12,13-二癸酸佛球诱导正常人细胞生长特性的改变。

In Vitro Pub Date : 1984-05-01 DOI:10.1007/BF02619587
R W Trewyn, H B Gatz
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引用次数: 3

摘要

肿瘤启动子phorbol 12,13-didecanoate (PDD)在体外培养培养基中显著改变了早期正常人皮肤细胞的生长特性,培养基中添加了高浓度的选定氨基酸。用10(-7)或10(-8)M PDD连续处理细胞,导致饱和密度在传代早期增加5至10倍,长期增加2至4倍。pdd处理的培养物在细胞密度比对照培养物高10倍以上时保持指数增长。当细胞处于高细胞密度时,从培养基中去除PDD,在随后的传代中使细胞恢复到接近正常的饱和密度。PDD也以剂量依赖的方式促进正常人细胞在甲基纤维素中的锚定独立生长,在PDD存在的情况下进行传代培养需要最大的集落形成。结构类似物4 α -phorbol 12,13-didecanoate未能引起类似的细胞反应。
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Altered growth properties of normal human cells induced by phorbol 12,13-didecanoate.

The tumor promoter phorbol 12,13-didecanoate (PDD) significantly altered the growth properties of early passage normal human skin cells in vitro in culture medium supplemented with elevated concentrations of selected amino acids. Continuous treatment of cells with 10(-7) or 10(-8) M PDD resulted in a 5 to 10-fold increase in saturation density at early passages followed by a long-term two- to fourfold increase. The PDD-treated cultures remained in exponential growth at cell densities greater than 10-fold higher than the control cultures. Removal of PDD from the culture medium while the cells were at a high cell density resulted in a return to near-normal saturation density by the subsequent passage. Anchorage independent growth of normal human cells in methylcellulose was also promoted by PDD in a dose dependent manner, with prior subculturing in the presence of PDD being required for maximal colony formation. The structural analog 4 alpha-phorbol 12,13-didecanoate failed to elicit similar cellular responses.

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