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1.
Cell Rep ; 22(13): 3534-3547, 2018 03 27.
Article in English | MEDLINE | ID: mdl-29590621

ABSTRACT

Rodents explore their environment with an array of whiskers, inducing complex patterns of whisker deflections. Cortical neuronal networks can extract global properties of tactile scenes. In the primary somatosensory cortex, the information relative to the global direction of a spatiotemporal sequence of whisker deflections can be extracted at the single neuron level. To further understand how the cortical network integrates multi-whisker inputs, we imaged and recorded the mouse barrel cortex activity evoked by sequences of multi-whisker deflections generating global motions in different directions. A majority of barrel-related cortical columns show a direction preference for global motions with an overall preference for caudo-ventral directions. Responses to global motions being highly sublinear, the identity of the first deflected whiskers is highly salient but does not seem to determine the global direction preference. Our results further demonstrate that the global direction preference is spatially organized throughout the barrel cortex at a supra-columnar scale.


Subject(s)
Neurons/physiology , Somatosensory Cortex/physiology , Vibrissae/physiology , Animals , Female , Male , Mice , Mice, Inbred C57BL , Physical Stimulation/methods , Somatosensory Cortex/cytology
2.
J Neurosci Methods ; 263: 145-54, 2016 Apr 01.
Article in English | MEDLINE | ID: mdl-26384542

ABSTRACT

BACKGROUND: The rodent barrel cortex is a widely used model to study the cortical processing of tactile sensory information. It is notable by the cytoarchitecture of its layer IV, which contains distinguishable structural units called barrels that can be considered as anatomical landmarks of the functional columnar organization of the cerebral cortex. To study sensory integration in the barrel cortex it is therefore essential to map recorded functional data onto the underlying barrel topography, which can be reconstructed from the post hoc alignment of tangential brain slices stained for cytochrome oxidase. NEW METHOD: This article presents an automated workflow to perform the registration of histological slices of the barrel cortex followed by the 2-D reconstruction of the barrel map from the registered slices. The registration of two successive slices is obtained by computing a rigid transformation to align sets of detected blood vessel cross-sections. This is achieved by using a robust variant of the classical iterative closest point method. A single fused image of the barrel field is then generated by computing a nonlinear merging of the gradients from the registered images. COMPARISON WITH EXISTING METHODS: This novel anatomo-functional mapping tool leads to a substantial gain in time and precision compared to conventional manual methods. It provides a flexible interface for the user with only a few parameters to tune. CONCLUSIONS: We demonstrate here the usefulness of the method for voltage sensitive dye imaging of the mouse barrel cortex. The method could also benefit other experimental approaches and model species.


Subject(s)
Brain Mapping , Somatosensory Cortex/anatomy & histology , Somatosensory Cortex/physiology , Workflow , Animals , Blood Vessels/anatomy & histology , Mice , Numerical Analysis, Computer-Assisted , Physical Stimulation , Vibrissae/innervation , Voltage-Sensitive Dye Imaging
3.
J Neurophysiol ; 114(1): 332-40, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25972583

ABSTRACT

Low-threshold voltage-activated calcium conductances (LT-VACCs) play a substantial role in shaping the electrophysiological attributes of neurites. We have investigated how these conductances affect synaptic integration in a premotor nonspiking (NS) neuron of the leech nervous system. These cells exhibit an extensive neuritic tree, do not fire Na(+)-dependent spikes, but express an LT-VACC that was sensitive to 250 µM Ni(2+) and 100 µM NNC 55-0396 (NNC). NS neurons responded to excitation of mechanosensory pressure neurons with depolarizing responses for which amplitude was a linear function of the presynaptic firing frequency. NNC decreased these synaptic responses and abolished the concomitant widespread Ca(2+) signals. Coherent with the interpretation that the LT-VACC amplified signals at the postsynaptic level, this conductance also amplified the responses of NS neurons to direct injection of sinusoidal current. Synaptic amplification thus is achieved via a positive feedback in which depolarizing signals activate an LT-VACC that, in turn, boosts these signals. The wide distribution of LT-VACC could support the active propagation of depolarizing signals, turning the complex NS neuritic tree into a relatively compact electrical compartment.


Subject(s)
Action Potentials/physiology , Calcium Channels/metabolism , Neurons/physiology , Synapses/physiology , Action Potentials/drug effects , Animals , Calcium/metabolism , Calcium Channel Blockers/pharmacology , Calcium Channels/drug effects , Leeches , Neurons/drug effects , Patch-Clamp Techniques , Synapses/drug effects , Voltage-Sensitive Dye Imaging
4.
J Neurophysiol ; 109(3): 711-20, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23155168

ABSTRACT

Signal processing in neuritic trees is ruled by the concerted action of passive and active membrane properties that, together, determine the degree of electrical compartmentalization of these trees. We analyzed how active properties modulate spatial propagation of graded signals in a pair of nonspiking (NS) neurons of the leech. NS neurons present a very extensive neuritic tree that mediates the interaction with all the excitatory motoneurons in leech ganglia. NS cells express voltage-activated Ca(2+) conductances (VACCs) that, under certain experimental conditions, evoke low-threshold spikes. We studied the distribution of calcium transients in NS neurons loaded with fluorescent calcium probes in response to low-threshold spikes, electrical depolarizing pulses, and synaptic inputs. The three types of stimuli evoked calcium transients of similar characteristics in the four main branches of the neuron. The magnitude of the calcium transients evoked by electrical pulses was a graded function of the change in NS membrane potential and depended on the baseline potential level. The underlying VACCs were partially inactivated at rest and strongly inactivated at -20 mV. Stimulation of mechanosensory pressure cells evoked calcium transients in NS neurons whose amplitude was a linear function of the amplitude of the postsynaptic response. The results evidenced that VACCs aid an efficient propagation of graded signals, turning the vast neuritic tree of NS cells into an electrically compact structure.


Subject(s)
Action Potentials , Motor Neurons/physiology , Synaptic Potentials , Animals , Calcium/metabolism , Calcium Channels/physiology , Ganglia, Invertebrate/cytology , Ganglia, Invertebrate/physiology , Leeches , Mechanoreceptors/physiology , Mechanotransduction, Cellular
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