Chris J van Koppen
Mechanism of Action of a Nanomolar Potent, Allosteric Antagonist of the Thyroid-Stimulating Hormone Receptor
van Koppen, Chris J; de Gooyer, Marcel E; Karstens, Willem-Jan; Plate, Ralf; Conti, Paolo G M; van Achterberg, Tanja A E; van Amstel, Monique G A; Brands, Jolanda H G M; Wat, Jesse; Berg, Rob J W; Lane, J Robert D; Miltenburg, Andre M M; Timmers, C Marco
Authors
Marcel E de Gooyer
Willem-Jan Karstens
Ralf Plate
Paolo G M Conti
Tanja A E van Achterberg
Monique G A van Amstel
Jolanda H G M Brands
Jesse Wat
Rob J W Berg
J Robert D Lane
Andre M M Miltenburg
C Marco Timmers
Abstract
Background and purpose Graves' disease (GD) is an autoimmune disease in which the thyroid is overactive, producing excessive amounts of thyroid hormones, caused by TSHR-stimulating immunoglobulins (TSIs). A large proportion of GD patients also suffer from thyroid eye disease (Graves' ophthalmopathy or GO), with the TSIs considered to activate TSHRs in orbital tissue also. We recently developed LMW TSHR antagonists as a novel therapeutic strategy for the treatment of GD and GO. In the present study, we determined the molecular pharmacology of a prototypic, nanomolar potent LMW TSHR antagonist, Org 274179-0. Experimental approach First, we determined the potency and efficacy of Org 274179-0 in antagonizing TSH- and TSI-induced TSHR signaling and its cross-reactivity at the related FSHR and LHR. Second, we explored in depth the allosteric mode of interaction of Org 274179-0. Third, we determined whether Org 274179-0 is an inverse agonist at five naturally occurring, constitutively active TSHR mutants. Key results Org 274179-0 fully inhibited TSH (and TSI)-mediated TSHR activation with nanomolar potency without hardly affecting the potency of TSH, in accordance with an allosteric mechanism of action. On the reverse, increasing levels of TSHR stimulation only marginally reduced the antagonistic potency of Org 274179-0. Finally, Org 274179-0 fully blocked the increased basal activity of all tested constitutively active TSHR mutants with nanomolar potencies. Conclusions and implications We conclude that nanomolar potent TSHR antagonists like Org 274179-0 have the potential of being developed to treat GD and GO.
Citation
van Koppen, C. J., de Gooyer, M. E., Karstens, W.-J., Plate, R., Conti, P. G. M., van Achterberg, T. A. E., van Amstel, M. G. A., Brands, J. H. G. M., Wat, J., Berg, R. J. W., Lane, J. R. D., Miltenburg, A. M. M., & Timmers, C. M. (2012). Mechanism of Action of a Nanomolar Potent, Allosteric Antagonist of the Thyroid-Stimulating Hormone Receptor. British Journal of Pharmacology, 165(7), 2314-2324. https://doi.org/10.1111/j.1476-5381.2011.01709.x
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 15, 2011 |
Online Publication Date | Oct 20, 2011 |
Publication Date | 2012-04 |
Deposit Date | Apr 22, 2020 |
Journal | British Journal of Pharmacology |
Print ISSN | 0007-1188 |
Electronic ISSN | 1476-5381 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 165 |
Issue | 7 |
Pages | 2314-2324 |
DOI | https://doi.org/10.1111/j.1476-5381.2011.01709.x |
Public URL | https://nottingham-repository.worktribe.com/output/1339713 |
Publisher URL | https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1111/j.1476-5381.2011.01709.x |
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