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Fractal and Image Analysis of the Microvasculature in Normal Intestinal Submucosa and Intestinal Polyps in Apc Min/+ Mice
Tumors are supported by the development of a unique vascular bed. We used fractal dimension ( Db ) and image analysis to quantify differences in the complexity of the vasculature in normal intestinal submucosa and intestinal polyps. Apc Min/+ mice and wild-type mice were perfused with a curable late...
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Published in: | Microscopy and microanalysis 2010-02, Vol.16 (1), p.73-79 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Tumors are supported by the development of a unique vascular bed. We used fractal dimension (
Db
) and image analysis to quantify differences in the complexity of the vasculature in normal intestinal submucosa and intestinal polyps.
Apc
Min/+
mice and wild-type mice were perfused with a curable latex compound, intestines sectioned, and images collected via confocal microscopy. The images were analyzed and area (A), perimeter (P), and integrated optical density (IOD) of the normal and tumor vascular beds were measured. The
Db
, a quantitative descriptor of morphological complexity, was significantly greater for the polyp vasculature from
Apc
Min/+
mice than controls. This indicates that the polyp microvasculature is more chaotic than that of the controls, while the IOD and average vascular density values displayed no differences. This suggests the mass of blood volume is equivalent in normal and polyp microvasculature. The lower vascular area-perimeter ratios expressed by the polyp microvasculature suggest it is composed of smaller, more tortuous vessels. These data demonstrate that fractal analysis is applicable for providing a quantitative description of vascular complexity associated with angiogenesis occurring in normal or diseased tissue. Application of
Db
, IOD, and average density provides a clearer quantification of the complex morphology associated with tissue microvasculature. |
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ISSN: | 1431-9276 1435-8115 |
DOI: | 10.1017/S143192760999119X |