Evidence map›Paper›PMID 26230410›Full record

ArticlePloS one2015

The Ultrastructural Localization of Type II, IV, and VI Collagens at the Vitreoretinal Interface.

Shao Chong Bu, Roel Kuijer, Roelofje J van der Worp, Xiao Rong Li, Johanna M M Hooymans, Leonoor I Los

Open access · goldAbstract 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Structure and mechanics of the vitreoretinal interface.Journal of the mechanical behavior of biomedical materials · 2022
    Review
  5. Review
  6. Article
  7. Review
  8. 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

6 authors at 3 institutions in 2 countries.

Shao Chong BuDepartment of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; W.J. Kolff Institute, Graduate School of Medical Sciences, University of Groningen, Groningen, the Netherlands; Tianjin Medical University Eye Hospital, Tianjin Medical University, Tianjin, China, Fu Kang Street 251, Nan Kai District, Tianjin, 300384, China.
Roel KuijerDepartment of Biomedical Engineering, FB40, University of Groningen, University Medical Center Groningen, A. Deusinglaan 1, building 3215, FB40, 9713 AV, Groningen, The Netherlands; W.J. Kolff Institute, Graduate School of Medical Sciences, University of Groningen, Groningen, the Netherlands.
Roelofje J van der WorpDepartment of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; W.J. Kolff Institute, Graduate School of Medical Sciences, University of Groningen, Groningen, the Netherlands.
Xiao Rong LiTianjin Medical University Eye Hospital, Tianjin Medical University, Tianjin, China, Fu Kang Street 251, Nan Kai District, Tianjin, 300384, China.
Johanna M M HooymansDepartment of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; W.J. Kolff Institute, Graduate School of Medical Sciences, University of Groningen, Groningen, the Netherlands.
Leonoor I LosDepartment of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; W.J. Kolff Institute, Graduate School of Medical Sciences, University of Groningen, Groningen, the Netherlands.
University Medical Center Groningen · NLUniversity of Groningen · NLTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe vitreoretinal interface is the border of the cortical vitreous and the inner surface of the retina. The adhesion of the cortical vitreous to the ILM, namely vitreoretinal adhesion, involves a series of complex molecular adhesion mechanisms and has been considered as an important pathogenic factor in many vitreoretinal diseases. The presence of type VI collagen at the vitreoretinal interface and its possible interaction with collagens and glycoproteins indicates that type VI collagen may contribute to the vitreoretinal adhesion. PURPOSE: To clarify the ultrastructural location of type VI collagen and its relationship to type II and IV collagens at the vitreoretinal interface.

methodsThe ultrastructural localization of type II, IV and VI collagens in the adult human vitreoretinal interface of five donor eyes was evaluated by transmission electron microscopy using immunogold labeling.

resultsIn the pre-equatorial region, we observed densely packed vitreous lamellae with a partly intraretinal course containing type II and VI collagens, reticular structures containing type IV and VI collagens and a thin inner limiting membrane (ILM) containing type IV and VI collagens in a linear distribution pattern. From the anterior to the posterior retina, the linear pattern of type IV and VI collagen labeling gradually became more diffusely present throughout the entire thickness of the ILM.

conclusionsThe presence of type VI collagen in vitreous lamellae penetrating the ILM into the superficial retina suggests that type VI collagen may be involved in the organization of vitreous fibers into lamellae and in the adhesion of the vitreous fibers to the retina. The close relation of type VI to type IV collagen in the ILM suggests that type VI collagen is an important collagen type in the ILM. The topographic variations of type IV and VI collagens in the different regions of the ILM suggest a regional heterogeneity of the ILM. The reticular labeling pattern of type IV and VI collagens observed in the anterior vitreous are highly similar to labeling patterns of blood vessel walls. In the anterior vitreous, they may represent remnants of the regressed embryonic hyaloid blood vessel system. Their presence is in support of the theory on interactive remodeling of the developing vitreous as opposed to the main stream theory of displacement and compression of the primary by the secondary vitreous.

Indexed as

AgedCollagenHumansMicroscopy, Electron, TransmissionMiddle AgedRetinaVitreous BodyCollagen

Identifiers

PMID26230410
PMCPMC4521792
OpenAlexW935947261

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Registered trials

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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.