Evidence map›Paper›PMID 23516293›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Optical dissection of odor information processing in vivo using GCaMPs expressed in specified cell types of the olfactory bulb.

Matt Wachowiak, Michael N Economo, Marta Díaz-Quesada, Daniela Brunert, Daniel W Wesson, John A White, Markus Rothermel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
5.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 134 citations in OpenAlex.

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31 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Matt WachowiakDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132, USA. matt.wachowiak@utah.edu
Michael N Economo
Marta Díaz-Quesada
Daniela Brunert
Daniel W Wesson
John A White
Markus Rothermel
Allen Institute for Brain Science · USBoston University · USUniversity of Utah · US

Funding

Dynamics of Glomerular Coding in the Olfactory BulbR01DC006441 · NIDCD · UNIVERSITY OF UTAH · PI WACHOWIAK, DALE M · 2004 to 2018
$4.9M
The Functional Organization of Inhibition in the Olfactory Bulb In VivoF32DC012718 · NIDCD · UNIVERSITY OF UTAH · PI ECONOMO, MICHAEL NICHOLAS · 2012 to 2013
$79k
NIDCD NIH HHS 1F32DC012718-01NIDCD NIH HHS 2DC012718NIDCD NIH HHS DC06441NIDCD NIH HHS F32 DC012718NIDCD NIH HHS R01 DC006441
6 · The paper itself

Abstract

Understanding central processing requires precise monitoring of neural activity across populations of identified neurons in the intact brain. In the present study, we used recently optimized variants of the genetically encoded calcium sensor GCaMP (GCaMP3 and GCaMPG5G) to image activity among genetically and anatomically defined neuronal populations in the olfactory bulb (OB), including two types of GABAergic interneurons (periglomerular [PG] and short axon [SA] cells) and OB output neurons (mitral/tufted [MT] cells) projecting to the piriform cortex. We first established that changes in neuronal spiking can be related accurately to GCaMP fluorescence changes via a simple quantitative relationship over a large dynamic range. We next used in vivo two-photon imaging from individual neurons and epifluorescence signals reflecting population-level activity to investigate the spatiotemporal representation of odorants across these neuron types in anesthetized and awake mice. Under anesthesia, individual PG and SA cells showed temporally simple responses and little spontaneous activity, whereas MT cells were spontaneously active and showed diverse temporal responses. At the population level, response patterns of PG, SA, and MT cells were surprisingly similar to those imaged from sensory inputs, with shared odorant-specific topography across the dorsal OB and inhalation-coupled temporal dynamics. During wakefulness, PG and SA cell responses increased in magnitude but remained temporally simple, whereas those of MT cells changed to complex spatiotemporal patterns reflecting restricted excitation and widespread inhibition. These results suggest multiple circuit elements with distinct roles in transforming odor representations in the OB and provide a framework for further study of early olfactory processing using optical and genetic tools.

Indexed as

Action PotentialsAnesthesiaAnimalsBrain MappingCalcium SignalingDissectionGenes, ReporterIntegrasesInterneuronsMiceMice, TransgenicMicroscopy, Fluorescence, MultiphotonOdorantsOlfactory BulbOlfactory Receptor NeuronsOrgan Culture TechniquesCre recombinaseIntegrases

Identifiers

PMID23516293
PMCPMC3690468
OpenAlexW2159807814

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.