Inanç Bülend, Elçin A Eser, Unsal Evrim, Balos Köksal, Parlar Ates, Elçin Y Murat
Tissue Engineering and Biomaterials Laboratory, Department of Chemistry (Biochemistry), Faculty of Science and Biotechnology Institute, Ankara University, Ankara, Turkey.
Artif Organs. 2008 Feb;32(2):100-9. doi: 10.1111/j.1525-1594.2007.00499.x. Epub 2007 Nov 14.
Human embryonic stem cells (hESCs) are pluripotent cells with unlimited proliferation potential and differentiation capacity to all types of somatic cells. Periodontal tissue engineering based on in vitro expanded cells holds the promise to overcome the limitations associated with contemporary regenerative techniques. The aim of this study was to investigate the differentiation patterns of hESCs under the influence of periodontal ligament cells in vitro. hESCs (HUES-9) were expanded and characterized for their pluripotency. Then they were transfected with green fluorescent protein-carrying plasmid, and cocultured with human periodontal ligament fibroblastic cells for 21 days. Two experimental groups were established with different medium constituents. Specimens were fixed at days 7, 14, and 21 and were analyzed morphologically under inverted light microscope, and by immunohistochemistry using antibodies against collagen types I and III, fibronectin, fibroblast surface protein, vimentin, and pancytokeratin. Our results demonstrate different patterns of cell differentiation between groups, with about one-fifth of cells in colonies acquiring characteristics similar to periodontal ligament fibroblastic progenitors while others proceed toward distinctive lineages. This indicates the feasibility to direct the differentiation of hESCs toward the periodontal ligament fibroblastic progenitors to some extent. These findings support the notion that hESCs may become a cell source with unlimited supply for periodontal tissue engineering applications.
人胚胎干细胞(hESCs)是具有无限增殖潜能和向所有类型体细胞分化能力的多能细胞。基于体外扩增细胞的牙周组织工程有望克服当代再生技术的局限性。本研究的目的是在体外研究牙周膜细胞影响下人胚胎干细胞的分化模式。将人胚胎干细胞(HUES-9)进行扩增并鉴定其多能性。然后用携带绿色荧光蛋白的质粒转染它们,并与人牙周膜成纤维细胞共培养21天。建立了两个具有不同培养基成分的实验组。在第7天、14天和21天对标本进行固定,并在倒置光学显微镜下进行形态学分析,以及使用抗I型和III型胶原、纤连蛋白、成纤维细胞表面蛋白、波形蛋白和全细胞角蛋白的抗体进行免疫组织化学分析。我们的结果表明不同组之间存在不同的细胞分化模式,集落中约五分之一的细胞获得了类似于牙周膜成纤维细胞祖细胞的特征,而其他细胞则朝着不同的谱系发展。这表明在一定程度上引导人胚胎干细胞向牙周膜成纤维细胞祖细胞分化是可行的。这些发现支持了人胚胎干细胞可能成为牙周组织工程应用中无限供应的细胞来源这一观点。