Functional characterization of olfactory receptors in the thyroid gland

  • Olfactory receptors (ORs) are almost ubiquitously expressed in the human body. However, information about their functions in these tissues is lacking. To date, no functional characterization of expressed ORs in the human thyroid has been performed. In this study, we detected and compared the expression of OR2H2 and OR2W3 in healthy and malignant cell lines and their corresponding tissues, respectively. We demonstrated that stimulation of ORs by their specific ligand resulted in a transient increase in intracellular calcium and cAMP concentrations. In the case of OR2H2, the downstream signaling cascade analysis revealed that adenylate cyclase (AC) and phosphoinositide phospholipase C (PLC) were involved. Furthermore, OR2H2 and OR2W3 activation affected migration, proliferation, and invasion. These are the first insights that ORs influence physiology-relevant processes in the healthy and malignant thyroid.

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Metadaten
Author:Daniel WeidingerGND, Nikolina JovancevicGND, Denise ZwanzigerORCiDGND, Sarah TheurerGND, Judith HönesGND, Dagmar FührerGND, Hanns HattGND
URN:urn:nbn:de:hbz:294-87682
DOI:https://doi.org/10.3389/fphys.2021.676907
Parent Title (English):Frontiers in physiology
Publisher:Frontiers
Place of publication:Lausanne
Document Type:Article
Language:English
Date of Publication (online):2022/03/24
Date of first Publication:2021/07/27
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Open Access Fonds
CRISPR/Cas9; G protein-coupled receptor; calcium imaging; olfactory receptor; thyroid cancer
Volume:12
Issue:Article 676907
First Page:676907-1
Last Page:676907-12
Note:
Article Processing Charge funded by the Open Access Publication Fund of Ruhr-Universität Bochum.
Institutes/Facilities:Lehrstuhl für Zellphysiologie
Dewey Decimal Classification:Naturwissenschaften und Mathematik / Biowissenschaften, Biologie, Biochemie
open_access (DINI-Set):open_access
Licence (English):License LogoCreative Commons - CC BY 4.0 - Attribution 4.0 International