Compensatory UTE/T2W imaging of inflammatory vascular wall in hyperlipidemic rabbits

Bongjune Kim, Jaemoon Yang, Young Han Lee, Myeong Hoon Kim, Dan Heo, Eugene Lee, Jin Suck Suh, Seungjoo Haam, Yong Min Huh

Research output: Contribution to journalArticle

Abstract

Objectives To obtain compensatory ultra-short echo time (UTE) imaging and T2-weighted (T2W) imaging of Watanabe heritable hyperlipidemic (WHHL) rabbits following dextran-coated magnetic nanocluster (DMNC) injection for the effective in vivo detection of inflammatory vascular wall. Methods Magnetic nanoparticle was synthesized by thermal decomposition and encapsulated with dextran to prepare DMNC. The contrast enhancement efficiency of DMNC was investigated using UTE (repetition time [TR] = 5.58 and TE = 0.07 ms) and T2W (TR = 4000 and TE = 60 ms) imaging sequences. To confirmthe internalization of DMNC into macrophages, DMNC-treated macrophages were visualized by cellular transmission electron microscope (TEM) andmagnetic resonance (MR) imaging.WHHL rabbits expressing macrophage-rich plaques were subjected to UTE and T2Wimaging before and after intravenous DMNC (120 μmol Fe/kg) treatment. Ex vivo MR imaging of plaques and immunostaining studies were also performed. Results Positive and negative contrast enhancement of DMNC solutions with increasing Fe concentrations were observed in UTE and T2W imaging, respectively. The relative signal intensities of the DMNC solution containing 2.9 mM Fe were calculated as 3.53 and 0.99 in UTE and T2W imaging, respectively. DMNC uptake into the macrophage cytoplasm was visualized by electron microscopy. Cellular MR imaging of DMNC-treated macrophages revealed relative signals of 3.00 in UTE imaging and 0.98 in T2W imaging. In vivo MR images revealed significant brightening and darkening of plaque areas in the WHHL rabbit 24 h after DMNC injection in UTE and T2W imaging, respectively. Ex vivo MR imaging results agreed with these in vivo MR imaging results. Histological analysis showed that DMNCs were localized to areas of inflammatory vascular wall.

Original languageEnglish
Article number0124572
JournalPloS one
Volume10
Issue number5
DOIs
Publication statusPublished - 2015 May 15

Fingerprint

Dextrans
dextran
blood vessels
Nanoclusters
Blood Vessels
rabbits
image analysis
Rabbits
Imaging techniques
Macrophages
macrophages
injection
Injections
thermal degradation
transmission electron microscopes
nanoparticles
Nanoparticles
Electron microscopy
Electron Microscopy
Cytoplasm

All Science Journal Classification (ASJC) codes

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

Kim, Bongjune ; Yang, Jaemoon ; Lee, Young Han ; Kim, Myeong Hoon ; Heo, Dan ; Lee, Eugene ; Suh, Jin Suck ; Haam, Seungjoo ; Huh, Yong Min. / Compensatory UTE/T2W imaging of inflammatory vascular wall in hyperlipidemic rabbits. In: PloS one. 2015 ; Vol. 10, No. 5.
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title = "Compensatory UTE/T2W imaging of inflammatory vascular wall in hyperlipidemic rabbits",
abstract = "Objectives To obtain compensatory ultra-short echo time (UTE) imaging and T2-weighted (T2W) imaging of Watanabe heritable hyperlipidemic (WHHL) rabbits following dextran-coated magnetic nanocluster (DMNC) injection for the effective in vivo detection of inflammatory vascular wall. Methods Magnetic nanoparticle was synthesized by thermal decomposition and encapsulated with dextran to prepare DMNC. The contrast enhancement efficiency of DMNC was investigated using UTE (repetition time [TR] = 5.58 and TE = 0.07 ms) and T2W (TR = 4000 and TE = 60 ms) imaging sequences. To confirmthe internalization of DMNC into macrophages, DMNC-treated macrophages were visualized by cellular transmission electron microscope (TEM) andmagnetic resonance (MR) imaging.WHHL rabbits expressing macrophage-rich plaques were subjected to UTE and T2Wimaging before and after intravenous DMNC (120 μmol Fe/kg) treatment. Ex vivo MR imaging of plaques and immunostaining studies were also performed. Results Positive and negative contrast enhancement of DMNC solutions with increasing Fe concentrations were observed in UTE and T2W imaging, respectively. The relative signal intensities of the DMNC solution containing 2.9 mM Fe were calculated as 3.53 and 0.99 in UTE and T2W imaging, respectively. DMNC uptake into the macrophage cytoplasm was visualized by electron microscopy. Cellular MR imaging of DMNC-treated macrophages revealed relative signals of 3.00 in UTE imaging and 0.98 in T2W imaging. In vivo MR images revealed significant brightening and darkening of plaque areas in the WHHL rabbit 24 h after DMNC injection in UTE and T2W imaging, respectively. Ex vivo MR imaging results agreed with these in vivo MR imaging results. Histological analysis showed that DMNCs were localized to areas of inflammatory vascular wall.",
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Compensatory UTE/T2W imaging of inflammatory vascular wall in hyperlipidemic rabbits. / Kim, Bongjune; Yang, Jaemoon; Lee, Young Han; Kim, Myeong Hoon; Heo, Dan; Lee, Eugene; Suh, Jin Suck; Haam, Seungjoo; Huh, Yong Min.

In: PloS one, Vol. 10, No. 5, 0124572, 15.05.2015.

Research output: Contribution to journalArticle

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AU - Yang, Jaemoon

AU - Lee, Young Han

AU - Kim, Myeong Hoon

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AU - Lee, Eugene

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AU - Haam, Seungjoo

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AB - Objectives To obtain compensatory ultra-short echo time (UTE) imaging and T2-weighted (T2W) imaging of Watanabe heritable hyperlipidemic (WHHL) rabbits following dextran-coated magnetic nanocluster (DMNC) injection for the effective in vivo detection of inflammatory vascular wall. Methods Magnetic nanoparticle was synthesized by thermal decomposition and encapsulated with dextran to prepare DMNC. The contrast enhancement efficiency of DMNC was investigated using UTE (repetition time [TR] = 5.58 and TE = 0.07 ms) and T2W (TR = 4000 and TE = 60 ms) imaging sequences. To confirmthe internalization of DMNC into macrophages, DMNC-treated macrophages were visualized by cellular transmission electron microscope (TEM) andmagnetic resonance (MR) imaging.WHHL rabbits expressing macrophage-rich plaques were subjected to UTE and T2Wimaging before and after intravenous DMNC (120 μmol Fe/kg) treatment. Ex vivo MR imaging of plaques and immunostaining studies were also performed. Results Positive and negative contrast enhancement of DMNC solutions with increasing Fe concentrations were observed in UTE and T2W imaging, respectively. The relative signal intensities of the DMNC solution containing 2.9 mM Fe were calculated as 3.53 and 0.99 in UTE and T2W imaging, respectively. DMNC uptake into the macrophage cytoplasm was visualized by electron microscopy. Cellular MR imaging of DMNC-treated macrophages revealed relative signals of 3.00 in UTE imaging and 0.98 in T2W imaging. In vivo MR images revealed significant brightening and darkening of plaque areas in the WHHL rabbit 24 h after DMNC injection in UTE and T2W imaging, respectively. Ex vivo MR imaging results agreed with these in vivo MR imaging results. Histological analysis showed that DMNCs were localized to areas of inflammatory vascular wall.

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