Takewaki M, Kajiya M, Takeda K, Sasaki S, Motoike S, Komatsu N, Matsuda S, Ouhara K, Mizuno N, Fujita T, Kurihara H
1 Department of Periodontal Medicine, Applied Life Sciences, Institute of Biomedical & Health Sciences, Graduate School of Biomedical & Health Sciences, Hiroshima University, Minami-ku, Hiroshima, Japan.
J Dent Res. 2017 Aug;96(9):984-991. doi: 10.1177/0022034517708770. Epub 2017 May 18.
Transplantation of mesenchymal stem cells (MSCs), which possess self-renewing properties and multipotency, into a periodontal defect is thought to be a useful option for periodontal tissue regeneration. However, developing more reliable and predictable implantation techniques is still needed. Recently, we generated clumps of an MSC/extracellular matrix (ECM) complex (C-MSC), which consisted of cells and self-produced ECM. C-MSCs can regulate their cellular functions in vitro and can be grafted into a defect site, without any artificial scaffold, to induce bone regeneration. Accordingly, this study aimed to evaluate the effect of C-MSC transplantation on periodontal tissue regeneration in beagle dogs. Seven beagle dogs were employed to generate a premolar class III furcation defect model. MSCs isolated from dog ilium were seeded at a density of 7.0 × 10 cells/well into 24-well plates and cultured in growth medium supplemented with 50 µg/mL ascorbic acid for 4 d. To obtain C-MSCs, confluent cells were scratched using a micropipette tip and were then torn off as a cellular sheet. The sheet was rolled up to make round clumps of cells. C-MSCs were maintained in growth medium or osteoinductive medium (OIM) for 5 or 10 d. The biological properties of C-MSCs were evaluated in vitro, and their periodontal tissue regenerative activity was tested by using a dog class III furcation defect model. Immunofluorescence analysis revealed that type I collagen fabricated the form of C-MSCs. OIM markedly elevated calcium deposition in C-MSCs at day 10, suggesting its osteogenic differentiation capacity. Both C-MSCs and C-MSCs cultured with OIM transplantation without an artificial scaffold into the dog furcation defect induced periodontal tissue regeneration successfully compared with no graft, whereas osteogenic-differentiated C-MSCs led to rapid alveolar bone regeneration. These findings suggested that the use of C-MSCs refined by self-produced ECM may represent a novel predictable periodontal tissue regenerative therapy.
间充质干细胞(MSCs)具有自我更新特性和多能性,将其移植到牙周缺损处被认为是牙周组织再生的一种有效选择。然而,仍需要开发更可靠、可预测的植入技术。最近,我们制备了MSCs/细胞外基质(ECM)复合物团块(C-MSCs),其由细胞和自身产生的ECM组成。C-MSCs能够在体外调节其细胞功能,并且无需任何人工支架即可移植到缺损部位以诱导骨再生。因此,本研究旨在评估C-MSCs移植对比格犬牙周组织再生的影响。选用7只比格犬建立前磨牙III度根分叉缺损模型。从犬髂骨分离的MSCs以7.0×10个细胞/孔的密度接种到24孔板中,并在添加50μg/mL抗坏血酸的生长培养基中培养4天。为了获得C-MSCs,用微量移液器吸头刮擦汇合的细胞,然后将其撕成细胞片。将该片卷起制成圆形细胞团块。C-MSCs在生长培养基或骨诱导培养基(OIM)中维持培养5天或10天。在体外评估C-MSCs的生物学特性,并使用犬III度根分叉缺损模型测试其牙周组织再生活性。免疫荧光分析显示I型胶原构成了C-MSCs的形态。在第10天,OIM显著提高了C-MSCs中的钙沉积,表明其成骨分化能力。与未移植相比,C-MSCs和用OIM培养的C-MSCs在无人工支架的情况下移植到犬根分叉缺损处均成功诱导了牙周组织再生,而成骨分化的C-MSCs导致牙槽骨快速再生。这些发现表明使用由自身产生的ECM优化的C-MSCs可能代表一种新型的可预测的牙周组织再生疗法。