Forkhead Box O1 Promotes Osteogenic Differentiation of Periodontal Ligament Stem Cells in Hypoxia/Reoxygenation Environments by Regulating Heme Oxygenase-1 Scavenging of Reactive Oxygen Species

IF 3.2 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Yujia Ye , Jinqiao Tang , Jiahui Ye , Bin Zhao , Yanning Ma
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引用次数: 0

Abstract

Introduction and aims

Oral health is closely linked to systemic health, and patients with obstructive sleep apnea suffer from an increased risk of periodontitis due to repeated cycles of hypoxia/reoxygenation (H/R). This study aimed to assess the role of forkhead box O1 (FoxO1) in alveolar bone remodelling and explore how it affects H/R in vitro.

Methods

The AnaeroPack system was employed to establish an H/R model based on periodontal ligament stem cells (PDLSCs). Using alkaline phosphatase (ALP) staining, ALP activity test, alizarin red staining, and RT-qPCR, the osteogenic differentiation capacity of PDLSCs was detected under the H/R environment. The expression of FoxO1 was specifically knocked down and overexpressed using small interfering RNA and lentiviral transfection to investigate the role of FoxO1 in the osteogenic differentiation of PDLSCs and explore the underlying mechanism.

Results

H/R downregulated osteogenic indicators (collagen-I, RunX2, and ALP) in hPDLSCs (P < .01). In addition, the osteogenic capacity was found to be associated with the degree of H/R injury. FoxO1 positively regulated the osteogenic differentiation of PDLSCs (P < .01), and FoxO1 overexpression restored the osteogenic capacity of PDLSCs after H/R injury (P < .01). Further studies revealed that the heme oxygenase-1 signalling pathway was involved in FoxO1-mediated osteogenesis in PDLSCs.

Conclusion

In H/R, PDLSCs exhibited proliferative capacity and impaired osteogenic differentiation, which could be reversed by FoxO1 overexpression. Mechanistically, FoxO1 removed reactive oxygen species by regulating the expression of heme oxygenase-1, thereby enhancing the osteogenic differentiation of PDLSCs.

Clinical relevance

Given the positive effect of FoxO1 in alveolar bone remodelling in H/R, it could serve as a potential target for the treatment of periodontitis in patients with obstructive sleep apnea.
叉头盒O1通过调节血红素氧化酶-1清除活性氧促进缺氧/再氧化环境下牙周韧带干细胞的成骨分化
口腔健康与全身健康密切相关,阻塞性睡眠呼吸暂停患者由于缺氧/再氧合(H/R)的反复循环,患牙周炎的风险增加。本研究旨在评估叉头盒O1 (FoxO1)在牙槽骨重塑中的作用,并探讨其对体外H/R的影响。方法采用AnaeroPack系统建立牙周韧带干细胞(PDLSCs) H/R模型。采用碱性磷酸酶(ALP)染色、ALP活性测定、茜素红染色、RT-qPCR检测H/R环境下PDLSCs的成骨分化能力。利用小干扰RNA和慢病毒转染特异性敲除FoxO1的表达并过表达,研究FoxO1在PDLSCs成骨分化中的作用并探讨其潜在机制。结果sh /R下调hPDLSCs成骨指标(collagen-I、RunX2、ALP) (P <;. 01)。此外,发现成骨能力与H/R损伤程度有关。fox01正调控PDLSCs成骨分化(P <;.01), FoxO1过表达恢复了H/R损伤后PDLSCs的成骨能力(P <;. 01)。进一步研究发现,血红素加氧酶-1信号通路参与了fox01介导的PDLSCs成骨过程。结论在H/R条件下,PDLSCs表现出增殖能力和成骨分化能力受损,FoxO1过表达可逆转这一过程。机制上,FoxO1通过调节血红素加氧酶-1的表达去除活性氧,从而促进PDLSCs的成骨分化。鉴于FoxO1在H/R牙槽骨重塑中的积极作用,它可能作为治疗阻塞性睡眠呼吸暂停患者牙周炎的潜在靶点。
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来源期刊
International dental journal
International dental journal 医学-牙科与口腔外科
CiteScore
4.80
自引率
6.10%
发文量
159
审稿时长
63 days
期刊介绍: The International Dental Journal features peer-reviewed, scientific articles relevant to international oral health issues, as well as practical, informative articles aimed at clinicians.
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