Detection of Macrophage Localization in the Abdominal Aortic Aneurysm Wall Using Ex Vivo Superparamagnetic Iron

Michihisa Umetsu1, Hitoshi Goto1, Yasuhiro Nakamura2

  • 1Division of Vascular Surgery, Department of Surgery, Tohoku University Hospital, Sendai, Miyagi, Japan.

Abstract

Insights

Superparamagnetic iron oxide (SPIO) enhanced MRI can detect macrophages in the abdominal aortic aneurysm (AAA) wall. This imaging technique shows potential for evaluating AAA pathogenesis by visualizing macrophage localization.

Area of Science:

  • Biomedical Imaging
  • Vascular Biology
  • Immunology

Background:

  • Macrophages are key players in abdominal aortic aneurysm (AAA) pathogenesis.
  • Superparamagnetic iron oxide (SPIO) is a macrophage-specific MRI contrast agent.
  • Previous studies focused on SPIO-enhanced MRI of AAA thrombus, not the vessel wall.

Purpose of the Study:

  • To evaluate macrophage localization in the media and adventitia of the AAA wall using SPIO-enhanced MRI.
  • To investigate the role of macrophages in AAA pathogenesis through detailed wall analysis.

Main Methods:

  • Patients undergoing open AAA surgery were divided into SPIO-injected (n=7) and control groups.
  • Ex vivo MRI of harvested AAA walls was performed on the SPIO group.
  • Histological evaluation using Berlin blue (BB) staining assessed macrophage presence and SPIO uptake.

Main Results:

  • A significantly higher proportion of BB-stained macrophages was observed in the SPIO group compared to controls (0.93 vs. 0.03, P < 0.05).
  • A positive correlation was found between BB-stained macrophage counts and BB-stained areas in the SPIO group (τ = 0.58, P < 0.05).
  • SPIO-enhanced MRI regions of interest correlated significantly with BB-stained areas in the media and adventitia of 5 out of 7 patients.

Conclusions:

  • Macrophages in the AAA wall media and adventitia effectively uptake SPIO contrast agent.
  • Ex vivo MRI successfully detected SPIO-labeled macrophages in the AAA wall.
  • SPIO-enhanced MRI holds potential as a novel imaging biomarker for assessing AAA pathogenesis.