Department of Diagnostic & Biomedical Sciences, The University of Texas Health Science Center at Houston, School of Dentistry, Houston, TX, USA.
Center for Craniofacial Research, The University of Texas Health Science Center at Houston, School of Dentistry, Houston, TX, USA.
J Dent Res. 2023 Aug;102(9):1047-1057. doi: 10.1177/00220345231169220. Epub 2023 May 30.
Tooth enamel is generated by ameloblasts. Any failure in amelogenesis results in defects in the enamel, a condition known as amelogenesis imperfecta. Here, we report that mice with deficient autophagy in epithelial-derived tissues ( and conditional knockout mice) exhibit amelogenesis imperfecta. Micro-computed tomography imaging confirmed that enamel density and thickness were significantly reduced in the teeth of these mice. At the molecular level, ameloblast differentiation was compromised through ectopic accumulation and activation of NRF2, a specific substrate of autophagy. Through bioinformatic analyses, we identified , , , , , and as candidate genes related to amelogenesis imperfecta and the NRF2-mediated pathway. To investigate the effects of the ectopic NRF2 pathway activation caused by the autophagy deficiency, we analyzed target gene expression and NRF2 binding to the promoter region of candidate target genes and found suppressed gene expression of , , , and but not of and . Taken together, our findings indicate that autophagy plays a crucial role in ameloblast differentiation and that its failure results in amelogenesis imperfecta through ectopic NRF2 activation.
牙釉质是由成釉细胞产生的。成釉细胞生成过程中的任何失败都会导致釉质缺陷,这种情况被称为釉质发育不全。在这里,我们报告了上皮源性组织中自噬缺陷的小鼠( 和 条件性敲除小鼠)表现出釉质发育不全。微计算机断层扫描成像证实,这些小鼠的牙齿中釉质密度和厚度显著降低。在分子水平上,通过自噬的特定底物 NRF2 的异位积累和激活,成釉细胞分化受到损害。通过生物信息学分析,我们鉴定出 、 、 、 、 和 作为与釉质发育不全和 NRF2 介导的途径相关的候选基因。为了研究自噬缺陷引起的异位 NRF2 途径激活的影响,我们分析了候选靶基因的靶基因表达和 NRF2 与启动子区域的结合,发现 、 、 和 的基因表达受到抑制,但 和 不受抑制。总之,我们的研究结果表明,自噬在成釉细胞分化中起着至关重要的作用,其缺失通过异位 NRF2 激活导致釉质发育不全。