Evidence map›Paper›PMID 15005815›Full record

ArticleBMC neuroscience2004

Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors.

Bushra Y Ahmed, Sridhara Chakravarthy, Ruben Eggers, Wim T J M C Hermens, Jing Ying Zhang, Simone P Niclou, Christiaan Levelt, Fred Sablitzky, Patrick N Anderson, A R Lieberman and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

54 citing papers in PubMed, 110 citations in OpenAlex.

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  15. β1-Integrins in the Developing Orbitofrontal Cortex Are Necessary for Expectancy Updating in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
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  19. Optogenetic and chemogenetic techniques for neurogastroenterology.Nature reviews. Gastroenterology & hepatology · 2018
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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

11 authors at 6 institutions in 2 countries.

Bushra Y AhmedDepartment of Anatomy and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK. Bushra.Ahmed@ucl.ac.uk
Sridhara Chakravarthy
Ruben Eggers
Wim T J M C Hermens
Jing Ying Zhang
Simone P Niclou
Christiaan Levelt
Fred Sablitzky
Patrick N Anderson
A R Lieberman
Joost Verhaagen
Netherlands Institute for Neuroscience · NLUniversity College London · GBQueen's Medical Centre · GBRoyal Academy of Art · NLRoyal Netherlands Academy of Arts and Sciences · NLUniversity of Nottingham · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundInactivating genes in vivo is an important technique for establishing their function in the adult nervous system. Unfortunately, conventional knockout mice may suffer from several limitations including embryonic or perinatal lethality and the compensatory regulation of other genes. One approach to producing conditional activation or inactivation of genes involves the use of Cre recombinase to remove loxP-flanked segments of DNA. We have studied the effects of delivering Cre to the hippocampus and neocortex of adult mice by injecting replication-deficient adeno-associated virus (AAV) and lentiviral (LV) vectors into discrete regions of the forebrain.

resultsRecombinant AAV-Cre, AAV-GFP (green fluorescent protein) and LV-Cre-EGFP (enhanced GFP) were made with the transgene controlled by the cytomegalovirus promoter. Infecting 293T cells in vitro with AAV-Cre and LV-Cre-EGFP resulted in transduction of most cells as shown by GFP fluorescence and Cre immunoreactivity. Injections of submicrolitre quantities of LV-Cre-EGFP and mixtures of AAV-Cre with AAV-GFP into the neocortex and hippocampus of adult Rosa26 reporter mice resulted in strong Cre and GFP expression in the dentate gyrus and moderate to strong labelling in specific regions of the hippocampus and in the neocortex, mainly in neurons. The pattern of expression of Cre and GFP obtained with AAV and LV vectors was very similar. X-gal staining showed that Cre-mediated recombination had occurred in neurons in the same regions of the brain, starting at 3 days post-injection. No obvious toxic effects of Cre expression were detected even after four weeks post-injection.

conclusionAAV and LV vectors are capable of delivering Cre to neurons in discrete regions of the adult mouse brain and producing recombination.

Indexed as

Gene Transfer TechniquesAnimalsCell LineDependovirusGene ExpressionGenes, ReporterGenetic VectorsGreen Fluorescent ProteinsHippocampusIntegrasesLentivirusLuminescent ProteinsMiceMice, TransgenicNeocortexNeuronsCre recombinaseGreen Fluorescent ProteinsIntegrasesLuminescent ProteinsRecombinant ProteinsViral Proteins

Identifiers

PMID15005815
PMCPMC343275
OpenAlexW2130704258

What OpenQuestion holds

Textmetadata
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.