Activation of calcium-sensing receptor by allosteric agonists cinacalcet and AC-265347 abolishes the 1,25(OH)2D3-induced Ca2+ transport: Evidence that explains how the intestine prevents excessive Ca2+ absorption
Autor: | Narattaphol Charoenphandhu, Jarinthorn Teerapornpuntakit, Kannikar Wongdee, Jirawan Thongbunchoo, Walailak Jantarajit, Mayuree Rodrat, Chutiya Keadsai |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Calcium metabolism medicine.medical_specialty Cinacalcet Chemistry Allosteric regulation Biophysics chemistry.chemical_element 030209 endocrinology & metabolism Calcium Biochemistry 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Endocrinology Paracellular transport Internal medicine medicine Secretion Calcium-sensing receptor Receptor Molecular Biology medicine.drug |
Zdroj: | Archives of Biochemistry and Biophysics. 657:15-22 |
ISSN: | 0003-9861 |
DOI: | 10.1016/j.abb.2018.09.004 |
Popis: | Long-term high-calcium intake and intestinal calcium hyperabsorption are hazardous to the body. It is hypothesized that enterocytes possess mechanisms for preventing superfluous calcium absorption, including secretion of negative regulators of calcium absorption and utilization of calcium-sensing receptor (CaSR) to detect luminal calcium. Herein, Caco-2 monolayers were treated with high doses of 1,25(OH)2D3 to induce calcium hyperabsorption or directly exposed to high apical calcium. The expression of counterregulatory factor of calcium absorption, fibroblast growth factor (FGF)-23, was also investigated in the intestine of lactating rats, which physiologically exhibit calcium hyperabsorption. We found that FGF-23 expression was enhanced in all intestinal segments of lactating rats. In Caco-2 monolayers, high apical calcium and 1,25(OH)2D3 induced FGF-23 secretion into culture media. FGF-23 antagonized 1,25(OH)2D3-induced calcium transport and led to a significant, but small, change in paracellular permeability. Furthermore, high-dose 1,25(OH)2D3 upregulated FGF-23 expression, which was prevented by CaSR inhibitors. Activation of apical CaSR by cinacalcet and AC-265347 abolished 1,25(OH)2D3-induced calcium transport in a dose-dependent manner. In conclusion, the intestinal FGF-23 expression was upregulated in conditions with calcium hyperabsorption, presumably to help protect against excessive calcium absorption, while CaSR probably monitored calcium in the lumen and induced FGF-23 production for preventing superfluous calcium uptake. |
Databáze: | OpenAIRE |
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