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In Vivo Visualization of ß-Cells by Targeting of GPR44.
Eriksson, Olof; Johnström, Peter; Cselenyi, Zsolt; Jahan, Mahabuba; Selvaraju, Ram K; Jensen-Waern, Marianne; Takano, Akihiro; Sörhede Winzell, Maria; Halldin, Christer; Skrtic, Stanko; Korsgren, Olle.
Afiliação
  • Eriksson O; Division of Molecular Imaging, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden olof.eriksson@pet.medchem.uu.se.
  • Johnström P; Personalised Healthcare and Biomarkers, AstraZeneca PET Science Centre, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Cselenyi Z; Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
  • Jahan M; Personalised Healthcare and Biomarkers, AstraZeneca PET Science Centre, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Selvaraju RK; Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
  • Jensen-Waern M; Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
  • Takano A; Division of Molecular Imaging, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
  • Sörhede Winzell M; Department of Clinical Sciences, Swedish University of Agricultural Sciences, Uppsala, Sweden.
  • Halldin C; Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
  • Skrtic S; AstraZeneca R&D, Mölndal, Sweden.
  • Korsgren O; Department of Clinical Neuroscience, Center for Psychiatry Research, Karolinska Institutet and Stockholm County Council, Stockholm, Sweden.
Diabetes ; 67(2): 182-192, 2018 02.
Article em En | MEDLINE | ID: mdl-29208633
ABSTRACT
GPR44 expression has recently been described as highly ß-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 ß-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 ß-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 ß-cells by targeting the protein GPR44.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Éteres Fenílicos / Receptores de Prostaglandina / Receptores Imunológicos / Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Éteres Fenílicos / Receptores de Prostaglandina / Receptores Imunológicos / Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article