Evidence map›Paper›PMID 19144149›Full record

ArticleBMC neuroscience2009

Lentivirus-mediated transgene delivery to the hippocampus reveals sub-field specific differences in expression.

Lenneke W A van Hooijdonk, Muhammad Ichwan, Thomas F Dijkmans, Theo G Schouten, Marijke W A de Backer, Roger A H Adan, Fons J Verbeek, Erno Vreugdenhil, Carlos P Fitzsimons

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

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  17. Lentiviral transduction of neuronal cells.Methods in molecular biology (Clifton, N.J.) · 2013
    Article
  18. Article
  19. Article
  20. Structural plasticity and hippocampal function.Annual review of psychology · 2010
    Review
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

9 authors at 3 institutions in 1 country.

Lenneke W A van HooijdonkMedical Pharmacology Department, Leiden/Amsterdam Center for Drug Research, Leiden University Medical Center, Leiden University, the Netherlands. l.van.hooijdonk@lacdr.leidenuniv.nl
Muhammad Ichwan
Thomas F Dijkmans
Theo G Schouten
Marijke W A de Backer
Roger A H Adan
Fons J Verbeek
Erno Vreugdenhil
Carlos P Fitzsimons
Leiden University Medical Center · NLUniversity Medical Center Utrecht · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the adult hippocampus, the granule cell layer of the dentate gyrus is a heterogeneous structure formed by neurons of different ages, morphologies and electrophysiological properties. Retroviral vectors have been extensively used to transduce cells of the granule cell layer and study their inherent properties in an intact brain environment. In addition, lentivirus-based vectors have been used to deliver transgenes to replicative and non-replicative cells as well, such as post mitotic neurons of the CNS. However, only few studies have been dedicated to address the applicability of these widespread used vectors to hippocampal cells in vivo. Therefore, the aim of this study was to extensively characterize the cell types that are effectively transduced in vivo by VSVg-pseudotyped lentivirus-based vectors in the hippocampus dentate gyrus.

resultsIn the present study we used Vesicular Stomatitis Virus G glycoprotein-pseudotyped lentivirual vectors to express EGFP from three different promoters in the mouse hippocampus. In contrast to lentiviral transduction of pyramidal cells in CA1, we identified sub-region specific differences in transgene expression in the granule cell layer of the dentate gyrus. Furthermore, we characterized the cell types transduced by these lentiviral vectors, showing that they target primarily neuronal progenitor cells and immature neurons present in the sub-granular zone and more immature layers of the granule cell layer.

conclusionOur observations suggest the existence of intrinsic differences in the permissiveness to lentiviral transduction among various hippocampal cell types. In particular, we show for the first time that mature neurons of the granule cell layer do not express lentivirus-delivered transgenes, despite successful expression in other hippocampal cell types. Therefore, amongst hippocampal granule cells, only adult-generated neurons are target for lentivirus-mediated transgene delivery. These properties make lentiviral vectors excellent systems for overexpression or knockdown of genes in neuronal progenitor cells, immature neurons and adult-generated neurons of the mouse hippocampus in vivo.

Indexed as

Gene ExpressionGenetic VectorsTransduction, GeneticAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2Green Fluorescent ProteinsHippocampusLentivirusMaleMembrane GlycoproteinsMiceMice, Inbred C57BLNeuronsPromoter Regions, GeneticRatsRats, WistarCalcium-Calmodulin-Dependent Protein Kinase Type 2enhanced green fluorescent proteinG protein, vesicular stomatitis virusGreen Fluorescent ProteinsMembrane GlycoproteinsRNA, MessengerSynapsinsViral Envelope Proteins

Identifiers

PMID19144149
PMCPMC2647928
OpenAlexW2122366132

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.