In vivo real-time vessel imaging and ex vivo 3D reconstruction of atherosclerotic plaque in apolipoprotein E-knockout mice using synchrotron radiation microscopy

Jin Won Kim, Hong Seog Seo, Y. Hwu, Jung Ho Je, Aeree Kim, Chil Hwan Oh, Soon Yong Suh, Seung-Woon Rha, Chang Gyu Park, Dong Joo Oh

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Background: To examine the pathophysiology of atherosclerosis, imaging the vascular wall and pathology without tissue damage is required. We used the unmonochromatized synchrotron X-ray to acquire in vivo real-time and ex vivo images of atherosclerotic lesions in apo E-knockout mice without contrast agents or staining. Methods: In the five apo E-knockout mice (apo E-/-, 12, 24, 32, 48, 62-week-old, 3 males) and age/sex matched five wild type mice on cow diets, we acquired in vivo real-time images of thoracic aorta without contrast agents and then, the central arterial trees were dissected intact. Ex vivo synchrotron images with tomographic reconstruction were done and compared with the corresponding pathology. Results: For all living animals, in vivo real-time images of thoracic aorta could be acquired without contrast agents but could not identify the atherosclerotic lesions. Ex vivo images accurately determined aortic wall and atherosclerotic plaque without staining in comparison to histopathology according to the AHA classification (r = 0.84, p < 0.001). The volume rendered 3 D images of plaque showed central cholesterol clefts as matched with optical images. Conclusions: The combination of synchrotron enhanced X-ray microscopy and genetically engineered hyperlipidemic animals would be a useful tool to investigate the changes of advanced atherosclerotic lesions.

Original languageEnglish
Pages (from-to)166-171
Number of pages6
JournalInternational Journal of Cardiology
Volume114
Issue number2
DOIs
Publication statusPublished - 2007 Jan 8

Fingerprint

Synchrotrons
Apolipoproteins E
Atherosclerotic Plaques
Knockout Mice
Contrast Media
Microscopy
Radiation
Thoracic Aorta
X-Rays
Pathology
Staining and Labeling
Genetically Modified Animals
Three-Dimensional Imaging
Blood Vessels
Atherosclerosis
Cholesterol
Diet

Keywords

  • Apo E-knockout mouse
  • Atherosclerosis
  • Plaque
  • Synchrotron
  • Unmonochromatized

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

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title = "In vivo real-time vessel imaging and ex vivo 3D reconstruction of atherosclerotic plaque in apolipoprotein E-knockout mice using synchrotron radiation microscopy",
abstract = "Background: To examine the pathophysiology of atherosclerosis, imaging the vascular wall and pathology without tissue damage is required. We used the unmonochromatized synchrotron X-ray to acquire in vivo real-time and ex vivo images of atherosclerotic lesions in apo E-knockout mice without contrast agents or staining. Methods: In the five apo E-knockout mice (apo E-/-, 12, 24, 32, 48, 62-week-old, 3 males) and age/sex matched five wild type mice on cow diets, we acquired in vivo real-time images of thoracic aorta without contrast agents and then, the central arterial trees were dissected intact. Ex vivo synchrotron images with tomographic reconstruction were done and compared with the corresponding pathology. Results: For all living animals, in vivo real-time images of thoracic aorta could be acquired without contrast agents but could not identify the atherosclerotic lesions. Ex vivo images accurately determined aortic wall and atherosclerotic plaque without staining in comparison to histopathology according to the AHA classification (r = 0.84, p < 0.001). The volume rendered 3 D images of plaque showed central cholesterol clefts as matched with optical images. Conclusions: The combination of synchrotron enhanced X-ray microscopy and genetically engineered hyperlipidemic animals would be a useful tool to investigate the changes of advanced atherosclerotic lesions.",
keywords = "Apo E-knockout mouse, Atherosclerosis, Plaque, Synchrotron, Unmonochromatized",
author = "Kim, {Jin Won} and Seo, {Hong Seog} and Y. Hwu and Je, {Jung Ho} and Aeree Kim and Oh, {Chil Hwan} and Suh, {Soon Yong} and Seung-Woon Rha and Park, {Chang Gyu} and Oh, {Dong Joo}",
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T1 - In vivo real-time vessel imaging and ex vivo 3D reconstruction of atherosclerotic plaque in apolipoprotein E-knockout mice using synchrotron radiation microscopy

AU - Kim, Jin Won

AU - Seo, Hong Seog

AU - Hwu, Y.

AU - Je, Jung Ho

AU - Kim, Aeree

AU - Oh, Chil Hwan

AU - Suh, Soon Yong

AU - Rha, Seung-Woon

AU - Park, Chang Gyu

AU - Oh, Dong Joo

PY - 2007/1/8

Y1 - 2007/1/8

N2 - Background: To examine the pathophysiology of atherosclerosis, imaging the vascular wall and pathology without tissue damage is required. We used the unmonochromatized synchrotron X-ray to acquire in vivo real-time and ex vivo images of atherosclerotic lesions in apo E-knockout mice without contrast agents or staining. Methods: In the five apo E-knockout mice (apo E-/-, 12, 24, 32, 48, 62-week-old, 3 males) and age/sex matched five wild type mice on cow diets, we acquired in vivo real-time images of thoracic aorta without contrast agents and then, the central arterial trees were dissected intact. Ex vivo synchrotron images with tomographic reconstruction were done and compared with the corresponding pathology. Results: For all living animals, in vivo real-time images of thoracic aorta could be acquired without contrast agents but could not identify the atherosclerotic lesions. Ex vivo images accurately determined aortic wall and atherosclerotic plaque without staining in comparison to histopathology according to the AHA classification (r = 0.84, p < 0.001). The volume rendered 3 D images of plaque showed central cholesterol clefts as matched with optical images. Conclusions: The combination of synchrotron enhanced X-ray microscopy and genetically engineered hyperlipidemic animals would be a useful tool to investigate the changes of advanced atherosclerotic lesions.

AB - Background: To examine the pathophysiology of atherosclerosis, imaging the vascular wall and pathology without tissue damage is required. We used the unmonochromatized synchrotron X-ray to acquire in vivo real-time and ex vivo images of atherosclerotic lesions in apo E-knockout mice without contrast agents or staining. Methods: In the five apo E-knockout mice (apo E-/-, 12, 24, 32, 48, 62-week-old, 3 males) and age/sex matched five wild type mice on cow diets, we acquired in vivo real-time images of thoracic aorta without contrast agents and then, the central arterial trees were dissected intact. Ex vivo synchrotron images with tomographic reconstruction were done and compared with the corresponding pathology. Results: For all living animals, in vivo real-time images of thoracic aorta could be acquired without contrast agents but could not identify the atherosclerotic lesions. Ex vivo images accurately determined aortic wall and atherosclerotic plaque without staining in comparison to histopathology according to the AHA classification (r = 0.84, p < 0.001). The volume rendered 3 D images of plaque showed central cholesterol clefts as matched with optical images. Conclusions: The combination of synchrotron enhanced X-ray microscopy and genetically engineered hyperlipidemic animals would be a useful tool to investigate the changes of advanced atherosclerotic lesions.

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