Zellmer S, Gaunitz F, Salvetter J, Surovoy A, Reissig D, Gebhardt R
Institute of Biochemistry, Medical Faculty, University Leipzig, Germany.
Histochem Cell Biol. 2001 Jan;115(1):41-7. doi: 10.1007/s004180000225.
Normal human epidermal keratinocytes were isolated and cultivated in serum-free medium. The expression of the integrin subunits alpha6 and beta1 indicated that a high number of keratinocytes from the stem cell system was present. These cells were transfected with complexes made of different cationic lipids and marker genes. Effectene showed a 20-fold higher transfection efficiency, compared to Lipofectin and Lipofectamine, and a similar low toxicity. The transfection protocol was optimised. A DNA/lipid ratio of 0.133 showed the highest transfection efficiency. Keratinocytes expressed the marker gene luciferase for 20 days. The maximum expression occurred after 3-4 days, where individual patches of fluorescent keratinocytes were detected. Transfected keratinocytes, cultivated at the air-liquid interface, expressed the marker gene beta-galactosidase for at least 7 weeks.
分离正常人表皮角质形成细胞并在无血清培养基中培养。整合素亚基α6和β1的表达表明存在大量来自干细胞系统的角质形成细胞。用不同阳离子脂质和标记基因制成的复合物转染这些细胞。与Lipofectin和Lipofectamine相比,Effectene的转染效率高20倍,且毒性相似。优化了转染方案。DNA/脂质比为0.133时转染效率最高。角质形成细胞表达标记基因荧光素酶达20天。最大表达在3-4天后出现,此时检测到单个荧光角质形成细胞斑块。在气液界面培养的转染角质形成细胞表达标记基因β-半乳糖苷酶至少7周。