Morsczeck Christian, Ernst Wolfgang, Florian Christian, Reichert Torsten Eugen, Proff Peter, Bauer Richard, Müller-Richter Urs, Driemel Oliver
Institut für Humangenetik, Universität Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg, Germany.
Oral Maxillofac Surg. 2008 Jul;12(2):89-92. doi: 10.1007/s10006-008-0111-y. Epub 2008 Jun 3.
Undifferentiated human dental cells and especially human dental follicle cells are interesting for potential dental treatments. These somatic stem cells are cultured usually in cell culture medium containing bovine serum. In the age of bovine spongiform encephalopathy (BSE), a serum-free cell culture system for dental follicle cells are recommended, if these cells will be applied in dentistry.
However, less is known about the cultivation of dental follicle cells in serum-replacement medium. In this study, we cultivated dental follicle cells in serum-free cell culture medium, which is normally applied for neuronal stem/progenitor cells.
Dental follicle cells were cultivated in both serum-free and serum-containing cell culture media, and gene expression profiles were recorded for connective tissue markers collagen type I and type III and for the human dental follicle cell marker nestin.
It is interesting to note that the gene expressions of collagens and nestin were similar after applying both cell culture conditions.
Although the gene expression of dental follicle cell markers was unchanged, a more appropriate serum-free cell culture medium is recommended for cell proliferation of dental follicle cells.
未分化的人牙细胞,尤其是人牙囊细胞,对于潜在的牙科治疗具有重要意义。这些体细胞干细胞通常在含有牛血清的细胞培养基中培养。在牛海绵状脑病(BSE)时代,如果这些细胞将应用于牙科领域,推荐使用无血清细胞培养系统来培养牙囊细胞。
然而,关于在血清替代培养基中培养牙囊细胞的研究较少。在本研究中(此处“in this study”原译文位置有误,应提前),我们使用通常用于神经干细胞/祖细胞的无血清细胞培养基培养牙囊细胞。
在无血清和含血清的细胞培养基中培养牙囊细胞,并记录结缔组织标志物I型和III型胶原蛋白以及人牙囊细胞标志物巢蛋白的基因表达谱。
值得注意的是,在两种细胞培养条件下,胶原蛋白和巢蛋白的基因表达相似。
虽然牙囊细胞标志物的基因表达没有变化,但推荐使用更合适的无血清细胞培养基来促进牙囊细胞的增殖。