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KLF2通过调控Nrf2表达促进人牙周膜干细胞的成骨分化。

KLF2 Promotes Osteogenic Differentiation of Human Periodontal Ligament Stem Cells by Regulating Nrf2 Expression.

作者信息

Chen Jiujiu, Deng Lichao

机构信息

Pediatric Dentistry, Wenzhou Dental Hospital, Wenzhou, Zhejiang, China.

Endodontic Department, School & Hospital of Stomatology Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Int Dent J. 2025 Jun;75(3):1554-1563. doi: 10.1016/j.identj.2025.02.019. Epub 2025 Mar 22.

Abstract

OBJECTIVE

Periodontal ligament stem cells (PDLSCs) are emerging as a promising source for periodontal regeneration and to manage periodontitis. This study aims to investigate the roles of Krüppel-like factor 2 (KLF2) and nuclear factor erythroid 2-related factor (Nrf2) in mediating osteogenic differentiation of human PDLSCs (hPDLSCs) in the context of lipopolysaccharide (LPS) stimulation.

METHODS

The osteogenic differentiation potential of hPDLSCs isolated from human premolar root samples were examined by alkaline phosphatase (ALP) staining and ALP activity assay, Alizarin red S staining and quantitative analysis of mineralised matrix. Intracellular reactive oxygen species (ROS) production and glutathione (GSH) concentration were assessed to reflect oxidative stress.

RESULTS

KLF2 overexpression influenced Nrf2-regulated transcription, leading to significant increases in GSH concentration, ALP activity, mineralised matrix formation, and RUNX2 expression in LPS-stimulated hPDLSCs, as well as significant reductions in ROS production and cell apoptosis. The subsequent Nrf2 knockdown impaired the protective effect of KLF2 on hPDLSCs against LPS stimulation.

CONCLUSION

The findings of the study demonstrate KLF2 overexpression has the ability to promote the osteogenic differentiation of hPDLSCs by promoting Nrf2 activation, suggesting that KLF2 mediating Nrf2 could be a promising target to facilitate the efficacy of PDLSC-based bone regeneration in periodontitis.

摘要

目的

牙周膜干细胞(PDLSCs)正成为牙周组织再生和治疗牙周炎的一种有前景的细胞来源。本研究旨在探讨Krüppel样因子2(KLF2)和核因子红细胞2相关因子(Nrf2)在脂多糖(LPS)刺激条件下介导人牙周膜干细胞(hPDLSCs)成骨分化中的作用。

方法

通过碱性磷酸酶(ALP)染色和ALP活性测定、茜素红S染色以及矿化基质的定量分析,检测从人前磨牙牙根样本中分离出的hPDLSCs的成骨分化潜能。评估细胞内活性氧(ROS)的产生和谷胱甘肽(GSH)浓度以反映氧化应激。

结果

KLF2过表达影响Nrf2调控的转录,导致LPS刺激的hPDLSCs中GSH浓度、ALP活性、矿化基质形成和RUNX2表达显著增加,同时ROS产生和细胞凋亡显著减少。随后的Nrf2基因敲低削弱了KLF2对hPDLSCs抵抗LPS刺激的保护作用。

结论

该研究结果表明,KLF2过表达能够通过促进Nrf2激活来促进hPDLSCs的成骨分化,这表明KLF2介导Nrf2可能是提高基于PDLSCs的牙周炎骨再生疗效的一个有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe4d/11979923/e860c67a58b1/gr1.jpg

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