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Published on: January 19, 2018
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Fluorescent angiogenesis models using gelfoam® implanted in transgenic mice expressing fluorescent proteins
1Department of Surgery, University of California San Diego Medical Center, San Diego, CA, USA.
Methods in Molecular Biology (Clifton, N.J.)
|February 11, 2014
Summary
This study presents an advanced Gelfoam(®) sponge model for in vivo angiogenesis research. This powerful imaging system aids in discovering and evaluating new vascularization agents.
Area of Science:
- * Biomedical Engineering
- * Developmental Biology
- * Cancer Research
Background:
- * Fidler's group previously established an in vivo angiogenesis assay using Gelfoam(®) sponges.
- * Vessels were detected using fluorescent antibodies against CD31.
- * Nestin promoter-driven green fluorescent protein (ND-GFP) mice were utilized.
Purpose of the Study:
- * To develop and validate a novel Gelfoam(®)-based in vivo angiogenesis model.
- * To visualize and quantify angiogenesis and its interactions with cancer cells.
- * To assess blood vessel anastomosis using advanced imaging techniques.
Main Methods:
- * Gelfoam(®) sponges were impregnated with agarose and proangiogenic factors, then implanted in ND-GFP mice.
- * Angiogenesis was quantified by measuring nascent blood vessel length using in vivo fluorescence microscopy.
- * Color-coded imaging models were developed to visualize cancer cell-blood vessel interactions and vessel anastomosis.
Main Results:
- * Gelfoam(®) sponges rapidly vascularized with ND-GFP-expressing nascent blood vessels.
- * A network of nascent blood vessels formed on basic fibroblast growth factor (bFGF)-treated Gelfoam(®).
- * Color-coded imaging successfully visualized interactions between osteosarcoma cells and blood vessels, and blood vessel anastomosis.
Conclusions:
- * The Gelfoam(®) in vivo angiogenesis model is effective for studying vascularization.
- * Fluorescent protein labeling enhances visualization of angiogenesis and related processes.
- * This model serves as a powerful tool for discovering and evaluating agents that influence vascularization.

