Ansciaux Emilie, Burtea Carmen, Laurent Sophie, Crombez Deborah, Nonclercq Denis, Vander Elst Luce, Muller Robert N
Department of General, Organic and Biomedical Chemistry, NMR and Molecular Imaging Laboratory, University of Mons, Avenue Maistriau 19, Mendeleev Building, B-7000, Mons, Belgium.
Laboratory of Histology, University of Mons, Pentagon - 1B, 6 Avenue du Champ de Mars, B-7000, Mons, Belgium.
Contrast Media Mol Imaging. 2015 May-Jun;10(3):211-24. doi: 10.1002/cmmi.1626. Epub 2014 Oct 5.
Alzheimer's disease (AD) is a neurodegenerative disorder most often diagnosed 10 years after its onset and development. It is characterized by the accumulation of amyloid-β peptide (ABP) into amyloid plaques between nerve cells, which produces a massive local neurodegeneration. Molecular magnetic resonance imaging allows diagnosis of AD by showing ABP accumulation in the brain. The ultrasmall particles of iron oxide (USPIO) derivatives proposed in the present work were functionalized with peptides that present an affinity for ABP, independently of its state of aggregation. Their nanomolar Kd * confirms the high affinity of our vectorized contrast agents (VCA) for ABP and therefore their high labeling potential, specificity and sensitivity. Their lack of toxicity has been demonstrated, both by in vitro studies using the MTT method on several cell types, and by in vivo investigations with assessment of renal and hepatic biomarkers and by histopathology evaluation. The results of biodistribution studies corroborated by MRI demonstrate that USPIO-PHO (USPIO coupled to peptide C-IPLPFYN-C) are able to cross the blood-brain barrier without any facilitating strategy, and accumulates in the brain 90 min after its injection in NMRI mice. None of the USPIO derivatives were found in any organs one week after administration. To conclude, USPIO-PHO seems to have a genuine potential for labeling amyloid plaques in the brain; it has a nanomolar binding affinity, no toxic effects, and its elimination half-life is about 3 h. Further tests will be made on transgenic mice, aimed at confirming the potential of early AD diagnosis using our VCA.
阿尔茨海默病(AD)是一种神经退行性疾病,通常在发病和发展10年后才能被诊断出来。其特征是淀粉样β肽(ABP)在神经细胞之间聚集成淀粉样斑块,从而导致大量局部神经退行性变。分子磁共振成像通过显示大脑中ABP的积累来诊断AD。本研究中提出的超小氧化铁颗粒(USPIO)衍生物用对ABP具有亲和力的肽进行了功能化修饰,而与ABP的聚集状态无关。它们的纳摩尔解离常数(Kd*)证实了我们的靶向造影剂(VCA)对ABP具有高亲和力,因此具有高标记潜力、特异性和敏感性。通过使用MTT法对几种细胞类型进行体外研究,以及通过评估肾脏和肝脏生物标志物的体内研究和组织病理学评估,均已证明它们没有毒性。MRI证实的生物分布研究结果表明,USPIO-PHO(与肽C-IPLPFYN-C偶联的USPIO)无需任何促进策略就能穿过血脑屏障,并在注射到NMRI小鼠体内90分钟后在大脑中积累。给药一周后,在任何器官中均未发现任何USPIO衍生物。总之,USPIO-PHO似乎具有标记大脑中淀粉样斑块的真正潜力;它具有纳摩尔结合亲和力,无毒性作用且消除半衰期约为3小时。将对转基因小鼠进行进一步测试,旨在确认使用我们的VCA进行早期AD诊断的潜力。