首页> 美国卫生研究院文献>Neoplasia (New York N.Y.) >Magnetic Resonance Imaging Detection of Tumor Cells by Targeting Low-Density Lipoprotein Receptors with Gd-Loaded Low-Density Lipoprotein Particles
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Magnetic Resonance Imaging Detection of Tumor Cells by Targeting Low-Density Lipoprotein Receptors with Gd-Loaded Low-Density Lipoprotein Particles

机译:靶向Gd负载的低密度脂蛋白颗粒的低密度脂蛋白受体的磁共振成像检测肿瘤细胞

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摘要

Gd-DO3A-diph and Gd-AAZTAC17 are lipophilic magnetic resonance imaging (MRI) agents that display high affinity for low-density lipoprotein (LDL) particles. However, on binding to LDL, Gd-DO3A-diph shows a decreased hydration that results in a lower enhancement of water proton relaxation rate. Conversely, Gd-AAZTAC17 displays a strong relaxation enhancement at the imaging fields. Each LDL particle can load up to 100 and 400 UNITS of Gd-DO3A-diph and Gd-AAZTAC17, respectively. Their LDL adducts are taken up by human hepatoblastoma G2 (HepG2) and melanoma B16 tumor cells when added to the incubation medium. T1 measurements of the labeled cells indicate that Gd-AAZTAC17 is significantly more efficient than Gd-DO3A-diph. Furthermore, it has been found that HepG2 hepatoma cells can internalize higher amounts of Gd-AAZTAC17 than B16 cells and the involvement of LDL receptors (LDLRs) has been demonstrated in competition assays with free LDL. Gd-AAZTAC17/LDL adduct proved to be an efficient probe in the magnetic resonance (MR) visualization of subcutaneous tumors in animal models obtained by injecting B16 melanoma cells into the right flank of mice. Finally, confocal microscopy validation of the distribution of LDL-based probes in the tumor has been obtained by doping the Gd-AAZTAC17/LDL adduct with a fluorescent phospholipid moiety.
机译:Gd-DO3A-diph和Gd-AAZTAC17是亲脂性磁共振成像(MRI)剂,对低密度脂蛋白(LDL)颗粒显示出高亲和力。但是,与LDL结合时,Gd-DO3A-diph的水合作用降低,从而导致水质子弛豫速率降低。相反,Gd-AAZTAC17在成像场显示出很强的弛豫增强。每个LDL颗粒分别可装载多达100单位和400单位的Gd-DO3A-diph和Gd-AAZTAC17。加入培养液后,它们的LDL加合物被人肝母细胞瘤G2(HepG2)和黑色素瘤B16肿瘤细胞吸收。标记细胞的T1测量表明,Gd-AAZTAC17比Gd-DO3A-diph更有效。此外,已经发现,HepG2肝癌细胞可以比B16细胞内化更多量的Gd-AAZTAC17,并且在与游离LDL的竞争测定中已经证明了LDL受体(LDLR)的参与。 Gd-AAZTAC17 / LDL加合物被证明是在动物模型中皮下肿瘤的磁共振(MR)可视化研究中的有效探针,该动物模型是通过将B16黑色素瘤细胞注射到小鼠的右侧腹而获得的。最后,通过用荧光磷脂部分掺杂Gd-AAZTAC17 / LDL加合物获得了基于LDL的探针在肿瘤中分布的共聚焦显微镜验证。

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