Microcomputed tomography visualization and quantitation of the pulmonary arterial microvascular tree in mouse models

Ben Schneider1, Katrina W Kopf2, Emma Mason1

  • 1Department of Medicine, Division of Pulmonary, Critical Care & Sleep Medicine National Jewish Health Denver Colorado USA.

Pulmonary Circulation
|August 30, 2023
PubMed

Insights

Researchers developed a new 3D imaging method to visualize pulmonary arterial microvasculature. This technique quantifies changes in blood vessels, aiding the study of lung diseases and repair.

Area of Science:

  • Pulmonary vascular biology
  • Medical imaging
  • Fibrotic lung disease research

Background:

  • Pulmonary vascular dysfunction, marked by microvessel loss, is key in chronic lung diseases (CLD).
  • Small pulmonary arterioles and capillaries are initially affected by pruning and remodeling in CLD models.
  • 3D visualization is crucial for understanding vascular changes in CLD, aging, and tissue repair.

Purpose of the Study:

  • To develop a novel method for 3D visualization and quantification of the murine pulmonary arterial circulation.
  • To assess the impact of bleomycin-induced injury on pulmonary arterial vascular structure.

Main Methods:

  • Development of a novel perfusion-based microcomputed tomography (µCT) imaging technique.
  • Quantification of microvessels down to approximately 6 µM in diameter.
  • 3D reconstruction and analysis of pulmonary arterial vasculature.

Main Results:

  • Successful development of a perfusion methodology for 3D visualization and quantification of mouse pulmonary microvasculature.
  • Demonstration of significant alterations in arterial vessel structure following bleomycin-induced injury and peak fibrosis.
  • Validation of the technique's ability to visualize and quantitate microvascular changes.

Conclusions:

  • A novel 3D perfusion µCT method enables detailed visualization and quantification of pulmonary arterial microvasculature.
  • This technique effectively captures structural changes in pulmonary vasculature following fibrotic injury.
  • The developed tool will advance the study of angiogenesis in CLD development and tissue repair.

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