ArticlePLoS computational biology2012
Adhesion failures determine the pattern of choroidal neovascularization in the eye: a computer simulation study.
Article in PLoS computational biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed.
- Improving 3D deep learning segmentation with biophysically motivated cell synthesis.Communications biology · 2025Article
- A computational dynamic systems model forCurrent research in toxicology · 2025Article
- RNA-seq analysis of ageing human retinal pigment epithelium: Unexpected up-regulation of visual cycle gene transcription.Journal of cellular and molecular medicine · 2021Article
- A Baseline Score to Predict Response to Ranibizumab Treatment in Neovascular Age-Related Macular Degeneration.Translational vision science & technology · 2021Article
- Anomalous Angiogenesis in Retina.Biomedicines · 2021Article
- Altered Protein Function Caused by AMD-associated Variant rs704 Links Vitronectin to Disease Pathology.Investigative ophthalmology & visual science · 2020Article
- HtrA1 Mediated Intracellular Effects on Tubulin Using a Polarized RPE Disease Model.EBioMedicine · 2018Article
- An in silico model of retinal cholesterol dynamics (RCD model): insights into the pathophysiology of dry AMD.Journal of lipid research · 2017Article
- Progression of Diabetic Capillary Occlusion: A Model.PLoS computational biology · 2016Article
- Article
- RPE Cell and Sheet Properties in Normal and Diseased Eyes.Advances in experimental medicine and biology · 2016Article
- Computational Screening of Tip and Stalk Cell Behavior Proposes a Role for Apelin Signaling in Sprout Progression.PloS one · 2016Article
- Aflibercept: a review of its use in the treatment of choroidal neovascularization due to age-related macular degeneration.Clinical ophthalmology (Auckland, N.Z.) · 2015Review
- Article
- Collective cell streams in epithelial monolayers depend on cell adhesion.New journal of physics · 2013Article
- Mathematical modeling approaches in the study of glaucoma disparities among people of African and European descents.Journal of coupled systems and multiscale dynamics · 2013Article
- Cellular potts modeling of tumor growth, tumor invasion, and tumor evolution.Frontiers in oncology · 2013Article
- Cell-based multi-parametric model of cleft progression during submandibular salivary gland branching morphogenesis.PLoS computational biology · 2013Article
- Rap1 GTPase activation and barrier enhancement in rpe inhibits choroidal neovascularization in vivo.PloS one · 2013Article
- Ocular hemodynamics and glaucoma: the role of mathematical modeling.European journal of ophthalmologyReview
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Authors and funding
7 authors.
Funding
Abstract
Choroidal neovascularization (CNV) of the macular area of the retina is the major cause of severe vision loss in adults. In CNV, after choriocapillaries initially penetrate Bruch's membrane (BrM), invading vessels may regress or expand (CNV initiation). Next, during Early and Late CNV, the expanding vasculature usually spreads in one of three distinct patterns: in a layer between BrM and the retinal pigment epithelium (sub-RPE or Type 1 CNV), in a layer between the RPE and the photoreceptors (sub-retinal or Type 2 CNV) or in both loci simultaneously (combined pattern or Type 3 CNV). While most studies hypothesize that CNV primarily results from growth-factor effects or holes in BrM, our three-dimensional simulations of multi-cell model of the normal and pathological maculae recapitulate the three growth patterns, under the hypothesis that CNV results from combinations of impairment of: 1) RPE-RPE epithelial junctional adhesion, 2) Adhesion of the RPE basement membrane complex to BrM (RPE-BrM adhesion), and 3) Adhesion of the RPE to the photoreceptor outer segments (RPE-POS adhesion). Our key findings are that when an endothelial tip cell penetrates BrM: 1) RPE with normal epithelial junctions, basal attachment to BrM and apical attachment to POS resists CNV. 2) Small holes in BrM do not, by themselves, initiate CNV. 3) RPE with normal epithelial junctions and normal apical RPE-POS adhesion, but weak adhesion to BrM (e.g. due to lipid accumulation in BrM) results in Early sub-RPE CNV. 4) Normal adhesion of RBaM to BrM, but reduced apical RPE-POS or epithelial RPE-RPE adhesion (e.g. due to inflammation) results in Early sub-retinal CNV. 5) Simultaneous reduction in RPE-RPE epithelial binding and RPE-BrM adhesion results in either sub-RPE or sub-retinal CNV which often progresses to combined pattern CNV. These findings suggest that defects in adhesion dominate CNV initiation and progression.
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