inputs. Low- and high-threshold L2/3 pyramidal cells differed in L4-evoked excitatory synaptic conductance and intrinsic excitability, including spike threshold and the likelihood of doublet spike bursts. A gradient of intrinsic excitability was observed across neurons. Cells that spiked most readily to L4 stimulation received the most synaptic excitation but had the lowest intrinsic excitability. Low- and high-threshold cells did not differ in dendritic morphology, passive membrane properties, or L4-evoked inhibitory conductance. Thus multiple gradients of physiological properties exist across L2/3 pyramidal cells, with excitatory synaptic input strength best predicting overall spiking responsiveness during network recruitment.
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