Fridman R, Scott A F, Muller D, Reich R, Penno M B
Laboratory of Developmental Biology and Anomalies, National Institute of Dental Research, NIH, Bethesda, Md.
Invasion Metastasis. 1990;10(4):208-24.
Using the Matrigel invasion assay, we have examined the role of cell adhesion and migration in the invasiveness of two cell lines, DM and HSR, derived from the Y1 mouse adrenocortical tumor. The DM cells were metastatic and more invasive (10-fold) than the nonmetastatic HSR cells. The difference in invasiveness could not be ascribed to different levels of secreted type IV collagenolytic activity since HSR cells secreted higher levels of activity. Cells from the metastatic DM line showed greater motility to both laminin and fibronectin when compared to the HSR line. Furthermore, both Matrigel and laminin promoted the attachment and spreading of DM cells but they had little effect on the adhesion of the HSR cells. Electron microscopic examination revealed an increased ruffling of the cell membrane in the metastatic DM line. These studies suggest a role for cell adhesion and migration on the invasion of Matrigel by malignant tumor cells.
利用基质胶侵袭试验,我们研究了细胞黏附和迁移在源自Y1小鼠肾上腺皮质肿瘤的两种细胞系DM和HSR侵袭性中的作用。DM细胞具有转移性,其侵袭性比非转移性HSR细胞高(10倍)。侵袭性的差异不能归因于分泌型IV型胶原酶活性水平的不同,因为HSR细胞分泌的活性水平更高。与HSR细胞系相比,转移性DM细胞系的细胞对层粘连蛋白和纤连蛋白均表现出更大的运动性。此外,基质胶和层粘连蛋白均促进了DM细胞的附着和铺展,但对HSR细胞的黏附作用很小。电子显微镜检查显示,转移性DM细胞系中细胞膜的皱褶增加。这些研究表明细胞黏附和迁移在恶性肿瘤细胞侵袭基质胶过程中发挥作用。