Evidence map›Paper›PMID 11726636›Full record

ArticleInvestigative ophthalmology & visual science2001

Gene transfer mediated by recombinant baculovirus into mouse eye.

F Haeseleer, Y Imanishi, D A Saperstein, K Palczewski

Open access · greenAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2001. 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
1.3field-weighted citation impact, top 21% 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, 51 citations in OpenAlex.

  1. Article
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  6. Review
  7. Review
  8. Article
  9. Baculovirus: an insect-derived vector for diverse gene transfer applications.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Review
  10. Screening of complement inhibitors: shielded baculoviruses increase the safety and efficacy of gene delivery.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Article
  11. Article
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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

4 authors at 1 institution in 1 country.

F HaeseleerDepartment of Ophthalmology, University of Washington, 1959 NE Pacific Street, Box 356-485, Seattle, WA 98195-6485, USA. fanfan@u.washington.edu
Y Imanishi
D A Saperstein
K Palczewski
University of Washington · US

Funding

REGULATION OF RHODOPSIN KINASE AND GUANYLATE CYCLASER01EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF · 1994 to 2014
$9.5M
RETINA SPECIFIC GENE THERAPY WITH MODIFIED LIPOSOMESK11EY000347 · NEI · UNIVERSITY OF WASHINGTON · PI SAPERSTEIN, DAVID A · 1995 to 1999
–
RHODOPSIN KINASE: REGULATION, FUNCTION AND STRUCTURER29EY008061 · NEI · UNIVERSITY OF WASHINGTON · PI PALCZEWSKI, KRZYSZTOF NMI · 1989 to 1993
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NEI NIH HHS EY-00347NEI NIH HHS EY-08061NEI NIH HHS R01 EY008061
6 · The paper itself

Abstract

purposeTo determine the efficiency of baculoviruses (BVs) to transfer recombinant genes in vivo into murine ocular tissues.

methodsRecombinant (r)BVs carrying fluorescent protein (FP) cDNA under the control of cytomegalovirus (CMV) immediate early promoter were constructed. Initially, cultured HEK293 and ARPE19 cells were infected with these rBVs and analyzed for efficiency and stability of transgene expression. The rBV-CMV green (G)FP was also injected into the intravitreal and subretinal space of mouse eye. Mice were periodically analyzed to determine the efficiency and stability of expression by histologic examination under fluorescence microscopy. The effect of rBV-CMV-GFP on the physiology of the retina was analyzed by electroretinography.

resultscDNAs encoding fluorescent proteins were efficiently transduced in HEK293 and ARPE19 cells in vitro. GFP expression in vivo was observed exclusively in retinal pigment epithelial (RPE) cells after subretinal injections. Intravitreal injections of rBV resulted in GFP expression in the corneal endothelium, lens, RPE, and retina. GFP expression was observed for up to 14 days after injection. The infiltration of macrophages, observed 2 days after injection in the area of GFP transduction, had dissipated by day 8 after injection. No alteration in ERG responses was observed 6 weeks after injection of rBV-CMV-GFP.

conclusionsBV efficiently transduces cultured RPE cells and many cell types in vivo in the eye, including endothelial, epithelial, and neuronal cells. BV may be a useful vector for transferring genes in cultured cells and in vivo into ocular tissue.

Indexed as

Genetic VectorsGene Transfer TechniquesOcular Physiological PhenomenaAnimalsBaculoviridaeCell LineElectroretinographyHumansInjectionsMiceMice, Inbred C57BLRecombination, GeneticRetinaRetinitisVitreous Body

Identifiers

PMID11726636
PMCPMC1436034
OpenAlexW2145028780

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.