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1.
Nature ; 593(7860): 558-563, 2021 05.
Article in English | MEDLINE | ID: mdl-33953395

ABSTRACT

Odours are transported in turbulent plumes, which result in rapid concentration fluctuations1,2 that contain rich information about the olfactory scenery, such as the composition and location of an odour source2-4. However, it is unclear whether the mammalian olfactory system can use the underlying temporal structure to extract information about the environment. Here we show that ten-millisecond odour pulse patterns produce distinct responses in olfactory receptor neurons. In operant conditioning experiments, mice discriminated temporal correlations of rapidly fluctuating odours at frequencies of up to 40 Hz. In imaging and electrophysiological recordings, such correlation information could be readily extracted from the activity of mitral and tufted cells-the output neurons of the olfactory bulb. Furthermore, temporal correlation of odour concentrations5 reliably predicted whether odorants emerged from the same or different sources in naturalistic environments with complex airflow. Experiments in which mice were trained on such tasks and probed using synthetic correlated stimuli at different frequencies suggest that mice can use the temporal structure of odours to extract information about space. Thus, the mammalian olfactory system has access to unexpectedly fast temporal features in odour stimuli. This endows animals with the capacity to overcome key behavioural challenges such as odour source separation5, figure-ground segregation6 and odour localization7 by extracting information about space from temporal odour dynamics.


Subject(s)
Olfactory Bulb/cytology , Olfactory Receptor Neurons/physiology , Smell/physiology , Air Movements , Animals , Behavior, Animal , Conditioning, Operant , Male , Mice , Mice, Inbred C57BL , Models, Neurological , Odorants , Patch-Clamp Techniques , Spatial Behavior , Time Factors
2.
PLoS Comput Biol ; 18(1): e1009808, 2022 01.
Article in English | MEDLINE | ID: mdl-35100264

ABSTRACT

Sensory processing is hard because the variables of interest are encoded in spike trains in a relatively complex way. A major goal in studies of sensory processing is to understand how the brain extracts those variables. Here we revisit a common encoding model in which variables are encoded linearly. Although there are typically more variables than neurons, this problem is still solvable because only a small number of variables appear at any one time (sparse prior). However, previous solutions require all-to-all connectivity, inconsistent with the sparse connectivity seen in the brain. Here we propose an algorithm that provably reaches the MAP (maximum a posteriori) inference solution, but does so using sparse connectivity. Our algorithm is inspired by the circuit of the mouse olfactory bulb, but our approach is general enough to apply to other modalities. In addition, it should be possible to extend it to nonlinear encoding models.


Subject(s)
Algorithms , Sensory Receptor Cells/physiology , Action Potentials/physiology , Animals , Mice , Nonlinear Dynamics
3.
J Neurosci ; 32(3): 787-98, 2012 Jan 18.
Article in English | MEDLINE | ID: mdl-22262877

ABSTRACT

Acoustic communication in drosophilid flies is based on the production and perception of courtship songs, which facilitate mating. Despite decades of research on courtship songs and behavior in Drosophila, central auditory responses have remained uncharacterized. In this study, we report on intracellular recordings from central neurons that innervate the Drosophila antennal mechanosensory and motor center (AMMC), the first relay for auditory information in the fly brain. These neurons produce graded-potential (nonspiking) responses to sound; we compare recordings from AMMC neurons to extracellular recordings of the receptor neuron population [Johnston's organ neurons (JONs)]. We discover that, while steady-state response profiles for tonal and broadband stimuli are significantly transformed between the JON population in the antenna and AMMC neurons in the brain, transient responses to pulses present in natural stimuli (courtship song) are not. For pulse stimuli in particular, AMMC neurons simply low-pass filter the receptor population response, thus preserving low-frequency temporal features (such as the spacing of song pulses) for analysis by postsynaptic neurons. We also compare responses in two closely related Drosophila species, Drosophila melanogaster and Drosophila simulans, and find that pulse song responses are largely similar, despite differences in the spectral content of their songs. Our recordings inform how downstream circuits may read out behaviorally relevant information from central neurons in the AMMC.


Subject(s)
Animal Communication , Brain/cytology , Courtship , Sensory Receptor Cells/physiology , Acoustic Stimulation/methods , Acoustics , Action Potentials/genetics , Action Potentials/physiology , Animals , Animals, Genetically Modified , Auditory Pathways/physiology , Auditory Perception , Biophysics , Brain/physiology , Drosophila , Drosophila Proteins , Electric Stimulation , Female , Fourier Analysis , Green Fluorescent Proteins/genetics , Male , Patch-Clamp Techniques , Reaction Time , Sense Organs/cytology , Sense Organs/physiology , Sound , Sound Spectrography
4.
Elife ; 82019 05 21.
Article in English | MEDLINE | ID: mdl-31112127

ABSTRACT

Most sensory systems are organized into parallel neuronal pathways that process distinct aspects of incoming stimuli. In the insect olfactory system, second order projection neurons target both the mushroom body, required for learning, and the lateral horn (LH), proposed to mediate innate olfactory behavior. Mushroom body neurons form a sparse olfactory population code, which is not stereotyped across animals. In contrast, odor coding in the LH remains poorly understood. We combine genetic driver lines, anatomical and functional criteria to show that the Drosophila LH has ~1400 neurons and >165 cell types. Genetically labeled LHNs have stereotyped odor responses across animals and on average respond to three times more odors than single projection neurons. LHNs are better odor categorizers than projection neurons, likely due to stereotyped pooling of related inputs. Our results reveal some of the principles by which a higher processing area can extract innate behavioral significance from sensory stimuli.


Subject(s)
Drosophila , Olfactory Cortex/anatomy & histology , Olfactory Cortex/physiology , Olfactory Perception , Animals
5.
Neuron ; 80(5): 1246-62, 2013 Dec 04.
Article in English | MEDLINE | ID: mdl-24210905

ABSTRACT

Natural odors are usually mixtures; yet, humans and animals can experience them as unitary percepts. Olfaction also enables stimulus categorization and generalization. We studied how these computations are performed with the responses of 168 locust antennal lobe projection neurons (PNs) to varying mixtures of two monomolecular odors, and of 174 PNs and 209 mushroom body Kenyon cells (KCs) to mixtures of up to eight monomolecular odors. Single-PN responses showed strong hypoadditivity and population trajectories clustered by odor concentration and mixture similarity. KC responses were much sparser on average than those of PNs and often signaled the presence of single components in mixtures. Linear classifiers could read out the responses of both populations in single time bins to perform odor identification, categorization, and generalization. Our results suggest that odor representations in the mushroom body may result from competing optimization constraints to facilitate memorization (sparseness) while enabling identification, classification, and generalization.


Subject(s)
Neurons/physiology , Olfactory Pathways/cytology , Smell/physiology , Action Potentials/physiology , Animals , Arthropod Antennae/physiology , Bayes Theorem , Grasshoppers , Linear Models , Models, Neurological , Mushroom Bodies/cytology , Neural Pathways/physiology , Neurons/classification , Odorants , ROC Curve , Reaction Time/physiology , Time Factors
6.
Neuron ; 67(6): 903-5, 2010 Sep 23.
Article in English | MEDLINE | ID: mdl-20869588

ABSTRACT

Recent work established the spread of interglomerular excitation in the Drosophila antennal lobe. Two papers in this issue of Neuron, by Huang et al. and Yaksi and Wilson, show that cholinergic krasavietz local interneurons are a major substrate for this spread of excitation, predominantly via electrical coupling.

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