Semi-automated protocol to quantify and characterize fluorescent three-dimensional vascular images

PLoS One. 2024 May 16;19(5):e0289109. doi: 10.1371/journal.pone.0289109. eCollection 2024.

Abstract

The microvasculature facilitates gas exchange, provides nutrients to cells, and regulates blood flow in response to stimuli. Vascular abnormalities are an indicator of pathology for various conditions, such as compromised vessel integrity in small vessel disease and angiogenesis in tumors. Traditional immunohistochemistry enables the visualization of tissue cross-sections containing exogenously labeled vasculature. Although this approach can be utilized to quantify vascular changes within small fields of view, it is not a practical way to study the vasculature on the scale of whole organs. Three-dimensional (3D) imaging presents a more appropriate method to visualize the vascular architecture in tissue. Here we describe the complete protocol that we use to characterize the vasculature of different organs in mice encompassing the methods to fluorescently label vessels, optically clear tissue, collect 3D vascular images, and quantify these vascular images with a semi-automated approach. To validate the automated segmentation of vascular images, one user manually segmented one hundred random regions of interest across different vascular images. The automated segmentation results had an average sensitivity of 83±11% and an average specificity of 91±6% when compared to manual segmentation. Applying this procedure of image analysis presents a method to reliably quantify and characterize vascular networks in a timely fashion. This procedure is also applicable to other methods of tissue clearing and vascular labels that generate 3D images of microvasculature.

MeSH terms

  • Animals
  • Automation
  • Imaging, Three-Dimensional* / methods
  • Mice
  • Microvessels / diagnostic imaging

Grants and funding

This work was supported in part by the National Institutes of Health (R21AG066000 to DX and BC, 5TL1TR001415-07 to CC, R21NS111984 to DC, MF, and BC, R01NS020989 to DC, MF, and BC, P41EB015890 to BC, http://www.nih.gov/) and the Arnold and Mabel Beckman Foundation (http://www.beckman-foundation.org/) to BC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.