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1.
Nat Neurosci ; 21(11): 1583-1590, 2018 11.
Article in English | MEDLINE | ID: mdl-30349100

ABSTRACT

Animals strategically scan the environment to form an accurate perception of their surroundings. Here we investigated the neuronal representations that mediate this behavior. Ca2+ imaging and selective optogenetic manipulation during an active sensing task reveals that layer 5 pyramidal neurons in the vibrissae cortex produce a diverse and distributed representation that is required for mice to adapt their whisking motor strategy to changing sensory cues. The optogenetic perturbation degraded single-neuron selectivity and network population encoding through a selective inhibition of active dendritic integration. Together the data indicate that active dendritic integration in pyramidal neurons produces a nonlinearly mixed network representation of joint sensorimotor parameters that is used to transform sensory information into motor commands during adaptive behavior. The prevalence of the layer 5 cortical circuit motif suggests that this is a general circuit computation.


Subject(s)
Behavior, Animal/physiology , Dendrites/physiology , Neocortex/physiology , Nerve Net/physiology , Neurons/physiology , Adaptation, Psychological/physiology , Animals , Male , Mice , Somatosensory Cortex/physiology , Vibrissae/physiology
2.
J Neurophysiol ; 104(3): 1812-24, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20610791

ABSTRACT

Activity in populations of neurons is essential for cortical function including signaling of information and signal transport. Previous methods have made advances in recording activity from many neurons but have both technical and analytical limitations. Here we present an optical method, dithered random-access functional calcium imaging, to record somatic calcium signals from up to 100 neurons, in vitro and in vivo. We further developed a maximum-likelihood deconvolution algorithm to detect spikes and precise spike timings from the recorded calcium fluorescence signals. Spike detection efficiency and spike timing detection was determined in acute slices of juvenile mice. The results indicate that the combination of the two methods detected precise spiking activity from unbiased and spatially distributed populations of neurons in acute slices with high efficiency of spike detection (>97%), low rate of false positives (0.0023 spikes/s), and high temporal precision. The results further indicate that there is only a small window of excitation intensities where high spike detection can be achieved consistently.


Subject(s)
Action Potentials/physiology , Neurons/physiology , Voltage-Sensitive Dye Imaging/methods , Voltage-Sensitive Dye Imaging/standards , Animals , Animals, Newborn , Calcium Signaling/physiology , Mice , Mice, Inbred C57BL , Microscopy, Confocal/methods , Microscopy, Confocal/standards , Random Allocation , Rats , Rats, Sprague-Dawley , Time Factors
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