Nagata Mizuki, Iwasaki Kengo, Akazawa Keiko, Komaki Motohiro, Yokoyama Naoki, Izumi Yuichi, Morita Ikuo
1 Department of Periodontology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University , Tokyo, Japan .
2 Department of Nanomedicine (DNP), Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University , Tokyo, Japan .
Tissue Eng Part A. 2017 May;23(9-10):367-377. doi: 10.1089/ten.TEA.2016.0274. Epub 2017 Jan 27.
Periodontal disease is one of the most common infectious diseases in adults and is characterized by the destruction of tooth-supporting tissues. Mesenchymal stem cells (MSCs) comprise the mesoderm-originating stem cell population, which has been studied and used for cell therapy. However, because of the lower rate of cell survival after MSC transplantation in various disease models, paracrine functions of MSCs have been receiving increased attention as a regenerative mechanism. The aim of this study was to investigate the regenerative potential of transplanted conditioned medium (CM) obtained from cultured periodontal ligament stem cells (PDLSCs), the adult stem cell population in tooth-supporting tissues, using a rat periodontal defect model. Cell-free CM was collected from PDLSCs and fibroblasts, using ultrafiltration and transplanted into surgically created periodontal defects. Protein content of CM was examined by antibody arrays. Formation of new periodontal tissues was analyzed using microcomputed tomography and histological sections. PDLSC-CM transplantation enhanced periodontal tissue regeneration in a concentration-dependent manner, whereas fibroblast-CM did not show any regenerative function. Proteomic analysis revealed that extracellular matrix proteins, enzymes, angiogenic factors, growth factors and cytokines were contained in PDLSC-CM. Furthermore, PDLSC-CM transplantation resulted in the decreased mRNA level of tumor necrosis factor-α (TNF-α) in healing periodontal tissues. In addition, we found that PDLSC-CM suppressed the mRNA level of TNF-α in the monocyte/macrophage cell line, RAW cells, stimulated with IFN-γ. Our findings suggested that PDLSC-CM enhanced periodontal regeneration by suppressing the inflammatory response through TNF-α production, and transplantation of PDLSC-CM could be a novel approach for periodontal regenerative therapy.
牙周病是成年人中最常见的传染病之一,其特征是牙齿支持组织遭到破坏。间充质干细胞(MSCs)是起源于中胚层的干细胞群体,已被研究并用于细胞治疗。然而,由于在各种疾病模型中间充质干细胞移植后细胞存活率较低,间充质干细胞的旁分泌功能作为一种再生机制受到了越来越多的关注。本研究的目的是使用大鼠牙周缺损模型,研究从培养的牙周膜干细胞(PDLSCs)(牙齿支持组织中的成体干细胞群体)获得的移植条件培养基(CM)的再生潜力。使用超滤从牙周膜干细胞和成纤维细胞中收集无细胞条件培养基,并将其移植到手术创建的牙周缺损中。通过抗体阵列检测条件培养基的蛋白质含量。使用微型计算机断层扫描和组织学切片分析新牙周组织的形成。牙周膜干细胞条件培养基移植以浓度依赖的方式增强了牙周组织再生,而成纤维细胞条件培养基未显示出任何再生功能。蛋白质组学分析表明,牙周膜干细胞条件培养基中含有细胞外基质蛋白、酶、血管生成因子、生长因子和细胞因子。此外,牙周膜干细胞条件培养基移植导致愈合中的牙周组织中肿瘤坏死因子-α(TNF-α)的mRNA水平降低。此外,我们发现牙周膜干细胞条件培养基抑制了用干扰素-γ刺激的单核细胞/巨噬细胞系RAW细胞中TNF-α的mRNA水平。我们的研究结果表明,牙周膜干细胞条件培养基通过抑制TNF-α产生的炎症反应来增强牙周再生,并且牙周膜干细胞条件培养基移植可能是牙周再生治疗的一种新方法。