Division of Molecular Imaging, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden
Personalised Healthcare and Biomarkers, AstraZeneca PET Science Centre, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Diabetes. 2018 Feb;67(2):182-192. doi: 10.2337/db17-0764. Epub 2017 Dec 5.
GPR44 expression has recently been described as highly β-cell selective in the human pancreas and constitutes a tentative surrogate imaging biomarker in diabetes. A radiolabeled small-molecule GPR44 antagonist, [C]AZ12204657, was evaluated for visualization of β-cells in pigs and nonhuman primates by positron emission tomography as well as in immunodeficient mice transplanted with human islets under the kidney capsule. In vitro autoradiography of human and animal pancreatic sections from subjects without and with diabetes, in combination with insulin staining, was performed to assess β-cell selectivity of the radiotracer. Proof of principle of in vivo targeting of human islets by [C]AZ12204657 was shown in the immunodeficient mouse transplantation model. Furthermore, [C]AZ12204657 bound by a GPR44-mediated mechanism in pancreatic sections from humans and pigs without diabetes, but not those with diabetes. In vivo [C]AZ12204657 bound specifically to GPR44 in pancreas and spleen and could be competed away dose-dependently in nondiabetic pigs and nonhuman primates. [C]AZ12204657 is a first-in-class surrogate imaging biomarker for pancreatic β-cells by targeting the protein GPR44.
GPR44 的表达在人类胰腺中被描述为高度选择性β细胞,构成了糖尿病的候选成像生物标志物。一种放射性标记的小分子 GPR44 拮抗剂 [C]AZ12204657,已在猪和非人类灵长类动物中通过正电子发射断层扫描(PET)进行了评估,以用于可视化β细胞,以及在肾包膜下移植了人类胰岛的免疫缺陷小鼠中进行了评估。对来自无糖尿病和糖尿病患者的人和动物胰腺切片进行体外放射自显影,并结合胰岛素染色,以评估示踪剂的β细胞选择性。在免疫缺陷小鼠胰岛移植模型中,证明了 [C]AZ12204657 对人胰岛的体内靶向作用。此外,[C]AZ12204657 通过人类和猪无糖尿病胰腺切片中的 GPR44 介导机制结合,但在糖尿病患者中不结合。在体内,[C]AZ12204657 特异性地结合胰腺和脾脏中的 GPR44,并且可以在非糖尿病猪和非人类灵长类动物中以剂量依赖性方式竞争掉。[C]AZ12204657 是一种通过靶向蛋白 GPR44 用于胰腺β细胞的首创类候选成像生物标志物。