Evidence map›Paper›PMID 20736420›Full record

ArticleThe Journal of physiology2010

Transgene expression and effective gene silencing in vagal afferent neurons in vivo using recombinant adeno-associated virus vectors.

M Kollarik, M J Carr, F Ru, C J A Ring, V J Hart, P Murdock, A C Myers, Y Muroi, B J Undem

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 26 citations in OpenAlex.

  1. Gut-brain communication: types of sensory nerves and mechanisms of activation.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. TRP channel functions in the gastrointestinal tract.Seminars in immunopathology · 2016
    Review
  13. Article
  14. Peripheral neural circuitry in cough.Current opinion in pharmacology · 2015
    Review
  15. Article
  16. A method of nodose ganglia injection in Sprague-Dawley rat.Journal of visualized experiments : JoVE · 2014
    Article
  17. Article
  18. Selective inhibition of vagal afferent nerve pathways regulating cough using Nav 1.7 shRNA silencing in guinea pig nodose ganglia.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

M KollarikThe Johns Hopkins School of Medicine, Baltimore, MD 21224, USA.
M J Carr
F Ru
C J A Ring
V J Hart
P Murdock
A C Myers
Y Muroi
B J Undem
Johns Hopkins University · USGlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (United States) · US

Funding

Airway Sensory NeuroexcitabilityR01HL062296 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI UNDEM, BRADLEY JOEL · 2000 to 2013
$5.0M
Activation of Nociceptors in EsophagusR01DK074480 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI KOLLARIK, MARIAN · 2007 to 2011
$1.4M
NHLBI NIH HHS HL062296NHLBI NIH HHS R01 HL062296NIDDK NIH HHS DK074480NIDDK NIH HHS R01 DK074480
6 · The paper itself

Abstract

Vagal afferent fibres innervating thoracic structures such as the respiratory tract and oesophagus are diverse, comprising several subtypes of functionally distinct C-fibres and A-fibres. Both morphological and functional studies of these nerve subtypes would be advanced by selective, effective and long-term transduction of vagal afferent neurons with viral vectors. Here we addressed the hypothesis that vagal sensory neurons can be transduced with adeno-associated virus (AAV) vectors in vivo, in a manner that would be useful for morphological assessment of nerve terminals, using enhanced green fluorescent protein (eGFP), as well as for the selective knock-down of specific genes of interest in a tissue-selective manner. We found that a direct microinjection of AAV vectors into the vagal nodose ganglia in vivo leads to selective, effective and long-lasting transduction of the vast majority of primary sensory vagal neurons without transduction of parasympathetic efferent neurons. The transduction of vagal neurons by pseudoserotype AAV2/8 vectors in vivo is sufficiently efficient such that it can be used to functionally silence TRPV1 gene expression using short hairpin RNA (shRNA). The eGFP encoded by AAV vectors is robustly transported to both the central and peripheral terminals of transduced vagal afferent neurons allowing for bright imaging of the nerve endings in living tissues and suitable for structure-function studies of vagal afferent nerve endings. Finally, the AAV2/8 vectors are efficiently taken up by the vagal nerve terminals in the visceral tissue and retrogradely transported to the cell body, allowing for tissue-specific transduction.

Indexed as

Genetic VectorsAdenoviridaeAnimalsAnimals, Genetically ModifiedGene SilencingGreen Fluorescent ProteinsGuinea PigsModels, AnimalNeurons, AfferentNodose GanglionPatch-Clamp TechniquesTRPV Cation ChannelsGreen Fluorescent ProteinsTRPV1 protein, mouseTRPV Cation Channels

Identifiers

PMID20736420
PMCPMC3002458
OpenAlexW1511493669

What OpenQuestion holds

Textmetadata
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.