In Vivo Visualization of β-Cells by Targeting of GPR44.
Irina VelikyanPeter JohnströmZsolt CselenyiMahabuba JahanRam K SelvarajuMarianne Jensen-WaernAkihiro TakanoMaria Sörhede WinzellChrister HalldinStanko SkrticKorsgren OllePublished in: Diabetes (2017)
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, [11C]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 [11C]AZ12204657 was shown in the immunodeficient mouse transplantation model. Furthermore, [11C]AZ12204657 bound by a GPR44-mediated mechanism in pancreatic sections from humans and pigs without diabetes, but not those with diabetes. In vivo [11C]AZ12204657 bound specifically to GPR44 in pancreas and spleen and could be competed away dose-dependently in nondiabetic pigs and nonhuman primates. [11C]AZ12204657 is a first-in-class surrogate imaging biomarker for pancreatic β-cells by targeting the protein GPR44.
Keyphrases
- type diabetes
- endothelial cells
- small molecule
- positron emission tomography
- cardiovascular disease
- glycemic control
- fatty acid
- induced pluripotent stem cells
- computed tomography
- cell therapy
- single cell
- metabolic syndrome
- adipose tissue
- poor prognosis
- cell death
- signaling pathway
- drug delivery
- pet imaging
- photodynamic therapy
- protein protein
- fluorescence imaging
- high fat diet induced