Friedman E, Verderame M, Lipkin M, Pollack R
Cancer Res. 1985 Jul;45(7):3236-42.
Primary culture of human colonic biopsies converts the single cell thick epithelial layer from a highly indented sheet in vivo into a flat patch on the surface of a Petri dish. Migration of cells from biopsies in a continuous sheet to form the patch cultures allows the cultured cells in large part to retain the junctional complexes and membrane interdigitations which connect adjacent cells in vivo and therefore to maintain their spatial relationships to neighboring cells. Migration of the cells onto a flat surface also allows visualization of their actin cables (E. Friedman, M. Verderame, S. Winawer, and R. Pollack, Cancer Res., 44: 3040-3050, 1984). Actin organization patterns have been studied in primary patch cultures of colonic epithelial cells from four stages in the development of colon cancer: normal tissue, normal-appearing but preneoplastic cells characteristic of familial polyposis patients, benign tumors or adenomas from familial polyposis patients, and benign and malignant tumors from patients in the general population. Carcinomas exhibited the least number of actin cables, while adenomas contained the greatest concentration. Similar actin patterns were seen in both familial polyposis and nonpolyposis adenomas. The preneoplastic prebenign tumor stage characteristic of familial polyposis patients had less actin cables than either normal cells or benign tumor cells. Thus actin organization loss characterized the transition from the normal colonic epithelial cell to the preneoplastic nontumor cell. The ability to form actin cables was then regained with the transition from the preneoplastic pretumor cell to the benign tumor cell and lost again with the benign tumor to malignant tumor transition. The complexity of these changes in actin organization during the step-wise transformation of colonic epithelial cells was not predicted from the simple model of actin cable loss accompanying fibroblast transformation.
人结肠活检组织的原代培养可将体内单层细胞厚的高度凹陷上皮层转变为培养皿表面的扁平斑块。活检组织中的细胞以连续片状迁移形成斑块培养物,这使得培养的细胞在很大程度上保留了体内连接相邻细胞的连接复合体和膜交错,从而维持它们与相邻细胞的空间关系。细胞迁移到平坦表面上也便于观察其肌动蛋白束(E. 弗里德曼、M. 韦德拉梅、S. 维纳韦尔和R. 波拉克,《癌症研究》,44: 3040 - 3050,1984)。已对结肠癌发展四个阶段的结肠上皮细胞原代斑块培养物中的肌动蛋白组织模式进行了研究:正常组织、家族性息肉病患者特征性的看似正常但癌前的细胞、家族性息肉病患者的良性肿瘤或腺瘤,以及普通人群患者的良性和恶性肿瘤。癌组织中肌动蛋白束数量最少,而腺瘤中浓度最高。在家族性息肉病和非息肉病腺瘤中都观察到了相似的肌动蛋白模式。家族性息肉病患者特征性的癌前良性肿瘤阶段的肌动蛋白束比正常细胞或良性肿瘤细胞都少。因此,肌动蛋白组织的丧失是正常结肠上皮细胞向癌前非肿瘤细胞转变的特征。然后,随着从癌前肿瘤前细胞向良性肿瘤细胞的转变,形成肌动蛋白束的能力得以恢复,而随着从良性肿瘤向恶性肿瘤的转变又再次丧失。在结肠上皮细胞逐步转变过程中这些肌动蛋白组织变化的复杂性并非由成纤维细胞转变时伴随的肌动蛋白束丧失这一简单模型所预测。