Article

Three-dimensional tubule formation assay as therapeutic screening model for ocular microvascular disorders

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Abstract

Purpose

This study is aimed to adapt a three-dimensional (3-D) in vitro angiogenesis model to the ophthalmology field using retinal endothelial cells (REC). This system is applied to assess the angiogenic capacity of aqueous humor (AH) from patients with ocular disorders, and to test the effect of VEGF inhibitor (aflibercept) on induced angiogenesis.

Methods

Human REC and umbilical vein endothelial cells (HUVEC) and pericytes were co-cultured in a gel matrix with 25–200 ng/ml pro-angiogenic growth factors (GF). AH from patients with cataract, glaucoma or proliferative diabetic retinopathy (PDR) was tested in the REC-pericyte co-culture. Aflibercept was then introduced to the co-culture containing PDR AH. The surface area and total tubule length were measured using Image J.

Results

Optimal GF concentrations at 200 ng/ml induced angiogenesis by REC as well as HUVEC, while vessel formation by both cell types was strongly reduced using 25–50 ng/ml GF. Addition of AH from the PDR patient triggered tubule formation by REC at low GF concentration. Aflibercept, however, significantly inhibited angiogenesis induced by PDR AH, but showed no significant influence on other conditions.

Conclusion

REC can be applied efficiently in the 3-D in vitro angiogenesis model as a diagnostic tool to assess the AH angiogenic status and to validate new anti-angiogenic therapeutic compounds prior to clinical trial.

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Acknowledgements

We thank Dr. O. G. de Jong for donating the lentiviral GFP and dsRED constructs. Research for this manuscript was (in part) performed within the framework of the Erasmus post-graduate school Molecular Medicine and supported by Uitzicht grant (Uitzicht 2015-10).

Author information

Author notes

  1. These authors contributed equally: Pieter J. M. Leenen, Willem A. Dik.

Affiliations

  1. Department of Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands

    • Mahnaz Shariatzadeh
    •  & Pieter J. M. Leenen
  2. Division of Experimental Cardiology, Department of Cardiology, Thoraxcenter, Erasmus University Medical Center, Rotterdam, The Netherlands

    • Maarten M. Brandt
    •  & Caroline Cheng
  3. Department of Nephrology and Hypertension, DIGD, University Medical Center Utrecht, Utrecht, The Netherlands

    • Caroline Cheng
  4. Department of Ophthalmology, Erasmus University Medical Center, Rotterdam, The Netherlands

    • Josianne C. ten Berge
    •  & Aniki Rothova
  5. Department of Immunology, Laboratory Medical Immunology, Erasmus University Medical Center, Rotterdam, The Netherlands

    • Willem A. Dik

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Conflict of interest

The authors declare that they have no conflict of interest.

Corresponding author

Correspondence to Mahnaz Shariatzadeh.