TRPM7-Mediated Calcium Transport in HAT-7 Ameloblasts

• Published in: International journal of molecular sciences Vol. 22; no. 8; p. 3992
• Main Authors: Kádár, Kristóf, Juhász, Viktória, Földes, Anna, Rácz, Róbert, Zhang, Yan, Löchli, Heike, Kató, Erzsébet, Köles, László, Steward, Martin C, DenBesten, Pamela, Varga, Gábor, Zsembery, Ákos
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13.04.2021; MDPI
• Subjects: Ameloblasts; Ameloblasts - cytology; Ameloblasts - drug effects; Ameloblasts - metabolism; amelogenesis; Anilides - pharmacology; Animals; Calcium - metabolism; Calcium channels; calcium entry; Calcium homeostasis; Calcium influx; Calcium ions; Calcium transport; Cell Line; Channels; Dental enamel; enamel; FTY720; Gene expression; Homeostasis; Humans; Hydrogen-Ion Concentration; Incisor - cytology; Intracellular; Ion Channel Gating - drug effects; Ion Transport - drug effects; Kinases; Magnesium; Mibefradil - pharmacology; Mice; Mineralization; Models, Biological; mRNA; Naltrexone - analogs & derivatives; Naltrexone - pharmacology; Physiology; Protein expression; Proteins; Rats; Thiadiazoles - pharmacology; Transient receptor potential proteins; TRPM Cation Channels - metabolism; TRPM7 channel protein; calcium entry; TRPM7 channel protein; store-operated calcium entry; pH; enamel; magnesium; amelogenesis
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22083992

TRPM7 plays an important role in cellular Ca , Zn and Mg homeostasis. TRPM7 channels are abundantly expressed in ameloblasts and, in the absence of TRPM7, dental enamel is hypomineralized. The potential role of TRPM7 channels in Ca transport during amelogenesis was investigated in the HAT-7 rat ameloblast cell line. The cells showed strong TRPM7 mRNA and protein expression. Characteristic TRPM7 transmembrane currents were observed, which increased in the absence of intracellular Mg ([Mg ] ), were reduced by elevated [Mg ] , and were inhibited by the TRPM7 inhibitors NS8593 and FTY720. Mibefradil evoked similar currents, which were suppressed by elevated [Mg ] , reducing extracellular pH stimulated transmembrane currents, which were inhibited by FTY720. Naltriben and mibefradil both evoked Ca influx, which was further enhanced by the acidic intracellular conditions. The SOCE inhibitor BTP2 blocked Ca entry induced by naltriben but not by mibefradil. Thus, in HAT-7 cells, TRPM7 may serves both as a potential modulator of Orai-dependent Ca uptake and as an independent Ca entry pathway sensitive to pH. Therefore, TRPM7 may contribute directly to transepithelial Ca transport in amelogenesis.