| Literature DB >> 30963569 |
Yam Prasad Aryal1, Sanjiv Neupane1, Nirpesh Adhikari1, Chang-Hyeon An2, Jung-Hong Ha3, Tae-Yub Kwon4, Hitoshi Yamamoto5, Jae-Kwang Jung6, Eui-Kyun Park7, Ji-Youn Kim8, Sung-Won Cho9, Wern-Joo Sohn10, Youngkyun Lee1, Han-Jung Chae11, Hyung-Ryong Kim12, Jae-Young Kim1.
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.Entities:
Keywords: ER stress; Tmbim6 knockout; amelogenesis; dentinogenesis; molar development
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Year: 2019 PMID: 30963569 DOI: 10.1002/jcp.28635
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384