Multimodal Study of Murine Cardiovascular Remodeling: Four-Dimensional Ultrasound and Mass Spectrometry Imaging

Amelya G Fox1, Kelsey E Buonodono1, Allison R Jones1

  • 1Mechanical, Aerospace, and Biomedical Engineering, University of Tennessee.

Insights

This study introduces a new method combining 4D ultrasound and mass spectrometry imaging to analyze cardiovascular disease in mice. This approach offers detailed insights into cardiac function and molecular changes for better disease understanding.

Area of Science:

  • Cardiovascular Science
  • Biomedical Imaging
  • Molecular Pathology

Background:

  • Cardiovascular disease (CVD) is a leading cause of death, involving structural and functional changes in the heart and vasculature.
  • Current detection methods for CVD include ultrasound (US) imaging for organ-level analysis and mass spectrometry imaging (MSI) for molecular-level insights.
  • Existing techniques lack a combined approach to simultaneously assess cardiovascular hemodynamics, biomechanics, and molecular composition.

Purpose of the Study:

  • To present an innovative methodology for studying murine cardiac pathophysiology.
  • To couple in vivo four-dimensional (4D) ultrasound imaging with ex vivo matrix-assisted laser desorption/ionization (MALDI) MSI of the heart.
  • To enable comprehensive analysis of cardiovascular structure, function, and molecular changes in disease models.

Main Methods:

  • Utilizing 4D ultrasound to capture dynamic volumetric measurements, including radial displacement and strain throughout the cardiac cycle.
  • Employing MALDI MSI for untargeted lipidomic analysis of cardiac tissue.
  • Integrating US and MSI to assess vessel wall composition, hemodynamics, and biomechanics.

Main Results:

  • The combined 4D ultrasound and MALDI MSI methodology allows for detailed quantification of cardiac function and biomechanics.
  • MSI provides molecular-level insights into tissue composition, identifying specific lipids, metabolites, peptides, and glycans.
  • The integrated approach facilitates the study of structural and functional changes in cardiovascular disease models.

Conclusions:

  • This novel integrated imaging approach provides a powerful tool for investigating cardiovascular pathophysiology in preclinical models.
  • The methodology enables simultaneous assessment of cardiovascular hemodynamics, biomechanics, and molecular profiles.
  • This technique can be adapted to study various cardiovascular diseases by modifying imaging parameters and MSI targets.