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Updated: Jul 17, 2025

Author Spotlight: Advances in Quantifying Microvascular Density in Aging Murine Lungs
Published on: January 3, 2025
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.
Abstract:
Pulmonary vascular dysfunction is characterized by remodeling and loss of microvessels in the lung and is a major manifestation of chronic lung diseases (CLD). In murine models of CLD, the small arterioles and capillaries are the first and most prevalent vessels that are affected by pruning and remodeling. Thus, visualization of the pulmonary arterial vasculature in three dimensions is essential to define pruning and remodeling both temporally and spatially and its role in the pathogenesis of CLD, aging, and tissue repair. To this end, we have developed a novel method to visualize and quantitate the murine pulmonary arterial circulation using microcomputed tomography (µCT) imaging. Using this perfusion technique, we can quantitate microvessels to approximately 6 µM in diameter. We hypothesize that bleomycin-induced injury would have a significant impact on the arterial vascular structure. As proof of principle, we demonstrated that as a result of bleomycin-induced injury at peak fibrosis, significant alterations in arterial vessel structure were visible in the three-dimensional models as well as quantification. Thus, we have successfully developed a perfusion methodology and complementary analysis techniques, which allows for the reconstruction, visualization, and quantitation of the mouse pulmonary arterial microvasculature in three-dimensions. This tool will further support the examination and understanding of angiogenesis during the development of CLD as well as repair following injury.
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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