成牙本质细胞
内质网
成釉细胞
牙本质
未折叠蛋白反应
细胞生物学
臼齿
釉原蛋白
搪瓷漆
釉质形成
生物
化学
生物化学
基因
牙科
医学
古生物学
作者
Yam Prasad Aryal,Sanjiv Neupane,Nirpesh Adhikari,Chang‐Hyeon An,Jung‐Hong Ha,Tae‐Yub Kwon,Hitoshi Yamamoto,Jae‐Kwang Jung,Eui Kyun Park,Ji‐Youn Kim,Sung Won Cho,Wern‐Joo Sohn,Youngkyun Lee,Han‐Jung Chae,Hyung‐Ryong Kim,Jae‐Young Kim
摘要
Abstract 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.
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