Nowwarote Nunthawan, Osathanon Thanaphum, Kanjana Kiattipan, Theerapanon Thanakorn, Porntaveetus Thantrira, Shotelersuk Vorasuk
Genomics and Precision Dentistry Research Unit, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.
Center of Excellence for Regenerative Dentistry, Department of Anatomy, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.
Genes Dis. 2019 Jul 29;6(4):391-397. doi: 10.1016/j.gendis.2019.07.005. eCollection 2019 Dec.
mutations lead to autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI). However, the biological role of remains unclear. The present study aimed to characterize the alveolar bone cells isolated from a patient with ADHCAI having the mutation, c.1261G > T, p.E421*, in . We showed that mutant cells had proliferation ability and morphology similar to the controls. The F-actin staining revealed that mutant cells were remained in the earlier stages of cell spreading compared to the controls at 30 min, but their spreading was advanced comparable to the controls at later stages. After osteogenic induction, a significant decrease in mRNA levels of and was observed in mutant cells at day 7 compared with day 3 while their expressions were increased in the controls. The levels in mutant cells were not significantly changed at day 7 compared to day 3 while the controls showed a significant increase. After 14 days, the mineral deposition of mutant cells was slightly lower than that of the controls. In conclusion, we identify that bone cells have lower expression of osteogenic marker genes and mineralization while they maintain their morphology, proliferation, and spreading. Consistent with previous studies in the ameloblasts and periodontal ligamental cells, these evidences propose that influences osteogenic differentiation across different cell types in oral cavity.
突变导致常染色体显性低钙化型牙釉质发育不全(ADHCAI)。然而,其生物学作用仍不清楚。本研究旨在对从一名患有ADHCAI且在[基因名称]中有c.1261G>T、p.E421*突变的患者分离出的牙槽骨细胞进行特征描述。我们发现[基因名称]突变细胞具有与对照相似的增殖能力和形态。F-肌动蛋白染色显示,在30分钟时,与对照相比,[基因名称]突变细胞仍处于细胞铺展的早期阶段,但在后期其铺展程度与对照相当。成骨诱导后,与第3天相比,在第7天观察到[基因名称]突变细胞中[相关基因名称1]和[相关基因名称2]的mRNA水平显著下降,而在对照中其表达增加。与第3天相比,[基因名称]突变细胞在第7天的[相关蛋白名称]水平没有显著变化,而对照显示出显著增加。14天后,[基因名称]突变细胞的矿物质沉积略低于对照。总之,我们发现[基因名称]骨细胞在保持其形态、增殖和铺展的同时,成骨标记基因的表达和矿化作用较低。与之前在成釉细胞和牙周韧带细胞中的研究一致,这些证据表明[基因名称]影响口腔中不同细胞类型的成骨分化。