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HOXA10通过调节β-连环蛋白定位和DKK1表达来抑制牙周膜干细胞的成骨分化。

HOXA10 inhibit the osteogenic differentiation of periodontal ligament stem cells by regulating β-catenin localization and DKK1 expression.

作者信息

Wang Chengze, Li Yongzheng, Yu Ke, Jiang Zhiwei, Wang Ying, Yang Guoli

机构信息

The Affiliated Stomatology Hospital, Zhejiang University, School of Medicine, Hangzhou, China.

Key Laboratory of Oral Biomedical Research of Zhejiang Province, Zhejiang University School of Stomatology, Hangzhou, China.

出版信息

Connect Tissue Res. 2021 Jul;62(4):393-401. doi: 10.1080/03008207.2020.1756271. Epub 2020 Apr 27.

Abstract

: Human periodontal ligament stem cells (hPDLSCs) are stem cells found near the tooth periodontal ligament. These cels are involved in the regeneration of the periodontal ligament and alveolar bone during orthodontic treatment and chronic periodontitis.: The Homeobox gene HOXA10 regulates the osteogenic differentiation of stem cells. However, the role of HOXA10 in hPDLSCs remains unclear. Therefore, we studied the effects of HOXA10 on human PDLSC osteogenic differentiation .: First, hPDLSCs were isolated and characterized. Second, we assessed the effects of overexpression and knockdown of HOXA10 on PDLSC osteogenic differentiation. Finally, the specific Wnt signaling pathway activator lithium chloride (LiCl) and inhibitor ICG-001 were used to investigate the involvement of the Wnt signaling pathway in HOXA10-induced regulation of osteogenic differentiation.: Overexpressing HOXA10 inhibited PDLSC osteogenic differentiation , shown by ALP and Alizarin Red staining, while HOXA10 knockdown demonstrated the opposite effects. HOXA10 negatively regulated nuclear β-catenin and osteogenic differentiation markers including alkaline phosphatase () and integrin-binding sialoprotein (). Upregulating HOXA10 reduced nuclear β-catenin and increased DKK1 expression. However, HOXA10 knockdown enhanced nuclear β-catenin accumulation and reduced DKK1 expression. These negative effects on osteogenic differentiation by HOXA10 overexpression were restored by the Wnt/β-catenin pathway activator LiCl. The increased osteogenic differentiation effects of HOXA10 knockdown were antagonized by ICG-001, a Wnt pathway inhibitor.: These data demonstrate that HOXA10 inhibits the osteogenic differentiation of periodontal ligament stem cells by regulating β-catenin localization and DKK1.

摘要

人牙周膜干细胞(hPDLSCs)是在牙齿牙周膜附近发现的干细胞。这些细胞在正畸治疗和慢性牙周炎期间参与牙周膜和牙槽骨的再生。

同源盒基因HOXA10调节干细胞的成骨分化。然而,HOXA10在hPDLSCs中的作用仍不清楚。因此,我们研究了HOXA10对人牙周膜干细胞成骨分化的影响。

首先,分离并鉴定hPDLSCs。其次,我们评估了HOXA10过表达和敲低对牙周膜干细胞成骨分化的影响。最后,使用特定的Wnt信号通路激活剂氯化锂(LiCl)和抑制剂ICG - 001来研究Wnt信号通路在HOXA10诱导的成骨分化调节中的作用。

HOXA10过表达抑制了牙周膜干细胞的成骨分化,碱性磷酸酶和茜素红染色显示了这一点,而HOXA10敲低则表现出相反的效果。HOXA10负向调节核β-连环蛋白和成骨分化标志物,包括碱性磷酸酶()和整合素结合涎蛋白()。上调HOXA10降低了核β-连环蛋白并增加了DKK1表达。然而,HOXA10敲低增强了核β-连环蛋白的积累并降低了DKK1表达。HOXA10过表达对成骨分化的这些负面影响通过Wnt/β-连环蛋白通路激活剂LiCl得以恢复。HOXA10敲低增加的成骨分化作用被Wnt通路抑制剂ICG - 001所拮抗。

这些数据表明,HOXA10通过调节β-连环蛋白定位和DKK1来抑制牙周膜干细胞的成骨分化。

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