Furukawa M, Kono T, Tanii T, Ishii M, Hamada T, Shibata T
Department of Dermatology, Osaka City University Medical School, Japan.
J Dermatol. 1990 May;17(5):297-302. doi: 10.1111/j.1346-8138.1990.tb01644.x.
As the first step in developing an in vitro model of melanoma cells infiltrating the dermis, B16 murine melanoma cells were cultured on and in type I collagen gels. Under these conditions, the melanoma cell adopted an elongated or dendritic form. Cell proliferation was suppressed in the culture system using the collagen gel as compared with the conventional monolayer culture on plastic. Microcinematographically, this suppression was found to be due to an extension of the cell cycle time of each individual cell. On the other hand, there were no appreciable differences in proliferation pattern between the cells cultured on type I and IV collagen film and those cultured on plastic. These results suggest that there are interactions between type I collagen in the gel form and melanoma cells, especially with respect to cell growth.
作为建立黑色素瘤细胞浸润真皮体外模型的第一步,将B16小鼠黑色素瘤细胞培养在I型胶原凝胶上及其中。在这些条件下,黑色素瘤细胞呈现出细长或树突状形态。与在塑料上的传统单层培养相比,使用胶原凝胶的培养系统中细胞增殖受到抑制。通过显微电影摄影术发现,这种抑制是由于每个细胞的细胞周期时间延长所致。另一方面,在I型和IV型胶原膜上培养的细胞与在塑料上培养的细胞之间在增殖模式上没有明显差异。这些结果表明,凝胶形式的I型胶原与黑色素瘤细胞之间存在相互作用,尤其是在细胞生长方面。