RGD targeting of human ferritin iron oxide nanoparticles enhances in vivo MRI of vascular inflammation and angiogenesis in experimental carotid disease and abdominal aortic aneurysm

J Magn Reson Imaging. 2017 Apr;45(4):1144-1153. doi: 10.1002/jmri.25459. Epub 2016 Sep 30.

Abstract

Purpose: To evaluate Arg-Gly-Asp (RGD)-conjugated human ferritin (HFn) iron oxide nanoparticles for in vivo magnetic resonance imaging (MRI) of vascular inflammation and angiogenesis in experimental carotid disease and abdominal aortic aneurysm (AAA).

Materials and methods: HFn was genetically engineered to express the RGD peptide and Fe3 O4 nanoparticles were chemically synthesized inside the engineered HFn (RGD-HFn). Macrophage-rich left carotid lesions were induced by ligation in FVB mice made hyperlipidemic and diabetic (n = 14), with the contralateral right carotid serving as control. Murine AAAs were created by continuous angiotensin II infusion in ApoE-deficient mice (n = 12), while control mice underwent saline infusion (n = 8). All mice were imaged before and after intravenous injection with either RGD-HFn-Fe3 O4 or HFn-Fe3 O4 using a gradient-echo sequence on a whole-body 3T clinical scanner, followed by histological analysis. The nanoparticle accumulation was assessed by the extent of T2*-induced carotid lumen reduction (% lumen loss) or aortic T2*-weighted signal intensity reduction (% SI [signal intensity] loss).

Results: RGD-HFn-Fe3 O4 was taken up more than HFn-Fe3 O4 in both the ligated left carotid arteries (% lumen loss; 69 ± 9% vs. 36 ± 7%, P = 0.01) and AAAs (% SI loss; 47 ± 6% vs. 20 ± 5%, P = 0.01). The AAA % SI loss correlated positively with AAA size (r = 0.89, P < 0.001). Histology confirmed the greater accumulation and colocalization of RGD-HFn-Fe3 O4 to both vascular macrophages and endothelial cells.

Conclusion: RGD-HFn-Fe3 O4 enhances in vivo MRI by targeting both vascular inflammation and angiogenesis, and provides a promising translatable MRI approach to detect high-risk atherosclerotic and aneurysmal vascular diseases.

Level of evidence: 1 J. Magn. Reson. Imaging 2017;45:1144-1153.

Keywords: RGD; aneurysms; angiogenesis; atherosclerosis; iron; nanoparticles.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aortic Aneurysm, Abdominal / diagnostic imaging
  • Aortic Aneurysm, Abdominal / metabolism
  • Aortic Aneurysm, Abdominal / physiopathology*
  • Carotid Arteries / diagnostic imaging
  • Carotid Arteries / metabolism
  • Carotid Arteries / physiopathology
  • Carotid Artery Diseases / diagnostic imaging
  • Carotid Artery Diseases / metabolism
  • Carotid Artery Diseases / physiopathology*
  • Disease Models, Animal
  • Ferric Compounds / metabolism
  • Ferritins / metabolism*
  • Inflammation / diagnostic imaging
  • Inflammation / metabolism
  • Inflammation / physiopathology*
  • Magnetic Resonance Imaging / methods*
  • Male
  • Mice
  • Nanoparticles
  • Neovascularization, Pathologic / diagnostic imaging
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / physiopathology
  • Oligopeptides / metabolism*
  • Vascular Diseases / diagnostic imaging
  • Vascular Diseases / metabolism
  • Vascular Diseases / physiopathology

Substances

  • Ferric Compounds
  • Oligopeptides
  • ferric oxide
  • arginyl-glycyl-aspartic acid
  • Ferritins