Kwak Seo-Young, Green Samantha, Wiedemann-Bidlack Felicitas B, Beniash Elia, Yamakoshi Yasuo, Simmer James P, Margolis Henry C
Department of Biomineralization, The Forsyth Institute, Cambridge, MA 02142, USA.
Eur J Oral Sci. 2011 Dec;119 Suppl 1(Suppl 1):103-11. doi: 10.1111/j.1600-0722.2011.00911.x.
Amelogenin is essential for proper enamel formation. The present in vitro study extends our previous work at low (10 mM) ionic strength (IS) by examining the effect of amelogenin on mineralization under higher (162 mM) IS conditions found in developing enamel. Full-length phosphorylated (P173) and non-phosphorylated (rP172) amelogenins were examined, along with P148 and rP147 that lack the hydrophilic C-terminus. Calcium phosphate formation was assessed by pH change, while the minerals formed were characterized using transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy. Amelogenin self-assembly was also studied using dynamic light scattering and TEM. The results indicate that IS does not influence the effects of rP147, rP172, and P173 on mineralization. However, in contrast to the findings for low IS, where both P173 and P148 stabilize initially formed amorphous calcium phosphate (ACP) nanoparticles for >1 d, elongated hydroxyapatite crystals were observed after 24 h using P148 at high IS, unlike that seen with P173. Differences in self-assembly help explain these findings, which suggest that P173 and P148 may play different roles in regulating enamel mineral formation. The present data support the notion that proteolytic processing of P173 is required in vivo to induce the transformation of initial ACP phases to apatitic enamel crystals.
釉原蛋白对于正常牙釉质形成至关重要。本体外研究扩展了我们之前在低离子强度(10 mM)条件下的工作,通过研究釉原蛋白在发育中的牙釉质中较高离子强度(162 mM)条件下对矿化的影响。研究了全长磷酸化(P173)和非磷酸化(rP172)釉原蛋白,以及缺乏亲水性C末端的P148和rP147。通过pH变化评估磷酸钙的形成,同时使用透射电子显微镜(TEM)和傅里叶变换红外光谱对形成的矿物质进行表征。还使用动态光散射和TEM研究了釉原蛋白的自组装。结果表明,离子强度不影响rP147、rP172和P173对矿化的作用。然而,与低离子强度下的研究结果不同,在低离子强度下P173和P148都能使最初形成的无定形磷酸钙(ACP)纳米颗粒稳定超过1天,而在高离子强度下使用P148时,24小时后观察到了细长的羟基磷灰石晶体,这与P173不同。自组装的差异有助于解释这些发现,这表明P173和P148在调节牙釉质矿化形成中可能发挥不同作用。目前的数据支持这样一种观点,即体内需要对P173进行蛋白水解加工,以诱导初始ACP相转变为磷灰石牙釉质晶体。