Evidence map›Paper›PMID 28143742›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2017

Cone Genesis Tracing by the Chrnb4-EGFP Mouse Line: Evidences of Cellular Material Fusion after Cone Precursor Transplantation.

Sarah Decembrini, Catherine Martin, Florian Sennlaub, Sylvain Chemtob, Martin Biel, Marijana Samardzija, Alexandre Moulin, Francine Behar-Cohen, Yvan Arsenijevic

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

50 citing papers in PubMed, 82 citations in OpenAlex.

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  14. Re-formation of synaptic connectivity in dissociated human stem cell-derived retinal organoid cultures.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

9 authors at 6 institutions in 4 countries.

Sarah DecembriniUnit of Retinal Degeneration and Regeneration, Department of Ophthalmology, University of Lausanne, Hôpital ophtalmique Jules-Gonin, Fondation asile des aveugles, 1004 Lausanne, Switzerland.
Catherine MartinUnit of Retinal Degeneration and Regeneration, Department of Ophthalmology, University of Lausanne, Hôpital ophtalmique Jules-Gonin, Fondation asile des aveugles, 1004 Lausanne, Switzerland.
Florian SennlaubSorbonne Universités, UPMC/Univ Paris 06, UMRS 968, INSERM, U968, Institut de la Vision, 75012 Paris, France.
Sylvain ChemtobDepartments of Pediatrics, Ophthalmology and Pharmacology, Hôpital Ste. Justine Research Center, Montreal, QC H3T1C5, Canada.
Martin BielCenter for Integrated Protein Science Munich CIPSM, Department of Pharmacy-Center for Drug Research, Ludwig-Maximilians-Universität München, 81377 München, Germany.
Marijana SamardzijaLaboratory for Retinal Cell Biology, Department of Ophthalmology, University of Zurich, 8952 Schlieren, Switzerland.
Alexandre MoulinPathology Laboratory, Department of Ophthalmology, University of Lausanne, Hôpital ophtalmique Jules-Gonin, Fondation asile des aveugles, 1004 Lausanne, Switzerland.
Francine Behar-CohenDepartment of Ophthalmology, University of Lausanne, Hôpital ophtalmique Jules-Gonin, Fondation asile des aveugles, 1004 Lausanne, Switzerland.
Yvan ArsenijevicUnit of Retinal Degeneration and Regeneration, Department of Ophthalmology, University of Lausanne, Hôpital ophtalmique Jules-Gonin, Fondation asile des aveugles, 1004 Lausanne, Switzerland. Electronic address: yvan.arsenijevic@fa2.ch.
Fondation Asile des Aveugles · CHUniversity of Lausanne · CHCentre Hospitalier Universitaire Sainte-Justine · CAInserm · FRLudwig-Maximilians-Universität München · DEUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cone function is essential to mediate high visual acuity, color vision, and daylight vision. Inherited cone dystrophies and age-related macular degeneration affect a substantial percentage of the world population. To identify and isolate the most competent cells for transplantation and integration into the retina, cone tracing during development would be an important added value. To that aim, the Chrnb4-EGFP mouse line was characterized throughout retinogenesis. It revealed a sub-population of early retinal progenitors expressing the reporter gene that is progressively restricted to mature cones during retina development. The presence of the native CHRNB4 protein was confirmed in EGFP-positive cells, and it presents a similar pattern in the human retina. Sub-retinal transplantations of distinct subpopulations of Chrnb4-EGFP-expressing cells revealed the embryonic day 15.5 high-EGFP population the most efficient cells to interact with host retinas to provoke the appearance of EGFP-positive cones in the photoreceptor layer. Importantly, transplantations into the DsRed retinas revealed material exchanges between donor and host retinas, as >80% of transplanted EGFP-positive cones also were DsRed positive. Whether this cell material fusion is of significant therapeutic advantage requires further thorough investigations. The Chrnb4-EGFP mouse line definitely opens new research perspectives in cone genesis and retina repair.

Indexed as

Gene ExpressionGenes, ReporterAnimalsCell TrackingGreen Fluorescent ProteinsHumansMacular DegenerationMiceNerve Tissue ProteinsOtx Transcription FactorsReceptors, NicotinicRecombinant Fusion ProteinsRetinaRetinal Cone Photoreceptor CellsRetinoid X Receptor gammaStem CellsChrnb4 protein, mouseenhanced green fluorescent proteinGreen Fluorescent ProteinsNerve Tissue ProteinsOtx2 protein, mouseOtx Transcription FactorsReceptors, NicotinicRecombinant Fusion ProteinsRetinoid X Receptor gammaconesfusionneurodegenerationretinaretinal dystrophytransplantation

Identifiers

PMID28143742
PMCPMC5363218
OpenAlexW2581692952

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.