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血管生成素样蛋白4调节牙周膜干细胞的成骨分化。

ANGPTL4 regulates the osteogenic differentiation of periodontal ligament stem cells.

作者信息

Xu Lingli, Wang Chengze, Li Yongzheng, Wang Ying, Fu Baiping, Yang Guoli

机构信息

School of Stomatology, Zhejiang Provincial Clinical Research Center for Oral Diseases, Stomatology HospitalZhejiang University School of MedicineKey Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Hangzhou, 310006, China.

出版信息

Funct Integr Genomics. 2022 Oct;22(5):769-781. doi: 10.1007/s10142-022-00882-4. Epub 2022 Jul 13.

Abstract

The molecular mechanism of mechanical force regulating the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) has not been clearly elucidated. In this study, two mRNA-seqs, GSE106887 and GSE109167, which contained several samples of PDLSCs under mechanical force, were downloaded from Gene Expression Omnibus. Differential expression analysis was firstly taken between GSE106887 and GSE109167, then the common 84 up-regulated genes and 26 down-regulated genes were selected. Function enrichment analysis was used to identify the key genes and pathways in PDLSCs subjected to the tension and compression force. PDLSCs were isolated from human periodontal ligament tissues. The effects of ANGPTL4 knockdown with shRNA on the osteogenic differentiation of PDLSCs were studied in vitro. Then, the orthodontic tooth movement (OTM) rat model was used to study the expression of HIF-1α and ANGPTL4 in alveolar bone remodeling in vivo. ANGPTL4 and the HIF-1 pathway were identified in PDLSCs subjected to the tension and compression force. alizarin red staining, alcian blue staining, and oil red O staining verified that PDLSCs had the ability of osteogenic, chondrogenic, and adipogenic differentiation, respectively. Verification experiment revealed that the expression of ANGPTL4 in PDLSCs significantly increased when cultured under osteogenic medium in vitro. While ANGPTL4 was knocked down by shRNA, the levels of ALPL, RUNX2, and OCN decreased significantly, as well as the protein levels of COL1A1, ALPL, RUNX2, and OCN. During the OTM, the expression of HIF-1α and ANGPTL4 in periodontal ligament cells increased on the tension and compression sides. We concluded the positive relationship between ANGPTL4 and osteogenic differentiation of PDLSCs.

摘要

机械力调节牙周膜干细胞(PDLSCs)成骨分化的分子机制尚未完全阐明。在本研究中,从基因表达综合数据库下载了两个mRNA序列GSE106887和GSE109167,其中包含在机械力作用下的多个PDLSCs样本。首先对GSE106887和GSE109167进行差异表达分析,然后筛选出84个共同上调基因和26个共同下调基因。采用功能富集分析来鉴定承受拉伸和压缩力的PDLSCs中的关键基因和通路。从人牙周膜组织中分离出PDLSCs。在体外研究了用shRNA敲低ANGPTL4对PDLSCs成骨分化的影响。然后,使用正畸牙移动(OTM)大鼠模型研究体内牙槽骨重塑中HIF-1α和ANGPTL4的表达。在承受拉伸和压缩力的PDLSCs中鉴定出ANGPTL4和HIF-1通路。茜素红染色、阿尔辛蓝染色和油红O染色分别证实PDLSCs具有成骨、成软骨和成脂分化能力。验证实验表明,体外在成骨培养基中培养时,PDLSCs中ANGPTL4的表达显著增加。当用shRNA敲低ANGPTL4时,ALPL、RUNX2和OCN的水平显著降低,COL1A1、ALPL、RUNX2和OCN的蛋白水平也降低。在OTM过程中,牙周膜细胞中HIF-1α和ANGPTL4在拉伸侧和压缩侧的表达均增加。我们得出ANGPTL4与PDLSCs成骨分化之间呈正相关的结论。

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