Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Department of Oral and Maxillofacial Radiology, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
J Cell Physiol. 2019 Nov;234(11):20354-20365. doi: 10.1002/jcp.28635. Epub 2019 Apr 8.
To understand the role of endoplasmic reticulum (ER)-stress in mice molar development, we studied Tmbim6 that antagonizes the unfolded protein response, using Tmbim6 knockout (KO) mice and in vitro organ cultivation with knocking down using small interfering RNA. During molar development, Tmbim6 is expressed in developing tooth at E14-E16, postnatal0 (PN0), and PN6. Mineral content in Tmbim6 KO enamel was reduced while dentin was slightly increased revealing ultrastructural changes in pattern formation of both enamel and dentin. Moreover, odontoblast differentiation was altered with increased Dspp expression at PN0 followed by altered AMELX localizations at PN5. These results were confirmed by in vitro organ cultivation and showed altered Bmp signaling, proliferation, and actin rearrangement in the presumptive ameloblast and odontoblasts that followed the altered expression of differentiation and ER stress-related signaling molecules at E16.5. Overall, ER stress modulated by Tmbim6 would play important roles in patterned dental hard tissue formation in mice molar within a limited period of development.
为了研究内质网应激(ER-stress)在小鼠磨牙发育中的作用,我们使用 Tmbim6 敲除(KO)小鼠和使用小干扰 RNA(siRNA)敲低的体外器官培养,研究了拮抗未折叠蛋白反应的 Tmbim6。在磨牙发育过程中,Tmbim6 在 E14-E16、出生后 0 天(PN0)和 PN6 的发育牙齿中表达。Tmbim6 KO 釉质中的矿物质含量减少,而牙本质略有增加,显示出釉质和牙本质形态形成的超微结构变化。此外,牙本质细胞分化发生改变,PN0 时 Dspp 表达增加,随后 PN5 时 AMELX 定位改变。这些结果通过体外器官培养得到证实,并显示出在 E16.5 时,分化和 ER 应激相关信号分子的表达改变后,推测的成釉细胞和牙本质细胞中的 Bmp 信号、增殖和肌动蛋白重排发生改变。总体而言,Tmbim6 调节的 ER 应激在小鼠磨牙有限的发育时间内对有图案的牙齿硬组织形成起着重要作用。