Evidence map›Paper›PMID 30972540›Full record

ArticleJournal of molecular neuroscience : MN2019

Separate Gene Transfers into Pre- and Postsynaptic Neocortical Neurons Connected by mGluR5-Containing Synapses.

Aarti Nagayach, Anshuman Singh, Alfred I Geller

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Recombinant Antibodies in Basic Neuroscience Research.Current protocols in neuroscience · 2020
    Review
  2. 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 at 1 institution in 1 country.

Aarti NagayachDepartment of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, USA.
Anshuman SinghDepartment of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, USA.
Alfred I GellerDepartment of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, USA. agelle@lsuhsc.edu.ORCID http://orcid.org/0000-0001-6313-5250
Louisiana State University Health Sciences Center New Orleans · US

Funding

Targeted gene transfer across specific synapse typesR01NS086960 · NINDS · LSU HEALTH SCIENCES CENTER · PI GELLER, ALFRED I. · 2014 to 2017
$1.4M
Lions Eye Foundation 1National Institutes of Health NS086960NINDS NIH HHS R01 NS086960Research to Prevent Blindness 1
6 · The paper itself

Abstract

mGluR5-containing synapses have essential roles in synaptic plasticity, circuit physiology, and learning, and dysfunction at these synapses is implicated in specific neurological disorders. As mGluR5-containing synapses are embedded in large and complex distributed circuits containing many neuron and synapse types, it is challenging to elucidate the roles of these synapses and to develop treatments for the associated disorders. Thus, it would be advantageous to deliver different genes into pre- and postsynaptic neurons connected by a mGluR5-containing synapse. Here, we develop this capability: The first gene transfer, into the presynaptic neurons, uses standard techniques to deliver a vector that expresses a synthetic peptide neurotransmitter. This peptide neurotransmitter has three domains: a dense core vesicle sorting domain, a mGluR5-binding domain composed of a single-chain variable fragment anti-mGluR5, and the His tag. Upon release, this peptide neurotransmitter binds to mGluR5, predominately located on the postsynaptic neurons. Selective gene transfer into these neurons uses antibody-mediated, targeted gene transfer and anti-His tag antibodies, as the synthetic peptide neurotransmitter contains the His tag. For the model system, we studied the connection between neurons in two neocortical areas: postrhinal and perirhinal cortices. Targeted gene transfer was over 80% specific for mGluR5-containing synapses, but untargeted gene transfer was only ~ 15% specific for these synapses. This technology may enable studies on the roles of mGluR5-containing neurons and synapses in circuit physiology and learning and support gene therapy treatments for specific disorders that involve dysfunction at these synapses.

Indexed as

Gene Transfer TechniquesAnimalsCell LineCricetinaeGenetic VectorsMaleNeocortexNeuronsNeurotransmitter AgentsRatsRats, Long-EvansReceptor, Metabotropic Glutamate 5Recombinant ProteinsSynapsesNeurotransmitter AgentsReceptor, Metabotropic Glutamate 5Recombinant ProteinsHerpes simplex virus vectormGluR5Single-chain variable fragmentSynapseSynthetic peptide neurotransmitterTargeted gene transfer

Identifiers

PMID30972540
PMCPMC6615967
OpenAlexW2937870633

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.