Data

L-amino acids promote calcitonin release via a calcium-sensing receptor: Gq/11-mediated pathway in human C-cells: supplemental figures

The University of Sydney
Arthur Conigrave (Principal investigator)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=http://hdl.handle.net/2123/20259&rft.title=L-amino acids promote calcitonin release via a calcium-sensing receptor: Gq/11-mediated pathway in human C-cells: supplemental figures&rft.identifier= http://hdl.handle.net/2123/20259&rft.publisher=The University of Sydney&rft.description=Human calcitonin release is promoted by elevated extracellular Ca2+ (Ca2+o) concentration acting, at least in part,via the calcium-sensing receptor (CaSR). The CaSR is positively modulated by L-amino acids including the aromaticamino acids L-Phe and L-Trp. To investigate the effect of L-amino acids on human calcitonin secretion we selectedthyroid TT cells and exposed them to various Ca2+o concentrations in the absence or presence of L-Phe, plasma-likemixtures of L-amino acids, or the clinically effective positive modulator (calcimimetic), cinacalcet. In the presence ofL-Phe or plasma-like mixtures of amino acids, TT cells exhibited enhanced Ca2+o sensitivity in assays of calcitoninrelease and intracellular Ca2+ (Ca2+i) mobilization. Furthermore, the effect of elevated Ca2+o and L-Phe oncalcitonin release was markedly suppressed by the calcilytic NPS-2143. These effects were dependent uponCaSR-mediated activation of Gq/11 as revealed by the specific inhibitor YM-254890. The findings support thehypothesis that calcitonin release is stimulated by increases in plasma L-amino acid levels as well as elevatedextracellular Ca2+. They also demonstrate that stimulated calcitonin release as well as basal levels of calcitoninsecretion are mediated by a CaSR:Gq/11 signaling mechanism. This dataset comprises of 4 files; two supplemental figures, methods for supplemental figures document, and supplemental figure legends.&rft.creator=Arthur Conigrave&rft.date=2019&rft_rights= PDDL: Public Domain Dedication and License 1.0 https://opendatacommons.org/licenses/pddl/1.0/index.html&rft_subject=MEDICAL BIOCHEMISTRY AND METABOLOMICS&rft_subject=MEDICAL AND HEALTH SCIENCES&rft_subject=PHARMACOLOGY AND PHARMACEUTICAL SCIENCES&rft.type=dataset&rft.language=English

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Brief description

Human calcitonin release is promoted by elevated extracellular Ca2+ (Ca2+o) concentration acting, at least in part,
via the calcium-sensing receptor (CaSR). The CaSR is positively modulated by L-amino acids including the aromatic
amino acids L-Phe and L-Trp. To investigate the effect of L-amino acids on human calcitonin secretion we selected
thyroid TT cells and exposed them to various Ca2+o concentrations in the absence or presence of L-Phe, plasma-like
mixtures of L-amino acids, or the clinically effective positive modulator (calcimimetic), cinacalcet. In the presence of
L-Phe or plasma-like mixtures of amino acids, TT cells exhibited enhanced Ca2+o sensitivity in assays of calcitonin
release and intracellular Ca2+ (Ca2+i) mobilization. Furthermore, the effect of elevated Ca2+o and L-Phe on
calcitonin release was markedly suppressed by the calcilytic NPS-2143. These effects were dependent upon
CaSR-mediated activation of Gq/11 as revealed by the specific inhibitor YM-254890. The findings support the
hypothesis that calcitonin release is stimulated by increases in plasma L-amino acid levels as well as elevated
extracellular Ca2+. They also demonstrate that stimulated calcitonin release as well as basal levels of calcitonin
secretion are mediated by a CaSR:Gq/11 signaling mechanism.

This dataset comprises of 4 files; two supplemental figures, methods for supplemental figures document, and supplemental figure legends.

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Identifiers
ACN 633 798 857