De Saint-Hubert M, Bauwens M, Deckers N, Drummen M, Douma K, Granton P, Hendrikx G, Kusters D, Bucerius J, Reutelingsperger C P M, Mottaghy F M
Department of Nuclear Medicine, MUMC, Maastricht, The Netherlands,
Mol Imaging Biol. 2014 Apr;16(2):246-54. doi: 10.1007/s11307-013-0677-0.
The purpose of this paper is to study molecular imaging of apoptosis and necrosis, two key players in atherosclerosis instability, using a multimodal imaging approach combining single photon emission computed tomography (SPECT), positron emission tomography (PET), and computed tomography (CT).
Collar-induced carotid atherosclerosis ApoE knockout mice were imaged with (99m)Tc-AnxAF568 SPECT-CT to study apoptosis and sequentially with PET-CT following (124)I-Hypericin ((124)I-Hyp) injection to visualize necrosis.
SPECT depicted increased (99m)Tc-AnxAF568 uptake in both atherosclerotic carotid arteries, whereas our data suggest that this uptake is not merely apoptosis related. Although PET of (124)I-Hyp was hampered by the slow blood clearance in atherosclerotic mice, (124)I-Hyp was able to target necrosis in the atherosclerotic plaque.
Both (99m)Tc-AnxAF568 and (124)I-Hyp uptake are increased in atherosclerotic carotid vasculature compared to control arteries. While apoptosis imaging remains challenging, necrosis imaging can be feasible after improving the biodistribution characteristics of the probe.
本文的目的是使用单光子发射计算机断层扫描(SPECT)、正电子发射断层扫描(PET)和计算机断层扫描(CT)相结合的多模态成像方法,研究动脉粥样硬化不稳定性的两个关键因素——细胞凋亡和坏死的分子成像。
对套环诱导的颈动脉粥样硬化载脂蛋白E基因敲除小鼠进行(99m)Tc-AnxAF568 SPECT-CT成像以研究细胞凋亡,并在注射(124)I-金丝桃素((124)I-Hyp)后依次进行PET-CT成像以观察坏死情况。
SPECT显示两条动脉粥样硬化颈动脉中(99m)Tc-AnxAF568摄取增加,然而我们的数据表明这种摄取不仅仅与细胞凋亡有关。尽管(124)I-Hyp的PET成像受到动脉粥样硬化小鼠血液清除缓慢的阻碍,但(124)I-Hyp能够靶向动脉粥样硬化斑块中的坏死区域。
与对照动脉相比,动脉粥样硬化颈动脉血管中(99m)Tc-AnxAF568和(124)I-Hyp的摄取均增加。虽然细胞凋亡成像仍然具有挑战性,但在改善探针的生物分布特性后,坏死成像可能是可行的。