Evidence map›Paper›PMID 26182988›Full record

ArticleNeurobiology of learning and memory2015

Viral delivery of shRNA to amygdala neurons leads to neurotoxicity and deficits in Pavlovian fear conditioning.

Christopher A de Solis, Roopashri Holehonnur, Anwesha Banerjee, Jonathan A Luong, Srihari K Lella, Anthony Ho, Bahram Pahlavan, Jonathan E Ploski

Abstract read
In one paragraph

Article in Neurobiology of learning and memory, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

8 authors.

Christopher A de SolisSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Roopashri HolehonnurSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Anwesha BanerjeeSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Jonathan A LuongSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Srihari K LellaSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Anthony HoSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Bahram PahlavanSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States.
Jonathan E PloskiSchool of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, United States. Electronic address: Jonathan.Ploski@UTDallas.edu.

Funding

Molecular Mechanisms of Reconsolidation BoundariesR21MH096202 · NIMH · UNIVERSITY OF TEXAS DALLAS · PI PLOSKI, JONATHAN E · 2012 to 2013
$412k
Optimization of Adeno-Associated Virus for the Study of Amygdala Dependent LearniR03MH100650 · NIMH · UNIVERSITY OF TEXAS DALLAS · PI PLOSKI, JONATHAN E · 2013 to 2014
$153k
NIMH NIH HHS R03 MH100650NIMH NIH HHS R21 MH096202PHS HHS RMH096202APHS HHS RMH100650A
6 · The paper itself

Abstract

The use of viral vector technology to deliver short hairpin RNAs (shRNAs) to cells of the nervous system of many model organisms has been widely utilized by neuroscientists to study the influence of genes on behavior. However, there have been numerous reports that delivering shRNAs to the nervous system can lead to neurotoxicity. Here we report the results of a series of experiments where adeno-associated viruses (AAV), that were engineered to express shRNAs designed to target known plasticity associated genes (i.e. Arc, Egr1 and GluN2A) or control shRNAs that were designed not to target any rat gene product for depletion, were delivered to the rat basal and lateral nuclei of the amygdala (BLA), and auditory Pavlovian fear conditioning was examined. In our first set of experiments we found that animals that received AAV (3.16E13-1E13 GC/mL; 1 μl/side), designed to knockdown Arc (shArc), or control shRNAs targeting either luciferase (shLuc), or nothing (shCntrl), exhibited impaired fear conditioning compared to animals that received viruses that did not express shRNAs. Notably, animals that received shArc did not exhibit differences in fear conditioning compared to animals that received control shRNAs despite gene knockdown of Arc. Viruses designed to harbor shRNAs did not induce obvious morphological changes to the cells/tissue of the BLA at any dose of virus tested, but at the highest dose of shRNA virus examined (3.16E13 GC/mL; 1 μl/side), a significant increase in microglia activation occurred as measured by an increase in IBA1 immunoreactivity. In our final set of experiments we infused viruses into the BLA at a titer of (1.60E+12 GC/mL; 1 μl/side), designed to express shArc, shLuc, shCntrl or shRNAs designed to target Egr1 (shEgr1), or GluN2A (shGluN2A), or no shRNA, and found that all groups exhibited impaired fear conditioning compared to the group which received a virus that did not express an shRNA. The shEgr1 and shGluN2A groups exhibited gene knockdown of Egr1 and GluN2A compared to the other groups examined respectively, but Arc was not knocked down in the shArc group under these conditions. Differences in fear conditioning among the shLuc, shCntrl, shArc and shEgr1 groups were not detected under these circumstances; however, the shGluN2A group exhibited significantly impaired fear conditioning compared to most of the groups, indicating that gene specific deficits in fear conditioning could be observed utilizing viral mediated delivery of shRNA. Collectively, these data indicate that viral mediated shRNA expression was toxic to neurons in vivo, under all viral titers examined and this toxicity in some cases may be masking gene specific changes in learning. Therefore, the use of this technology in behavioral neuroscience warrants a heightened level of careful consideration and potential methods to alleviate shRNA induced toxicity are discussed.

Indexed as

AmygdalaAnimalsConditioning, ClassicalCytoskeletal ProteinsDependovirusEarly Growth Response Protein 1FearGene Knockdown TechniquesGenetic VectorsMaleNerve Tissue ProteinsNeuronsProtein SubunitsRatsRats, Sprague-DawleyRNA, Small Interferingactivity regulated cytoskeletal-associated proteinCytoskeletal ProteinsEarly Growth Response Protein 1Egr1 protein, ratNerve Tissue ProteinsProtein SubunitsRNA, Small InterferingAAVAmygdalaFear conditioningRNA interferenceshRNAViral

Identifiers

PMID26182988
PMCPMC4568141

What OpenQuestion holds

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Registered trials

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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.