Evidence map›Paper›PMID 25918849›Full record

ArticlePloS one2015

Characterization of tissue-engineered posterior corneas using second- and third-harmonic generation microscopy.

Louis Jay, Jean-Michel Bourget, Benjamin Goyer, Kanwarpal Singh, Isabelle Brunette, Tsuneyuki Ozaki, Stéphanie Proulx

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Scleral structure and biomechanics.Progress in retinal and eye research · 2020
    Review
  4. Article
  5. Collagen Type I: A Versatile Biomaterial.Advances in experimental medicine and biology
    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.

Louis JayCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, Varennes, Quebec, Canada; Centre de recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada and Département d'ophtalmologie, Université de Montréal, Montréal, Quebec, Canada.
Jean-Michel BourgetCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada and Département d'ophtalmologie, Université de Montréal, Montréal, Quebec, Canada.
Benjamin GoyerAxe médecine régénératrice, Hôpital du Saint-Sacrement, Centre de recherche du CHU de Québec, Québec, Quebec, Canada and Centre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Québec, Quebec, Canada.
Kanwarpal SinghCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, Varennes, Quebec, Canada; Centre de recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada and Département d'ophtalmologie, Université de Montréal, Montréal, Quebec, Canada.
Isabelle BrunetteCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada and Département d'ophtalmologie, Université de Montréal, Montréal, Quebec, Canada.
Tsuneyuki OzakiCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, Varennes, Quebec, Canada.
Stéphanie ProulxAxe médecine régénératrice, Hôpital du Saint-Sacrement, Centre de recherche du CHU de Québec, Québec, Quebec, Canada and Centre de recherche en organogénèse expérimentale de l'Université Laval / LOEX, Québec, Quebec, Canada; Département d'ophtalmologie et d'oto-rhino-laryngologie, Faculté de médecine, Université Laval, Québec, Quebec, Canada.

Funding

Canadian Institutes of Health Research CPG-121034
6 · The paper itself

Abstract

Three-dimensional tissues, such as the cornea, are now being engineered as substitutes for the rehabilitation of vision in patients with blinding corneal diseases. Engineering of tissues for translational purposes requires a non-invasive monitoring to control the quality of the resulting biomaterial. Unfortunately, most current methods still imply invasive steps, such as fixation and staining, to clearly observe the tissue-engineered cornea, a transparent tissue with weak natural contrast. Second- and third-harmonic generation imaging are well known to provide high-contrast, high spatial resolution images of such tissues, by taking advantage of the endogenous contrast agents of the tissue itself. In this article, we imaged tissue-engineered corneal substitutes using both harmonic microscopy and classic histopathology techniques. We demonstrate that second- and third-harmonic imaging can non-invasively provide important information regarding the quality and the integrity of these partial-thickness posterior corneal substitutes (observation of collagen network, fibroblasts and endothelial cells). These two nonlinear imaging modalities offer the new opportunity of monitoring the engineered corneas during the entire process of production.

Indexed as

AdultCollagenCorneaCorneal StromaEndothelial CellsEndothelium, CornealExtracellular MatrixHumansInfantInfant, NewbornMicroscopyTissue EngineeringCollagen

Identifiers

PMID25918849
PMCPMC4412819

What OpenQuestion holds

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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.