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Shining Light and Illuminating Murine Atherosclerosis via Optical Coherence Tomography
Author(s) -
Farouc A. Jaffer
Publication year - 2012
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.246439
Subject(s) - optical coherence tomography , optics , physics
> “Better to illuminate than merely to shine, to deliver to others contemplated truths than merely to contemplate.” > > –Saint Thomas AquinasIn vivo visualization and quantification of plaque burden and plaque macrophages are major goal in the field of atherosclerosis imaging, particularly in highly utilized mouse models of atherosclerosis. Thus far, vascular MRI has demonstrated the ability to quantify and track murine atherosclerosis at moderate resolution.1,2 In addition, molecular imaging approaches have illuminated plaque macrophages in vivo.3,4 However, only a few approaches, such as intravital fluorescence microscopy, have provided high-resolution (<100 micrometer) imaging of plaque macrophages in murine atherosclerosis.5,6 Intravital fluorescence microscopy imaging, however, is limited by light penetration and is also impractical to use for comprehensive aortic imaging, a major zone of atherosclerosis in genetically altered mice.See accompanying article on page 1150In this issue of Arteriosclerosis, Thrombosis, and Vascular Biology, …

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