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Optical control of the nuclear bile acid receptor FXR with a photohormone

Herein, we report a photoswitchable modulator for a nuclear hormone receptor that exerts its hormonal effects in a light-dependent fashion. The azobenzene AzoGW enables optical control of the farnesoid X receptor (FXR), a key regulator of hepatic bile acid, lipid and glucose metabolism. AzoGW was de...

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Autores principales: Morstein, Johannes, Trads, Julie B., Hinnah, Konstantin, Willems, Sabine, Barber, David M., Trauner, Michael, Merk, Daniel, Trauner, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067245/
https://www.ncbi.nlm.nih.gov/pubmed/32190263
http://dx.doi.org/10.1039/c9sc02911g
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author Morstein, Johannes
Trads, Julie B.
Hinnah, Konstantin
Willems, Sabine
Barber, David M.
Trauner, Michael
Merk, Daniel
Trauner, Dirk
author_facet Morstein, Johannes
Trads, Julie B.
Hinnah, Konstantin
Willems, Sabine
Barber, David M.
Trauner, Michael
Merk, Daniel
Trauner, Dirk
author_sort Morstein, Johannes
collection PubMed
description Herein, we report a photoswitchable modulator for a nuclear hormone receptor that exerts its hormonal effects in a light-dependent fashion. The azobenzene AzoGW enables optical control of the farnesoid X receptor (FXR), a key regulator of hepatic bile acid, lipid and glucose metabolism. AzoGW was derived from the synthetic agonist GW4064 through an azologization strategy and is a metabolically stable, highly selective photoswitchable FXR agonist in its dark-adapted form. Upon irradiation, the thermally bistable ‘photohormone’ becomes significantly less active. Optical control of FXR was demonstrated in a luminescence reporter gene assay and through light-dependent reversible transcription modulation of FXR target genes (CYP7A1, Ostα, Ostβ) in liver cells.
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spelling pubmed-70672452020-03-18 Optical control of the nuclear bile acid receptor FXR with a photohormone Morstein, Johannes Trads, Julie B. Hinnah, Konstantin Willems, Sabine Barber, David M. Trauner, Michael Merk, Daniel Trauner, Dirk Chem Sci Chemistry Herein, we report a photoswitchable modulator for a nuclear hormone receptor that exerts its hormonal effects in a light-dependent fashion. The azobenzene AzoGW enables optical control of the farnesoid X receptor (FXR), a key regulator of hepatic bile acid, lipid and glucose metabolism. AzoGW was derived from the synthetic agonist GW4064 through an azologization strategy and is a metabolically stable, highly selective photoswitchable FXR agonist in its dark-adapted form. Upon irradiation, the thermally bistable ‘photohormone’ becomes significantly less active. Optical control of FXR was demonstrated in a luminescence reporter gene assay and through light-dependent reversible transcription modulation of FXR target genes (CYP7A1, Ostα, Ostβ) in liver cells. Royal Society of Chemistry 2019-11-19 /pmc/articles/PMC7067245/ /pubmed/32190263 http://dx.doi.org/10.1039/c9sc02911g Text en This journal is © The Royal Society of Chemistry 2020 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Morstein, Johannes
Trads, Julie B.
Hinnah, Konstantin
Willems, Sabine
Barber, David M.
Trauner, Michael
Merk, Daniel
Trauner, Dirk
Optical control of the nuclear bile acid receptor FXR with a photohormone
title Optical control of the nuclear bile acid receptor FXR with a photohormone
title_full Optical control of the nuclear bile acid receptor FXR with a photohormone
title_fullStr Optical control of the nuclear bile acid receptor FXR with a photohormone
title_full_unstemmed Optical control of the nuclear bile acid receptor FXR with a photohormone
title_short Optical control of the nuclear bile acid receptor FXR with a photohormone
title_sort optical control of the nuclear bile acid receptor fxr with a photohormone
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067245/
https://www.ncbi.nlm.nih.gov/pubmed/32190263
http://dx.doi.org/10.1039/c9sc02911g
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