Müller-Glauser W, Preisig E
Arch Oral Biol. 1983;28(8):765-71. doi: 10.1016/0003-9969(83)90113-9.
Human epithelial cells isolated from adult gingival and infant palatal biopsies were cultured using 3T3 feeder cells. The colony-forming efficiency was about 0.8 per cent with cholera toxin and epidermal growth factor (EGF). The cell yield of cultures from infant palates depended on the concentration of cholera toxin and the presence of EGF in the culture medium; the culture lifetime and the number of cell generations were higher for oral epithelial cells originating from infants than from adults; the mean thickness of well-developed areas was 15 micron in control cultures and slightly smaller with cholera toxin and EGF. It is concluded that cultivation of epithelial cells from the human oral mucosa is easier with culture media containing cholera toxin and EGF. The same is true for cells originating from infants rather than from adults.
从成人牙龈和婴儿腭部活检组织中分离出的人上皮细胞,使用3T3饲养层细胞进行培养。在霍乱毒素和表皮生长因子(EGF)存在的情况下,集落形成效率约为0.8%。来自婴儿腭部的培养物的细胞产量取决于霍乱毒素的浓度和培养基中EGF的存在;源自婴儿的口腔上皮细胞的培养寿命和细胞代数高于源自成人的细胞;在对照培养物中,发育良好区域的平均厚度为15微米,在添加霍乱毒素和EGF的情况下略小。结论是,使用含有霍乱毒素和EGF的培养基培养人口腔黏膜上皮细胞更容易。对于源自婴儿而非成人的细胞也是如此。