Yun Hyung-Mun, Lee Eui-Suk, Kim Mi-joo, Kim Jung-Ju, Lee Jung-Hwan, Lee Hae-Hyoung, Park Kyung-Ran, Yi Jin-Kyu, Kim Hae-Won, Kim Eun-cheol
Department of Oral and Maxillofacial Pathology & Research Center for tooth and periodontal tissue regeneration (MRC), School of Dentistry, Kyung Hee University, Seoul, Korea.
Department of Oral and Maxillofacial Surgery, Guro Hospital, Korea University, Seoul, Republic of Korea.
PLoS One. 2015 Sep 18;10(9):e0138614. doi: 10.1371/journal.pone.0138614. eCollection 2015.
Magnetism is an intriguing physical cue that can alter the behaviors of a broad range of cells. Nanocomposite scaffolds that exhibit magnetic properties are thus considered useful 3D matrix for culture of cells and their fate control in repair and regeneration processes. Here we produced magnetic nanocomposite scaffolds made of magnetite nanoparticles (MNPs) and polycaprolactone (PCL), and the effects of the scaffolds on the adhesion, growth, migration and odontogenic differentiation of human dental pulp cells (HDPCs) were investigated. Furthermore, the associated signaling pathways were examined in order to elucidate the molecular mechanisms in the cellular events. The magnetic scaffolds incorporated with MNPs at varying concentrations (up to 10%wt) supported cellular adhesion and multiplication over 2 weeks, showing good viability. The cellular constructs in the nanocomposite scaffolds played significant roles in the stimulation of adhesion, migration and odontogenesis of HDPCs. Cells were shown to adhere to substantially higher number when affected by the magnetic scaffolds. Cell migration tested by in vitro wound closure model was significantly enhanced by the magnetic scaffolds. Furthermore, odontogenic differentiation of HDPCs, as assessed by the alkaline phosphatase activity, mRNA expressions of odontogenic markers (DMP-1, DSPP,osteocalcin, and ostepontin), and alizarin red staining, was significantly stimulated by the magnetic scaffolds. Signal transduction was analyzed by RT-PCR, Western blotting, and confocal microscopy. The magnetic scaffolds upregulated the integrin subunits (α1, α2, β1 and β3) and activated downstream pathways, such as FAK, paxillin, p38, ERK MAPK, and NF-κB. The current study reports for the first time the significant impact of magnetic scaffolds in stimulating HDPC behaviors, including cell migration and odontogenesis, implying the potential usefulness of the magnetic scaffolds for dentin-pulp tissue engineering.
磁性是一种有趣的物理信号,能够改变多种细胞的行为。因此,具有磁性的纳米复合支架被认为是用于细胞培养及其在修复和再生过程中命运控制的有用三维基质。在此,我们制备了由磁铁矿纳米颗粒(MNP)和聚己内酯(PCL)制成的磁性纳米复合支架,并研究了该支架对人牙髓细胞(HDPC)的黏附、生长、迁移和牙源性分化的影响。此外,还检测了相关信号通路,以阐明细胞事件中的分子机制。掺入不同浓度(高达10%重量)MNP的磁性支架在两周内支持细胞黏附和增殖,显示出良好的活力。纳米复合支架中的细胞构建体在刺激HDPC的黏附、迁移和牙源性分化中发挥了重要作用。当受到磁性支架影响时,细胞黏附数量显著增加。通过体外伤口闭合模型测试,磁性支架显著增强了细胞迁移。此外,通过碱性磷酸酶活性、牙源性标志物(DMP-1、DSPP、骨钙素和骨桥蛋白)的mRNA表达以及茜素红染色评估,磁性支架显著刺激了HDPC的牙源性分化。通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和共聚焦显微镜分析信号转导。磁性支架上调整合素亚基(α1、α2、β1和β3)并激活下游通路,如黏着斑激酶(FAK)、桩蛋白、p38、细胞外信号调节激酶丝裂原活化蛋白激酶(ERK MAPK)和核因子κB(NF-κB)。本研究首次报道了磁性支架在刺激HDPC行为(包括细胞迁移和牙源性分化)方面的显著影响,这意味着磁性支架在牙本质-牙髓组织工程中具有潜在的应用价值。