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Reorganization of cortical population activity imaged throughout long-term sensory deprivation
by
Weber, Bruno
, Haiss, Florent
, Lütcke, Henry
, Kügler, Sebastian
, Margolis, David J
, Schulz, Kristina
, Hasan, Mazahir T
, Helmchen, Fritjof
in
631/378/2591
/ 631/378/2620
/ Action Potentials - physiology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain Mapping
/ Calcium - metabolism
/ Cerebral Cortex - cytology
/ Computer Simulation
/ Female
/ Gene Expression Regulation
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Biological
/ Neurobiology
/ Neurons - physiology
/ Neuropil - metabolism
/ Neuroplasticity
/ Neurosciences
/ Optics and Photonics
/ Physical Stimulation
/ Sensory deprivation
/ Sensory Deprivation - physiology
/ Synapsins - genetics
/ Synapsins - metabolism
/ Time Factors
/ Transduction, Genetic
/ Vibrissae - innervation
2012
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Reorganization of cortical population activity imaged throughout long-term sensory deprivation
by
Weber, Bruno
, Haiss, Florent
, Lütcke, Henry
, Kügler, Sebastian
, Margolis, David J
, Schulz, Kristina
, Hasan, Mazahir T
, Helmchen, Fritjof
in
631/378/2591
/ 631/378/2620
/ Action Potentials - physiology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain Mapping
/ Calcium - metabolism
/ Cerebral Cortex - cytology
/ Computer Simulation
/ Female
/ Gene Expression Regulation
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Biological
/ Neurobiology
/ Neurons - physiology
/ Neuropil - metabolism
/ Neuroplasticity
/ Neurosciences
/ Optics and Photonics
/ Physical Stimulation
/ Sensory deprivation
/ Sensory Deprivation - physiology
/ Synapsins - genetics
/ Synapsins - metabolism
/ Time Factors
/ Transduction, Genetic
/ Vibrissae - innervation
2012
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Reorganization of cortical population activity imaged throughout long-term sensory deprivation
by
Weber, Bruno
, Haiss, Florent
, Lütcke, Henry
, Kügler, Sebastian
, Margolis, David J
, Schulz, Kristina
, Hasan, Mazahir T
, Helmchen, Fritjof
in
631/378/2591
/ 631/378/2620
/ Action Potentials - physiology
/ Animal Genetics and Genomics
/ Animals
/ Behavioral Sciences
/ Biological Techniques
/ Biomedicine
/ Brain Mapping
/ Calcium - metabolism
/ Cerebral Cortex - cytology
/ Computer Simulation
/ Female
/ Gene Expression Regulation
/ Luminescent Proteins - genetics
/ Luminescent Proteins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Models, Biological
/ Neurobiology
/ Neurons - physiology
/ Neuropil - metabolism
/ Neuroplasticity
/ Neurosciences
/ Optics and Photonics
/ Physical Stimulation
/ Sensory deprivation
/ Sensory Deprivation - physiology
/ Synapsins - genetics
/ Synapsins - metabolism
/ Time Factors
/ Transduction, Genetic
/ Vibrissae - innervation
2012
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Reorganization of cortical population activity imaged throughout long-term sensory deprivation
Journal Article
Reorganization of cortical population activity imaged throughout long-term sensory deprivation
2012
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Overview
The authors explore how sensory maps are reshaped by experience
in vivo
, using chronic two-photon calcium imaging to follow whisker-evoked activity of individual layer 2/3 neurons in adult mouse barrel cortex over weeks. By first measuring activity with whiskers intact and then with continued trimming of all but one whisker, they describe how the redistribution of population activity underlies large-scale cortical remapping.
Sensory maps are reshaped by experience. It is unknown how map plasticity occurs
in vivo
in functionally diverse neuronal populations because activity of the same cells has not been tracked over long time periods. Here we used repeated two-photon imaging of a genetic calcium indicator to measure whisker-evoked responsiveness of the same layer 2/3 neurons in adult mouse barrel cortex over weeks, first with whiskers intact, then during continued trimming of all but one whisker. Across the baseline period, neurons displayed heterogeneous yet stable responsiveness. During sensory deprivation, responses to trimmed whisker stimulation globally decreased, whereas responses to spared whisker stimulation increased for the least active neurons and decreased for the most active neurons. These findings suggest that recruitment of inactive, 'silent' neurons is part of a convergent redistribution of population activity underlying sensory map plasticity. Sensory-driven responsiveness is a key property controlling experience-dependent activity changes in individual neurons.
Publisher
Nature Publishing Group US,Nature Publishing Group
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