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Updated: Jul 7, 2026

An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis
Published on: August 6, 2020
SDF1-alpha is associated with VEGFR-2 in human choroidal neovascularisation
Eoin Guerin1, Carl Sheridan, David Assheton
1Unit of Ophthalmology, Department of Clinical Sciences, UCD, Duncan Building, University of Liverpool, Daulby Street, Liverpool, L69 3GA, United Kingdom. eoinguerin@gmail.com
Stromal cell derived factor 1-alpha (SDF) and its receptor CXCR4 may play a role in choroidal neovascularisation (CNV). SDF, potentially produced by the retinal pigment epithelium (RPE), was detected in various CNV specimens, suggesting its involvement in neovascularization.
Area of Science:
- Ophthalmology
- Cell Biology
- Immunology
Background:
- Endothelial progenitor cells (EPCs) are implicated in choroidal neovascularisation (CNV).
- EPC recruitment relies on stromal cell derived factor 1-alpha (SDF) and its receptor CXCR4.
Purpose of the Study:
- To investigate the presence and distribution of SDF and CXCR4 in human CNV specimens.
- To determine the potential role of the SDF/CXCR4 pathway in neovascularisation.
Main Methods:
- Immunohistochemistry was performed on 23 CNV specimens from various aetiologies.
- Antibodies used included SDF, CXCR4, VEGFR-2, CD34, CD68, and cytokeratins.
Main Results:
- SDF was detected in multiple CNV specimens, with significant association with VEGFR-2 and RPE localisation.
- CXCR4 immunostaining was widespread across all specimens.
- A significant association was found between SDF and VEGFR-2 immunostaining (p<0.001) and SDF localisation to the RPE (p<0.05).
Conclusions:
- SDF, potentially produced by the RPE, may contribute to the pathogenesis of CNV.
- The SDF/CXCR4 pathway is a potential target for therapeutic interventions in CNV.
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