McAteer Martina A, Choudhury Robin P
Midatech Ltd., Begbroke Science Park, Begbroke Hill, Woodstock Road, Oxfordshire, OX5 1PF, UK.
Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK.
Methods Mol Biol. 2015;1339:61-83. doi: 10.1007/978-1-4939-2929-0_4.
Molecular imaging offers great potential for noninvasive visualization and quantitation of the cellular and molecular components involved in atherosclerotic plaque stability. In this chapter, we review emerging molecular imaging modalities and approaches for quantitative, noninvasive detection of early biological processes in atherogenesis, including vascular endothelial permeability, endothelial adhesion molecule up-regulation, and macrophage accumulation, with special emphasis on mouse models. We also highlight a number of targeted imaging nanomaterials for assessment of advanced atherosclerotic plaques, including extracellular matrix degradation, proteolytic enzyme activity, and activated platelets using mouse models of atherosclerosis. The potential for clinical translation of molecular imaging nanomaterials for assessment of atherosclerotic plaque biology, together with multimodal approaches is also discussed.
分子成像为无创可视化和定量分析参与动脉粥样硬化斑块稳定性的细胞和分子成分提供了巨大潜力。在本章中,我们综述了新兴的分子成像模式和方法,用于定量、无创检测动脉粥样硬化发生过程中的早期生物学过程,包括血管内皮通透性、内皮黏附分子上调和巨噬细胞聚集,特别强调小鼠模型。我们还重点介绍了一些用于评估晚期动脉粥样硬化斑块的靶向成像纳米材料,包括使用动脉粥样硬化小鼠模型评估细胞外基质降解、蛋白水解酶活性和活化血小板。还讨论了用于评估动脉粥样硬化斑块生物学的分子成像纳米材料临床转化的潜力以及多模态方法。