Evidence map›Paper›PMID 28009940›Full record

ArticleThe journal of gene medicine2017

An in vivo transfection system for inducible gene expression and gene silencing in murine hepatocytes.

Eric K Hubner, Christian Lechler, Birgit Kohnke-Ertel, Anne-Flore Zmoos, Julien Sage, Roland M Schmid, Ursula Ehmer

Open access · greenAbstract read
In one paragraph

Article in The journal of gene medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Gene Therapy 2017: Progress and Future Directions.Clinical and translational science · 2017
    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

7 authors at 3 institutions in 2 countries.

Eric K HubnerDepartment of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Christian LechlerDepartment of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Birgit Kohnke-ErtelDepartment of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Anne-Flore ZmoosDepartment of Pediatrics and Genetics, Stanford University School of Medicine, Stanford, California, USA.
Julien SageDepartment of Pediatrics and Genetics, Stanford University School of Medicine, Stanford, California, USA.
Roland M SchmidDepartment of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Ursula EhmerDepartment of Medicine II, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Technical University of Munich · DEKlinikum rechts der Isar · DEPediatrics and Genetics · US

Funding

Stanford Center for Clinical and Translational Education and Research (SCCTER)UL1UL1RR025744 · NCRR · STANFORD UNIVERSITY · PI GREENBERG, HARRY BERNARD · 2008 to 2011
$22.4M
The RB pathway in liver cancerR01CA114102 · NCI · STANFORD UNIVERSITY · PI SAGE, JULIEN · 2006 to 2016
$2.9M
NCI NIH HHS R01 CA114102NCRR NIH HHS UL1 RR025744
6 · The paper itself

Abstract

backgroundHydrodynamic tail vein injection (HTVI) of transposon-based integration vectors is an established system for stably transfecting mouse hepatocytes in vivo that has been successfully employed to study key questions in liver biology and cancer. Refining the vectors for transposon-mediated hepatocyte transfection will further expand the range of applications of this technique in liver research. In the present study, we report an advanced transposon-based system for manipulating gene expression in hepatocytes in vivo.

methodsTransposon-based vector constructs were generated to enable the constitutive expression of inducible Cre recombinase (CreER) together with tetracycline-inducible transgene or miR-small hairpin RNA (shRNA) expression (Tet-ON system). Transposon and transposase expression vectors were co-injected into R26R-mTmG reporter mice by HTVI. Cre-mediated gene recombination was induced by tamoxifen, followed by the administration of doxycycline to drive tetracycline-inducible gene or shRNA expression. Expression was visualized by immunofluorescence staining in livers of injected mice.

resultsAfter HTVI, Cre recombination by tamoxifen led to the expression of membrane-bound green fluorescent protein in transfected hepatocytes. Activation of inducible gene or shRNA expression was detected by immunostaining in up to one-third of transfected hepatocytes, with an efficiency dependent on the promoter driving the Tet-ON system.

conclusionsOur vector system combines Cre-lox mediated gene mutation with inducible gene expression or gene knockdown, respectively. It provides the opportunity for rapid and specific modification of hepatocyte gene expression and can be a useful tool for genetic screening approaches and analysis of target genes specifically in genetically engineered mouse models.

Indexed as

Gene ExpressionGene SilencingTransfectionAnimalsDNA Transposable ElementsDoxycyclineGene Expression RegulationGene Knockout TechniquesGene OrderGenes, ReporterGenetic VectorsHepatocytesHomologous RecombinationMicePromoter Regions, GeneticRNA, Small InterferingDNA Transposable ElementsDoxycyclineRNA, Small InterferingHTVIhydrodynamic tail vein injectioninducible gene expressionsleeping beauty transposonTet-ON system

Identifiers

PMID28009940
PMCPMC9481923
OpenAlexW2566064252

What OpenQuestion holds

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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.