AGEs impair osteogenesis in orthodontic force-induced periodontal ligament stem cells through the KDM6B/Wnt self-reinforcing loop.

IF 7.1 2区 医学 Q1 CELL & TISSUE ENGINEERING Stem Cell Research & Therapy Pub Date : 2024-11-15 DOI:10.1186/s13287-024-04058-8
Qiaohui Ying, Yujun Jiang, Changyun Sun, Yaoguang Zhang, Ruihan Gao, Hongrui Liu, Hongrui Liu, Jie Guo, Minqi Li
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Abstract

Background: Diabetes, occasionally diagnosed in orthodontic patients, can impede orthodontic tooth movement (OTM) by accumulating advanced glycation end products (AGEs) in the periodontium. This accumulation impairs the osteogenic differentiation of periodontal ligament stem cells (PDLSCs) due to alterations in the force-loaded microenvironment, yet the underlying mechanisms remain elusive.

Methods: Bioinformatics analysis of GSE112122 identified alterations in the mechanical regulation of histone methylation enzyme Lysine Demethylase 6B (KDM6B). OTM models were established in healthy and Nicotinamide/ Streptozotocin-induced type II diabetic rats. The impact of AGEs on mechanically induced osteogenesis and its correlation with KDM6B were evaluated by assessing the therapeutic effects of periodontal ligament injections of the AGEs/RAGE inhibitor FPS-ZM1. To investigate transcriptomic changes, we extracted human PDLSCs, which were subjected to RNA sequencing following the overexpression of KDM6B. Experimental validation further identified potential self-reinforcing loops and their associated antioxidative mechanisms.

Results: Mechanical forces upregulated KDM6B expression and function in PDLSCs, modulating extensive downstream osteogenesis-related transcriptional changes. Experiments with AGEs-treated and FPS-ZM1-treated samples demonstrated that AGEs impaired osteogenesis by compromising KDM6B mechanical responsiveness. A positive feedback loop between KDM6B and Wnt pathways was identified, inhibited by AGEs. This loop regulated superoxide dismutase 2 (SOD2), facilitating antioxidative stress and preventing stem cell ageing.

Conclusions: This study elucidates a novel mechanism by which AGEs influence the osteogenic process and antioxidative capacity of PDLSCs through the KDM6B/Wnt self-reinforcing loop under orthodontic force. Targeting the AGE/RAGE pathway or enhancing KDM6B may enhance orthodontic treatments for diabetic patients.

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AGEs 通过 KDM6B/Wnt 自我强化环路损害正畸力诱导的牙周韧带干细胞的成骨作用。
背景:正畸患者偶尔会被诊断出患有糖尿病,糖尿病会通过在牙周积累高级糖化终产物(AGEs)而阻碍正畸牙齿移动(OTM)。由于受力微环境的改变,这种积累会损害牙周韧带干细胞(PDLSCs)的成骨分化,但其潜在机制仍然难以捉摸:GSE112122的生物信息学分析发现了组蛋白甲基化酶赖氨酸去甲基化酶6B(KDM6B)机械调控的改变。在健康大鼠和尼古丁酰胺/链脲佐菌素诱导的 II 型糖尿病大鼠中建立了 OTM 模型。通过评估牙周韧带注射 AGEs/RAGE 抑制剂 FPS-ZM1 的治疗效果,评估了 AGEs 对机械诱导成骨的影响及其与 KDM6B 的相关性。为了研究转录组的变化,我们提取了人类 PDLSCs,并在 KDM6B 过表达后对其进行了 RNA 测序。实验验证进一步确定了潜在的自我强化环路及其相关的抗氧化机制:结果:机械力上调了 KDM6B 在 PDLSCs 中的表达和功能,调节了广泛的下游成骨相关转录变化。用AGEs处理过的样本和FPS-ZM1处理过的样本进行的实验表明,AGEs会损害KDM6B的机械响应性,从而影响成骨过程。在 KDM6B 和 Wnt 通路之间发现了一个正反馈回路,AGEs 可抑制这一回路。这一环路调节超氧化物歧化酶2(SOD2),促进抗氧化压力,防止干细胞老化:本研究阐明了在正畸力作用下,AGE通过KDM6B/Wnt自我强化环路影响PDLSCs成骨过程和抗氧化能力的新机制。针对 AGE/RAGE 通路或增强 KDM6B 可提高糖尿病患者的正畸治疗效果。
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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
期刊最新文献
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