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Spinal nociceptive circuit analysis with recombinant adeno‐associated viruses: the impact of serotypes and promoters

Overview of attention for article published in Journal of Neurochemistry, August 2017
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (73rd percentile)
  • Good Attention Score compared to outputs of the same age and source (72nd percentile)

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Article details
Title
Spinal nociceptive circuit analysis with recombinant adeno‐associated viruses: the impact of serotypes and promoters
Published in
Journal of Neurochemistry, August 2017
DOI 10.1111/jnc.14124
Pubmed ID
Authors
Abstract

Recombinant adeno-associated virus (rAAV) vector-mediated gene transfer into genetically defined neuron subtypes has become a powerful tool to study the neuroanatomy of neuronal circuits in the brain and to unravel their functions. More recently this methodology has also become popular for the analysis of spinal cord circuits. To date a variety of naturally occurring AAV serotypes and genetically modified capsid variants are available but transduction efficiency in spinal neurons, target selectivity and the ability for retrograde tracing are only incompletely characterized. Here, we have compared the transduction efficiency of seven commonly used AAV serotypes after intraspinal injection. We specifically analyzed local transduction of different types of dorsal horn neurons, and retrograde transduction of dorsal root ganglia (DRG) neurons and of neurons in the rostral ventromedial medulla (RVM) and the somatosensory cortex (S1). Our results show that most of the tested rAAV vectors have similar transduction efficiency in spinal neurons. All serotypes analyzed were also able to transduce DRG neurons and descending RVM and S1 neurons via their spinal axon terminals. When comparing the commonly used rAAV serotypes to the recently developed serotype 2 capsid variant rAAV2retro, a >20-fold increase in transduction efficiency of descending supraspinal neurons was observed. Conversely, transgene expression in retrogradely transduced neurons was strongly reduced when the human synapsin 1 (hSyn1) promoter was used instead of the strong ubiquitous CAG or CMV promoter fragments. We conclude that the use of AAV2retro greatly increases transduction of neurons connected to the spinal cord via their axon terminals, while the hSyn1 promoter can be used to minimize transgene expression in retrogradely connected neurons of the DRG or brainstem. This article is protected by copyright. All rights reserved.

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X Demographics

X Demographics

The data shown below were collected from the profiles of 8 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 76 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Unknown 76 100%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 18 24%
Student > Ph. D. Student 12 16%
Student > Doctoral Student 10 13%
Student > Master 6 8%
Student > Bachelor 4 5%
Other 10 13%
Unknown 16 21%
Readers by discipline
Readers by discipline Count As %
Neuroscience 36 47%
Agricultural and Biological Sciences 10 13%
Medicine and Dentistry 7 9%
Biochemistry, Genetics and Molecular Biology 3 4%
Veterinary Science and Veterinary Medicine 1 1%
Other 1 1%
Unknown 18 24%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 7. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 07 September 2021.
All research outputs
#5,871,712
of 27,265,018 outputs
Outputs from Journal of Neurochemistry
#1,567
of 8,038 outputs
Outputs of similar age
#86,994
of 333,513 outputs
Outputs of similar age from Journal of Neurochemistry
#17
of 62 outputs
Altmetric has tracked 27,265,018 research outputs across all sources so far. Compared to these this one has done well and is in the 78th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 8,038 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 5.9. This one has done well, scoring higher than 80% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 333,513 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 73% of its contemporaries.
We're also able to compare this research output to 62 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 72% of its contemporaries.