Schuster U, Büttner R, Hofstädter F, Knüchel R
Institute of Pathology, University of Regensburg, Germany.
J Urol. 1994 Jun;151(6):1707-11. doi: 10.1016/s0022-5347(17)35349-1.
Three-dimensional multicellular spheroids of two fibroblast cell lines (WI-38 and N1) and two differently differentiated bladder carcinoma cell lines (RT4 and J82) were used for cocultures of multicellular tumor spheroids with multicellular spheroids of fibroblasts. The aim of the study was the establishment and characterization of a standardized three-dimensional model for studies of tumor cell-fibroblast interaction as one aspect of tumor-stromal cell interactions of in vivo tumor tissue. Interaction of multicellular spheroids of both fibroblast cell types was analyzed by staining with antibodies against cytokeratin, vimentin and different extracellular matrix molecules. Further, proliferation assessment and phenotypic characterization of the cocultures are presented. Interactions varied with tumor cell type and fibroblast cell type, reflecting intrinsic properties of tumor cells and fibroblasts. The coculture of tumor cells with N1 reflected the in vivo situation the closest, since invasive properties of J82 as well as noninvasive properties of RT4 were characteristics seen in coculture.
使用两种成纤维细胞系(WI - 38和N1)以及两种不同分化程度的膀胱癌细胞系(RT4和J82)的三维多细胞球体进行多细胞肿瘤球体与成纤维细胞多细胞球体的共培养。本研究的目的是建立并表征一个标准化的三维模型,用于研究肿瘤细胞 - 成纤维细胞相互作用,这是体内肿瘤组织肿瘤 - 基质细胞相互作用的一个方面。通过用抗细胞角蛋白、波形蛋白和不同细胞外基质分子的抗体染色来分析两种成纤维细胞类型的多细胞球体之间的相互作用。此外,还展示了共培养物的增殖评估和表型特征。相互作用因肿瘤细胞类型和成纤维细胞类型而异,反映了肿瘤细胞和成纤维细胞的内在特性。肿瘤细胞与N1的共培养最接近体内情况,因为在共培养中观察到J82的侵袭特性以及RT4的非侵袭特性。