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Bertrand, R.* ; Wolf, A.* ; Ivashchenko, Y.* ; Löhn, M.* ; Schäfer, M.* ; Brönstrup, M.* ; Gotthardt, M.* ; Derdau, V.* ; Plettenburg, O.

Synthesis and characterization of a promising novel FFAR1/GPR40 targeting fluorescent probe for β-cell imaging.

ACS Chem. Biol. 11, 1745-1754 (2016)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Diabetes affects an increasing number of patients worldwide and is responsible for a significant rise in healthcare expenses. Imaging of β-cells bears the potential to contribute to an improved understanding, diagnosis, and development of new treatment options for diabetes. Here, we describe the first small molecule fluorescent probe targeting the free fatty acid receptor 1 (FFAR1/GPR40). This receptor is highly expressed on β-cells, and was up to now unexplored for imaging purposes. We designed a novel probe by facile modification of the selective and potent FFAR1 agonist TAK-875. Effective and specific binding of the probe was demonstrated using FFAR1 overexpressing cells. We also successfully labeled FFAR1 on MIN6 and INS1E cells, two widely used β-cell models, by applying an effective amplification protocol. Finally, we showed that the probe is capable of inducing insulin secretion in a glucose-dependent manner, thus demonstrating that functional activity of the probe was maintained. These results suggest that our probe represents a first important step to successful β-cell imaging by targeting FFAR1. The developed probe may prove to be particularly useful for in vitro and ex vivo studies of diabetic cellular and animal models to gain new insights into disease pathogenesis.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Acid Receptor 1; Type-2 Diabetes-mellitus; Free Fatty-acids; Mass In-vivo; Insulin-secretion; Down-regulation; Double-blind; Gpr40; Agonist; Tak-875
ISSN (print) / ISBN 1554-8929
e-ISSN 1554-8937
Zeitschrift ACS Chemical Biology
Quellenangaben Band: 11, Heft: 6, Seiten: 1745-1754 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Verlagsort Washington
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Medicinal Chemistry (IMC)