ULB-Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles (ULB), Route de Lennik, Brussels 808-CP618, 1070 Brussels, Belgium.
Laboratoire G-Time, Université Libre de Bruxelles (ULB), Av. F.D. Roosevelt 50 CP 160/02, 1050 Brussels, Belgium.
Molecules. 2018 Aug 21;23(9):2100. doi: 10.3390/molecules23092100.
Non-invasive imaging and quantification of human beta cell mass remains a major challenge. We performed pre-clinical in vivo validation of a peptide previously discovered by our group, namely, P88 that targets a beta cell specific biomarker, FXYD2γa. We conjugated P88 with DOTA and then complexed it with GdCl₃ to obtain the MRI (magnetic resonance imaging) contrast agent (CA) Gd-DOTA-P88. A scrambled peptide was used as a negative control CA, namely Gd-DOTA-Scramble. The CAs were injected in immunodeficient mice implanted with EndoC-βH1 cells, a human beta cell line that expresses FXYD2γa similarly to primary human beta cells. The xenograft-bearing mice were analyzed by MRI. At the end, the mice were euthanized and the CA biodistribution was evaluated on the excised tissues by measuring the Gd concentration with inductively coupled plasma mass spectrometry (ICP-MS). The MRI and biodistribution studies indicated that Gd-DOTA-P88 accumulates in EndoC-βH1 xenografts above the level observed in the background tissue, and that its uptake is significantly higher than that observed for Gd-DOTA-Scramble. In addition, the Gd-DOTA-P88 showed good xenograft-to-muscle and xenograft-to-liver uptake ratios, two potential sites of human islets transplantation. The CA shows good potential for future use to non-invasively image implanted human beta cells.
人类β细胞质量的无创成像和定量仍然是一个主要挑战。我们对我们小组先前发现的一种肽(即靶向β细胞特异性生物标志物 FXYD2γa 的 P88)进行了临床前体内验证。我们将 P88 与 DOTA 缀合,然后将其与 GdCl₃ 络合以获得 MRI(磁共振成像)造影剂(CA)Gd-DOTA-P88。将 scrambled peptide 用作阴性对照 CA,即 Gd-DOTA-Scramble。将 CA 注射到植入 EndoC-βH1 细胞的免疫缺陷小鼠中,EndoC-βH1 细胞是一种表达 FXYD2γa 的人β细胞系,其表达方式与原代人β细胞相似。通过 MRI 分析异种移植小鼠。最后,安乐死小鼠并通过电感耦合等离子体质谱法(ICP-MS)测量铽浓度评估切除组织中的 CA 生物分布。MRI 和生物分布研究表明,Gd-DOTA-P88 在背景组织中观察到的水平之上在 EndoC-βH1 异种移植瘤中积累,并且其摄取量明显高于 Gd-DOTA-Scramble。此外,Gd-DOTA-P88 显示出良好的异种移植瘤与肌肉和异种移植瘤与肝脏摄取比,这是人类胰岛移植的两个潜在部位。该 CA 具有良好的非侵入性成像植入的人类β细胞的未来应用潜力。