Sodium-Calcium Exchangers in Rat Ameloblasts

Although the central role of ameloblasts in synthesis and resorption of enamel matrix proteins during amelogenesis is well documented, the Ca2+-transport/extrusion mechanism remains to be fully elucidated. To clarify Ca2+-transport in rat ameloblasts, we investigated expression and localization of N...

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Main Authors: Reijiro Okumura (Author), Yoshiyuki Shibukawa (Author), Takashi Muramatsu (Author), Sadamitsu Hashimoto (Author), Kan-Ichi Nakagawa (Author), Masakazu Tazaki (Author), Masaki Shimono (Author)
Format: Book
Published: Elsevier, 2010-01-01T00:00:00Z.
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Summary:Although the central role of ameloblasts in synthesis and resorption of enamel matrix proteins during amelogenesis is well documented, the Ca2+-transport/extrusion mechanism remains to be fully elucidated. To clarify Ca2+-transport in rat ameloblasts, we investigated expression and localization of Na+-Ca2+ exchanger (NCX) isoforms and the functional characteristics of their ion transporting/pharmacological properties. RT-PCR and immunohistochemical analyses revealed expression of NCX1 and NCX3 in ameloblasts, localized in the apical membrane. In patch-clamp recordings, Ca2+ efflux by Na+-Ca2+ exchange showed dependence on external Na+. Ca2+ influx by Na+-Ca2+ exchange, measured by fura-2 fluorescence, showed dependence on extracellular Ca2+ concentration, and it was blocked by NCX inhibitors KB-R7943, SEA0400, and SN-6. These results showed significant expression of NCX1 and NCX3 in ameloblasts, indicating their involvement in the directional Ca2+ extrusion pathway from cells to the enamel mineralizing front. Keywords:: transporter, enamel, mineralization, channel, SLC8 gene family
Item Description:1347-8613
10.1254/jphs.09267FP