Evidence map›Paper›PMID 27186070›Full record

ArticleMolecular vision2016

Tenascin-C promotes angiogenesis in fibrovascular membranes in eyes with proliferative diabetic retinopathy.

Yoshiyuki Kobayashi, Shigeo Yoshida, Yedi Zhou, Takahito Nakama, Keijiro Ishikawa, Mitsuru Arima, Shintaro Nakao, Yukio Sassa, Atsunobu Takeda, Toshio Hisatomi and 4 more

Abstract read
In one paragraph

Article in Molecular vision, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Damage-Associated Molecular Patterns (DAMPs) in Retinal Disorders.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Anti-integrin therapy for retinovascular diseases.Expert opinion on investigational drugs · 2020
    Review
  12. Article
  13. Article
  14. Increased expression of periostin and tenascin-C in eyes with neovascular glaucoma secondary to PDR.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2020
    Article
  15. Article
  16. Article
  17. New Therapies of Neovascular AMD-Beyond Anti-VEGFs.Vision (Basel, Switzerland) · 2018
    Review
  18. Periostin in vitreoretinal diseases.Cellular and molecular life sciences : CMLS · 2017
    Review
  19. Article
  20. Tenascins in Retinal and Optic Nerve Neurodegeneration.Frontiers in integrative neuroscience · 2017
    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

14 authors.

Yoshiyuki KobayashiDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Shigeo YoshidaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Yedi ZhouDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Takahito NakamaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Keijiro IshikawaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Mitsuru ArimaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Shintaro NakaoDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Yukio SassaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Atsunobu TakedaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Toshio HisatomiDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Yasuhiro IkedaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Akira MatsudaDepartment of Ophthalmology, Juntendo University, Tokyo, Japan.
Koh-Hei SonodaDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Tatsuro IshibashiDepartment of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe previously demonstrated that tenascin-C was highly expressed in the fibrovascular membranes (FVMs) of patients with proliferative diabetic retinopathy (PDR). However, its role in the pathogenesis of FVMs has not been determined. The purpose of this study was to investigate what role tenascin-C plays in the formation and angiogenesis of FVMs.

methodsThe level of tenascin-C was determined by sandwich enzyme-linked immunosorbent assay in the vitreous samples collected from patients with PDR and with a macular hole as control. The locations of tenascin-C, α- smooth muscle actin (SMA), CD34, glial fibrillary acidic protein (GFAP), and integrin αV in the FVMs from PDR patients were determined by immunohistochemistry. We also measured the in vitro expression of the mRNA and protein of tenascin-C in vascular smooth muscle cells (VSMCs) stimulated by interleukin (IL)-13. The effects of tenascin-C on cell proliferation, migration, and tube formation were determined in human retinal endothelial cells (HRECs) in culture.

resultsThe mean vitreous levels of tenascin-C were significantly higher in patients with PDR than in patients with a macular hole (p<0.001). Double immunofluorescence analyses of FVMs from PDR patients showed that tenascin-C co-stained FVMs with α-SMA, CD34, and integrin αV but not with GFAP. In addition, IL-13 treatment increased both the expression and secretion of tenascin-C by VSMCs in a dose-dependent manner. Tenascin-C exposure promoted proliferation, migration, and tube formation in HRECs. Tenascin-C neutralizing antibody significantly blocked the tube formation by HRECs exposed to VSMC-IL-13-conditioned medium.

conclusionsOur findings suggest that tenascin-C is secreted from VSMCs and promotes angiogenesis in the FVMs associated with PDR.

Indexed as

ActinsAgedAntigens, CD34Cell MovementCell ProliferationCells, CulturedDiabetic RetinopathyEndothelium, VascularEnzyme-Linked Immunosorbent AssayEpiretinal MembraneFemaleFluorescent Antibody Technique, IndirectGlial Fibrillary Acidic ProteinHumansMaleMiddle AgedACTA2 protein, humanActinsAntigens, CD34Glial Fibrillary Acidic ProteinRNA, MessengerTenascin

Identifiers

PMID27186070
PMCPMC4859161

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LicenceCC BY-NC-ND
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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.