Vasil'ev A V, Voroteliak E A, Terskikh V V
Ontogenez. 1994 May-Jun;25(3):74-9.
A population of basal keratinocytes was obtained by removing suprabasal cells from multilayered cultures of human epidermal keratinocytes after their incubation in medium 199 without Ca2+, serum, and mitogens (insulin, EGF, and isoproterenol). The addition of EGF (10 ng/ml) to fresh DMEM: F12 medium with cultured basal keratinocytes stimulated [3H]thymidine incorporation into cells. Serum added to the medium also stimulated this process. However, the addition of both serum and EGF did not result in any further increase in label incorporation. It was also shown that serum promotes stratification of cultures and differentiation of basal keratinocytes, whereas EGF counteracts this effect.
通过在不含Ca2+、血清和促有丝分裂原(胰岛素、表皮生长因子和异丙肾上腺素)的199培养基中孵育人表皮角质形成细胞多层培养物,去除基底上层细胞,获得了一群基底角质形成细胞。向含有培养的基底角质形成细胞的新鲜DMEM:F12培养基中添加表皮生长因子(10 ng/ml)可刺激[3H]胸苷掺入细胞。向培养基中添加血清也可刺激这一过程。然而,同时添加血清和表皮生长因子并不会导致标记掺入的进一步增加。还表明,血清促进培养物分层和基底角质形成细胞分化,而表皮生长因子则抵消这种作用。