Evidence map›Paper›PMID 26594154›Full record

ArticleFrontiers in neural circuits2015

Bulk regional viral injection in neonatal mice enables structural and functional interrogation of defined neuronal populations throughout targeted brain areas.

Claire E J Cheetham, Bryce D Grier, Leonardo Belluscio

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
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  6. Review
  7. Article
  8. All-or-none disconnection of pyramidal inputs onto parvalbumin-positive interneurons gates ocular dominance plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Article
  10. CCKergic Tufted Cells Differentially Drive Two Anatomically Segregated Inhibitory Circuits in the Mouse Olfactory Bulb.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Multiphoton Intravital Calcium Imaging.Current protocols in cytometry · 2018
    Article
  15. Article
  16. Article
  17. Olfactory Bulb Deep Short-Axon Cells Mediate Widespread Inhibition of Tufted Cell Apical Dendrites.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  18. Article
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

3 authors.

Claire E J CheethamNational Institute of Neurological Disorders and Stroke Bethesda, MD, USA ; Department of Biological Sciences, Carnegie Mellon University Pittsburgh, PA, USA.
Bryce D GrierNational Institute of Neurological Disorders and Stroke Bethesda, MD, USA.
Leonardo BelluscioNational Institute of Neurological Disorders and Stroke Bethesda, MD, USA.

Funding

Development and modification of neural circuitry in the mammalian olfactory bulbZIANS003002 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI BELLUSCIO, LEONARDO · 2009 to 2017
$8.4M
Development and modification of neural circuitry in the mammalian olfactory bulbZ01NS003002 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI BELLUSCIO, LEONARDO · 2003 to 2008
$2.8M
Intramural NIH HHS Z01 NS003002NINDS NIH HHS 1-ZIA-NS003002
6 · The paper itself

Abstract

The ability to label and manipulate specific cell types is central to understanding the structure and function of neuronal circuits. Here, we have developed a simple, affordable strategy for labeling of genetically defined populations of neurons throughout a targeted brain region: Bulk Regional Viral Injection (BReVI). Our strategy involves a large volume adeno-associated virus (AAV) injection in the targeted brain region of neonatal Cre driver mice. Using the mouse olfactory bulb (OB) as a model system, we tested the ability of BReVI to broadly and selectively label tufted cells, one of the two principal neuron populations of the OB, in CCK-IRES-Cre mice. BReVI resulted in labeling of neurons throughout the injected OB, with no spatial bias toward the injection site and no evidence of damage. The specificity of BReVI labeling was strikingly similar to that seen previously using immunohistochemical staining for cholecystokinin (CCK), an established tufted cell marker. Hence, the CCK-IRES-Cre line in combination with BReVI can provide an important tool for targeting and manipulation of OB tufted cells. We also found robust Cre-dependent reporter expression within three days of BReVI, which enabled us to assess developmental changes in the number and laminar distribution of OB tufted cells during the first three postnatal weeks. Furthermore, we demonstrate that BReVI permits structural and functional imaging in vivo, and can be combined with transgenic strategies to facilitate multi-color labeling of neuronal circuit components. BReVI is broadly applicable to different Cre driver lines and can be used to regionally manipulate genetically defined populations of neurons in any accessible brain region.

Indexed as

DependovirusAnimalsAnimals, NewbornBrainCell CountCholecystokininCytological TechniquesDopamineGenetic VectorsGene Transfer TechniquesImmunohistochemistryMice, TransgenicMicrogliaMicroscopy, ConfocalNeuronsOlfactory PerceptionCholecystokininDopamineadeno-associated virusbulk labelingneural circuitolfactory bulbtufted cell

Identifiers

PMID26594154
PMCPMC4633521

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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.