Effects of ECM Components on Periodontal Ligament Stem Cell Differentiation Under Conditions of Disruption of Wnt and TGF-β Signaling Pathways.

IF 5 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Alla V Kuznetsova, Olga P Popova, Tamara I Danilova, Andrey V Latyshev, Oleg O Yanushevich, Alexey A Ivanov
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Abstract

Periodontitis is accompanied by inflammation that causes dysregulation of the Wnt/β-catenin and TGF-β signaling pathways. This leads to a violation of the homeostasis of periodontal tissues. Components of the extracellular matrix (ECM) are an important part of biomaterials used for the repair of periodontal tissue. The purpose of this study was to evaluate the components of the effect of ECM (hyaluronic acid (HA), fibronectin (Fn), and laminin (Lam)) on the osteogenic and odontogenic differentiation of periodontal ligament stem cells (PDLSCs) in the collagen I hydrogel under conditions of disruption of the Wnt/β-catenin and TGF-β signaling pathways. The study showed that the addition of components of the ECM restored the expression of odontogenic markers in PDLSCs, which was absent during inhibition of the canonical Wnt signaling pathway, and their multidirectional effect on the secretion of transforming growth factor-β1 (TGF-β1) and bone morphogenetic protein 2 (BMP-2). Fn and Lam suppressed the expression of odontogenic markers in PDLSCs against the background of inhibition of the TGF-β signaling pathway. The addition of HA under the conditions of the TGF-β signaling pathway improved BMP-2 secretion, preserving odontogenic differentiation. Thus, our results demonstrated that disruption of the Wnt/β-catenin and TGF-β signaling pathways causes disorders in the differentiation of PDLSCs, preventing the regeneration of periodontal tissues. This should be taken into account when developing multicomponent scaffolds that recapitulate the ECM microenvironment at endogenic regeneration of the periodontium. Inclusion of hyaluronic acid as one of these components may enhance the therapeutic effect of such biomaterials.

在Wnt和TGF-β信号通路中断的情况下,ECM成分对牙周韧带干细胞分化的影响。
牙周炎伴有炎症,导致Wnt/β-catenin和TGF-β信号通路失调。这就会破坏牙周组织的体内平衡。细胞外基质(ECM)成分是修复牙周组织的生物材料的重要组成部分。本研究的目的是在Wnt/β-catenin和TGF-β信号通路被破坏的情况下,评估ECM(透明质酸(HA)、纤维连接蛋白(Fn)和层粘连蛋白(Lam))在I型胶原水凝胶中对牙周韧带干细胞(PDLSCs)成骨和成牙分化的影响。本研究表明,加入ECM组分后,PDLSCs中牙源性标志物的表达得以恢复,而这些标志物在抑制典型Wnt信号通路时是缺失的,它们对转化生长因子-β1 (TGF-β1)和骨形态发生蛋白2 (BMP-2)的分泌具有多向作用。Fn和Lam通过抑制TGF-β信号通路抑制PDLSCs中牙源性标志物的表达。在TGF-β信号通路条件下,添加HA可改善BMP-2分泌,保持牙源性分化。因此,我们的研究结果表明,Wnt/β-catenin和TGF-β信号通路的破坏导致PDLSCs分化障碍,阻止牙周组织的再生。在开发多组分支架时应考虑到这一点,这些支架在牙周组织的内源性再生中再现了ECM微环境。包含透明质酸作为这些成分之一可以增强这种生物材料的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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