Department of Pediatric Dentistry, School and Hospital of Stomatology, Peking University, Beijing, China.
Department of Pediatric Dentistry, School and Hospital of Stomatology, Peking University, Beijing, China.
Arch Oral Biol. 2022 Sep;141:105492. doi: 10.1016/j.archoralbio.2022.105492. Epub 2022 Jun 22.
In the present study, we aimed to investigate whether long non-coding RNA (lncRNA) insulin-like growth factor binding protein 7-antisense 1 (IGFBP7-AS1) regulates the odonto-differentiation of stem cells from human exfoliated deciduous teeth (SHED) and its underlying mechanism.
Real-time polymerase chain reaction (PCR) and correlation analysis were used to determine the expression of IGFBP7-AS1 during odontogenesis. Alkaline phosphate staining, alizarin red S staining, and real-time PCR in vitro were performed to investigate the effects of IGFBP7-AS1 during odontogenesis. Western blot and immunostaining (with or without chloroquine treatment) were applied to detect the expression of the autophagy-related markers, microtubule-associated proteins 1A/1B light chain 3B (LC3B) and p62. The autophagy inhibitor 3-methyladenine was used to further clarify the effect of autophagy in odonto-differentiation as promoted by IGFBP7-AS1.
The expression of lncRNA IGFBP7-AS1 is significantly upregulated during odonto-differentiation of SHED and promotes odontogenesis of SHED in vitro. IGFBP7-AS1 promotes autophagy during odontogenesis.
IGFBP7-AS1 elicits odontogenic differentiation of SHED through autophagy. Furthermore, IGFBP7-AS1 shows promise as a gene target in the regeneration of dental hard tissue and dental-pulp complex.
本研究旨在探讨长链非编码 RNA(lncRNA)胰岛素样生长因子结合蛋白 7 反义 1(IGFBP7-AS1)是否调节人乳牙脱落干细胞(SHED)的牙向分化及其潜在机制。
实时聚合酶链反应(PCR)和相关分析用于确定 IGFBP7-AS1 在牙发生过程中的表达。体外碱性磷酸酶染色、茜素红 S 染色和实时 PCR 用于研究 IGFBP7-AS1 在牙发生过程中的作用。Western blot 和免疫染色(有或没有氯喹处理)用于检测自噬相关标志物微管相关蛋白 1A/1B 轻链 3B(LC3B)和 p62 的表达。自噬抑制剂 3-甲基腺嘌呤用于进一步阐明 IGFBP7-AS1 促进牙向分化过程中自噬的作用。
lncRNA IGFBP7-AS1 在 SHED 的牙向分化过程中表达显著上调,并在体外促进 SHED 的牙发生。IGFBP7-AS1 促进牙发生过程中的自噬。
IGFBP7-AS1 通过自噬引发 SHED 的牙向分化。此外,IGFBP7-AS1 有望成为牙硬组织和牙髓复合体再生的基因靶点。