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  3. Zebrafish Caudal Fin Angiogenesis Assay-Advanced Quantitative Assessment Including 3-Way Correlative Microscopy.
 

Zebrafish Caudal Fin Angiogenesis Assay-Advanced Quantitative Assessment Including 3-Way Correlative Microscopy.

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BORIS DOI
10.7892/boris.82614
Date of Publication
2016
Publication Type
Article
Division/Institute

Institut für Anatomie...

Author
Hlushchuk, Ruslan
Institut für Anatomie
Brönnimann, Daniel
Institut für Anatomie
Correa Shokiche, Carlos
Institut für Anatomie
Schaad, Laura
Institut für Anatomie
Triet, Ramona
Institut für Anatomie
Jazwinska, Anna
Tschanz, Stefan A.
Institut für Anatomie
Djonov, Valentin Georgiev
Institut für Anatomie
Subject(s)

600 - Technology::610...

Series
PLoS ONE
ISSN or ISBN (if monograph)
1932-6203
Publisher
Public Library of Science
Language
English
Publisher DOI
10.1371/journal.pone.0149281
PubMed ID
26950851
Description
BACKGROUND

Researchers evaluating angiomodulating compounds as a part of scientific projects or pre-clinical studies are often confronted with limitations of applied animal models. The rough and insufficient early-stage compound assessment without reliable quantification of the vascular response counts, at least partially, to the low transition rate to clinics.

OBJECTIVE

To establish an advanced, rapid and cost-effective angiogenesis assay for the precise and sensitive assessment of angiomodulating compounds using zebrafish caudal fin regeneration. It should provide information regarding the angiogenic mechanisms involved and should include qualitative and quantitative data of drug effects in a non-biased and time-efficient way.

APPROACH & RESULTS

Basic vascular parameters (total regenerated area, vascular projection area, contour length, vessel area density) were extracted from in vivo fluorescence microscopy images using a stereological approach. Skeletonization of the vasculature by our custom-made software Skelios provided additional parameters including "graph energy" and "distance to farthest node". The latter gave important insights into the complexity, connectivity and maturation status of the regenerating vascular network. The employment of a reference point (vascular parameters prior amputation) is unique for the model and crucial for a proper assessment. Additionally, the assay provides exceptional possibilities for correlative microscopy by combining in vivo-imaging and morphological investigation of the area of interest. The 3-way correlative microscopy links the dynamic changes in vivo with their structural substrate at the subcellular level.

CONCLUSIONS

The improved zebrafish fin regeneration model with advanced quantitative analysis and optional 3-way correlative morphology is a promising in vivo angiogenesis assay, well-suitable for basic research and preclinical investigations.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/142250
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