Segmentation-Less, automated, vascular vectorization

• Main Authors: Dunn, A.K (Author), Hassan, A.M (Author), Jones, T.A (Author), Mihelic, S.A (Author), Sikora, W.A (Author), Williamson, M.R (Author)
• Format: Article
• Language: English
• Published: Public Library of Science 2021
• Subjects: algorithm; animal; animal experiment; animal tissue; Animals; arteriole; article; biology; brain; Brain; brain circulation; capillary; Cerebrovascular Circulation; Computational Biology; controlled study; data analysis software; diagnostic imaging; endothelium; extraction; filtration; fluorescence microscopy; human; image processing; Image Processing, Computer-Assisted; image quality; image segmentation; in vivo study; machine learning; male; Mice; Microscopy, Fluorescence; microvasculature; Microvessels; mouse; nonhuman; physiology; procedures; simulation; surface area; vascularization; venule
• Online Access: View Fulltext in Publisher

 Recent advances in two-photon fluorescence microscopy (2PM) have allowed large scale imaging and analysis of blood vessel networks in living mice. However, extracting network graphs and vector representations for the dense capillary bed remains a bottleneck in many applications. Vascular vectorization is algorithmically difficult because blood vessels have many shapes and sizes, the samples are often unevenly illuminated, and large image volumes are required to achieve good statistical power. State-of-the-art, three-dimensional, vascular vectorization approaches often require a segmented (binary) image, relying on manual or supervised-machine annotation. Therefore, voxel-by-voxel image segmentation is biased by the human annotator or trainer. Furthermore, segmented images oftentimes require remedial morphological filtering before skeletonization or vectorization. To address these limitations, we present a vectorization method to extract vascular objects directly from unsegmented images without the need for machine learning or training. The Segmentation-Less, Automated, Vascular Vectorization (SLAVV) source code in MATLAB is openly available on GitHub. This novel method uses simple models of vascular anatomy, efficient linear filtering, and vector extraction algorithms to remove the image segmentation requirement, replacing it with manual or automated vector classification. Semi-automated SLAVV is demonstrated on three in vivo 2PM image volumes of microvascular networks (capillaries, arterioles and venules) in the mouse cortex. Vectorization performance is proven robust to the choice of plasma- or endothelial-labeled contrast, and processing costs are shown to scale with input image volume. Fully-automated SLAVV performance is evaluated on simulated 2PM images of varying quality all based on the large (1.4×0.9×0.6 mm3 and 1.6×108 voxel) input image. Vascular statistics of interest (e.g. volume fraction, surface area density) calculated from automatically vectorized images show greater robustness to image quality than those calculated from intensity-thresholded images. Copyright: © 2021 Mihelic et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.