Department of Orthodontics, Applied Life Sciences, Hiroshima University Institute of Biomedical & Health Sciences, 1-2-3 Kasumi, Minami-ku, Hiroshima, Japan.
PLoS One. 2013;8(1):e54449. doi: 10.1371/journal.pone.0054449. Epub 2013 Jan 23.
Tooth root formation begins after the completion of crown morphogenesis. At the end edge of the tooth crown, inner and outer enamel epithelia form Hertwig's epithelial root sheath (HERS). HERS extends along with dental follicular tissue for root formation. Ameloblastin (AMBN) is an enamel matrix protein secreted by ameloblasts and HERS derived cells. A number of enamel proteins are eliminated in root formation, except for AMBN. AMBN may be related to tooth root formation; however, its role in this process remains unclear. In this study, we found AMBN in the basal portion of HERS of lower first molar in mice, but not at the tip. We designed and synthesized small interfering RNA (siRNA) targeting AMBN based on the mouse sequence. When AMBN siRNA was injected into a prospective mandibular first molar of postnatal day 10 mice, the root became shorter 10 days later. Furthermore, HERS in these mice revealed a multilayered appearance and 5-bromo-2'-deoxyuridine (BrdU) positive cells increased in the outer layers. In vitro experiments, when cells were compared with and without transiently expressing AMBN mRNA, expression of growth suppressor genes such as p21(Cip1) and p27(Kip1) was enhanced without AMBN and BrdU incorporation increased. Thus, AMBN may regulate differentiation state of HERS derived cells. Moreover, our results suggest that the expression of AMBN in HERS functions as a trigger for normal root formation.
牙根形成始于牙冠形态发生完成之后。在牙冠的末端边缘,内釉上皮和外釉上皮形成 Hertwig 上皮根鞘(HERS)。HERS 与牙囊组织一起延伸,以进行牙根形成。釉原蛋白(AMBN)是成釉细胞分泌的釉基质蛋白,也是 HERS 衍生细胞分泌的蛋白。在牙根形成过程中,除了 AMBN 之外,许多釉蛋白被消除。AMBN 可能与牙根形成有关,但它在这个过程中的作用尚不清楚。在这项研究中,我们在小鼠下第一磨牙的 HERS 的基底部发现了 AMBN,但在尖端没有发现。我们根据小鼠序列设计并合成了针对 AMBN 的小干扰 RNA(siRNA)。当 AMBN siRNA 被注射到出生后第 10 天的小鼠下颌第一磨牙的预期位置时,10 天后根变得更短。此外,这些小鼠的 HERS 呈现出多层外观,外层的 5-溴-2'-脱氧尿苷(BrdU)阳性细胞增加。在体外实验中,当比较有和没有瞬时表达 AMBN mRNA 的细胞时,在没有 AMBN 的情况下,生长抑制基因如 p21(Cip1)和 p27(Kip1)的表达增强,并且 BrdU 掺入增加。因此,AMBN 可能调节 HERS 衍生细胞的分化状态。此外,我们的结果表明,HERS 中 AMBN 的表达作为正常牙根形成的触发因素。