Delinassios J G, Kottaridis S D
Biol Cell. 1984;50(1):9-16. doi: 10.1111/j.1768-322x.1984.tb00250.x.
Affinity toward each other was demonstrated in co-cultures between HeLa cells and fibroblasts originating from human tumor stromal or normal tissues. Both cell types in the mixed cultures (ratio 1:1, 1:2, 2:1) proliferated normally as shown by 3H-thymidine labeling index estimation for up to 48 hr of co-culture. At ratios of fibroblasts: HeLa lower than 1:10, fibroblasts were eventually eliminated after serial passaging. It was shown that 3H-nucleotides could be transferred between heterologous cells in either direction. Contact of cells was essential for this phenomenon. Transfer of the label from HeLa to fibroblasts required a longer interaction time and was evidently lower than the transfer from fibroblasts to HeLa. 3H-thymidine incorporated into the DNA of either cell type could not be transferred from one cell to another. The model provides a means for studying neoplastic X normal (or tumour stromal) cell interactions in vitro.
在源自人类肿瘤基质或正常组织的成纤维细胞与HeLa细胞的共培养中,二者表现出相互亲和性。混合培养物中的两种细胞类型(比例为1:1、1:2、2:1)均正常增殖,共培养长达48小时的3H-胸腺嘧啶核苷标记指数估算结果表明了这一点。当成纤维细胞与HeLa细胞的比例低于1:10时,经过连续传代后,成纤维细胞最终会被清除。结果表明,3H-核苷酸可在异源细胞之间双向转移。细胞接触是这一现象的必要条件。标记从HeLa细胞转移至成纤维细胞需要更长的相互作用时间,且明显低于从成纤维细胞转移至HeLa细胞的情况。掺入任何一种细胞类型DNA中的3H-胸腺嘧啶核苷都无法从一个细胞转移至另一个细胞。该模型为体外研究肿瘤细胞与正常(或肿瘤基质)细胞的相互作用提供了一种方法。