Sipos Bence, Möser Simone, Kalthoff Holger, Török Virag, Löhr Matthias, Klöppel Günter
Department of Pathology, University of Kiel, Germany.
Virchows Arch. 2003 May;442(5):444-52. doi: 10.1007/s00428-003-0784-4. Epub 2003 Apr 12.
There are a large number of stable pancreatic ductal carcinoma cell lines that are used by researchers worldwide. Detailed data about their differentiation status and growth features are, however, often lacking. We therefore attempted to classify commonly used pancreatic carcinoma cell lines according to defined cell biological criteria. Twelve pancreatic ductal adenocarcinoma cell lines were cultured as monolayers and spheroids and graded according to their ultrastructural features. The grading system was based on the integrity of membrane structures and on the presence of mucin granules, cell organelles, nuclear and cellular polymorphism, cell polarity, and lumen formation. On the basis of the resulting scores the cell lines were classified as well, moderately, or poorly differentiated. In addition, immunocytochemistry was performed for the markers cytokeratin 7, 8, 18, 19, carcinoembryonic antigen, MUC1 MUC2, MUC5, and MUC6. The population doubling time of monolayer cultures, determined by a tetrazolium salt based proliferation assay was correlated with the ultrastructural grade. The grading of the ultrastructural features of the monolayers, and particularly of the spheroids, revealed that Capan-1 and Capan-2 cells were well differentiated; Colo357, HPAF-2, Aspc-1, A818-4, BxPc3, and Panc89 cells were moderately differentiated and PancTu-I, Panc1, Pt45P1, and MiaPaCa-2 cells poorly differentiated. Membrane-bound MUC1 staining was a characteristic of well differentiated cell lines. The population doubling time of the monolayer cultures was related to the differentiation grade. No relationship was found between the p53, K-ras, DPC4/Smad4, or p16(INK4a) mutation status and the grade of differentiation. We conclude that the proposed ultrastructural grading system combined with the proliferative activity provides a basis for further comparative studies of pancreatic ductal adenocarcinoma cell lines.
全球研究人员使用着大量稳定的胰腺导管癌细胞系。然而,关于它们分化状态和生长特征的详细数据常常缺失。因此,我们尝试根据既定的细胞生物学标准对常用的胰腺癌细胞系进行分类。将12种胰腺导管腺癌细胞系培养成单层细胞和球体,并根据其超微结构特征进行分级。该分级系统基于膜结构的完整性以及黏蛋白颗粒、细胞器、核及细胞多态性、细胞极性和管腔形成的情况。根据所得分数,将细胞系分为高分化、中分化或低分化。此外,还对细胞角蛋白7、8、18、19、癌胚抗原、MUC1、MUC2、MUC5和MUC6等标志物进行了免疫细胞化学检测。通过基于四氮唑盐的增殖试验测定的单层培养物的群体倍增时间与超微结构分级相关。单层细胞尤其是球体的超微结构特征分级显示,Capan-1和Capan-2细胞为高分化;Colo357、HPAF-2、Aspc-1、A818-4、BxPc3和Panc89细胞为中分化,而PancTu-I、Panc1、Pt45P1和MiaPaCa-2细胞为低分化。膜结合MUC1染色是高分化细胞系的特征。单层培养物的群体倍增时间与分化程度有关。未发现p53、K-ras、DPC4/Smad4或p16(INK4a)突变状态与分化程度之间存在关联。我们得出结论,所提出的超微结构分级系统结合增殖活性为进一步比较研究胰腺导管腺癌细胞系提供了基础。