Department of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Japan; Department of Patho-Functional Bioanalysis, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.
Department of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Atherosclerosis. 2018 Aug;275:1-10. doi: 10.1016/j.atherosclerosis.2018.05.028. Epub 2018 May 18.
Macrophages are key factors in the formation of unstable atherosclerotic plaques, which may be identified through macrophage imaging. We tested whether activatable fluorescence probes of iron oxide nanoparticles (IONPs) conjugated with indocyanine green (ICG) (IONP-ICG), consisting of biocompatible reagents, can visualize macrophages present in atherosclerotic plaques.
IONP-based probes conjugated with different numbers of ICG molecules were synthesized. Six-week-old spontaneously hyperlipidemic (SHL) mice were fed either a Western or normal diet for 14 weeks, and were intravenously injected with IONP-ICG (55.8 mg Fe/kg). Aortas were harvested 48 h later, and aortas containing atherosclerotic plaques were imaged.
Phantom imaging studies using IONP-ICG solution demonstrated that the addition of surfactants to IONP-ICG solutions yielded fluorescence activation. Incubation of macrophages with IONP-ICG led to internalization of IONP-ICG and near infrared fluorescence (NIRF) activation. In NIRF imaging studies, intense fluorescence signals were clearly visible primarily at the margins of atherosclerotic plaques, and relatively weak signals were evident inside the plaques, demonstrating the feasibility of detection of NIRF signals at atherosclerotic plaques. In the quantitative evaluation of NIRF, administration of a probe conjugated with more ICG molecules led to a significant increase in the NIRF signal, indicating that probes with greater numbers of ICG molecules are effective for sensitive NIRF detection. SHL mice given a low-cholesterol normal diet showed a significantly lower NIRF signal compared with mice given the Western diet. Histologically, NIRF signals in atherosclerotic plaques strongly correlated with the location of macrophages, suggesting the possibility of NIRF macrophage imaging using IONP-ICG.
Localization of macrophages in atherosclerotic plaques may be achieved using the activatable NIRF probe, IONP-ICG.
巨噬细胞是不稳定粥样斑块形成的关键因素,可通过巨噬细胞成像进行识别。我们检测了由生物相容性试剂组成的氧化铁纳米粒子(IONP)与吲哚菁绿(ICG)偶联的可激活荧光探针(IONP-ICG)是否可以对动脉粥样硬化斑块中的巨噬细胞进行可视化。
合成了不同数量 ICG 分子偶联的基于 IONP 的探针。将 6 周龄自发性高脂血症(SHL)小鼠分别用西方饮食或正常饮食喂养 14 周,然后静脉注射 IONP-ICG(55.8mgFe/kg)。48 小时后收获主动脉,并对含有动脉粥样硬化斑块的主动脉进行成像。
使用 IONP-ICG 溶液进行的体模成像研究表明,向 IONP-ICG 溶液中添加表面活性剂可产生荧光激活。巨噬细胞与 IONP-ICG 孵育导致 IONP-ICG 的内化和近红外荧光(NIRF)激活。在 NIRF 成像研究中,强烈的荧光信号主要在动脉粥样硬化斑块的边缘清晰可见,而斑块内部的信号相对较弱,表明在动脉粥样硬化斑块处检测到 NIRF 信号是可行的。在 NIRF 的定量评估中,与偶联较少 ICG 分子的探针相比,偶联更多 ICG 分子的探针导致 NIRF 信号显著增加,表明具有更多 ICG 分子的探针对于灵敏的 NIRF 检测是有效的。给予低胆固醇正常饮食的 SHL 小鼠与给予西方饮食的小鼠相比,NIRF 信号显著降低。组织学上,动脉粥样硬化斑块中的 NIRF 信号与巨噬细胞的位置强烈相关,表明使用 IONP-ICG 进行 NIRF 巨噬细胞成像的可能性。
使用可激活的 NIRF 探针 IONP-ICG 可以实现动脉粥样硬化斑块中巨噬细胞的定位。