Department of Biomedical Engineering, The Ohio State University, 270 Bevis Hall, 1080 Carmack Rd., Columbus, OH 43210, USA.
Lab Chip. 2012 Nov 7;12(21):4424-32. doi: 10.1039/c2lc40726d.
Guided cell migration plays a crucial role in tumor metastasis, which is considered to be the major cause of death in cancer patients. Such behavior is regulated in part by micro/nanoscale topographical cues present in the parenchyma or stroma in the form of fiber-like and/or conduit-like structures (e.g., white matter tracts, blood/lymphatic vessels, subpial and subperitoneal spaces). In this paper we used soft lithography micromolding to develop a tissue culture polystyrene platform with a microscale surface pattern that was able to induce guided cell motility along/through fiber-/conduit-like structures. The migratory behaviors of primary (glioma) and metastatic (lung and colon) tumors excised from the brain were monitored via time-lapse microscopy at the single cell level. All the tumor cells exhibited axially persistent cell migration, with percentages of unidirectionally motile cells of 84.0 ± 3.5%, 58.3 ± 6.8% and 69.4 ± 5.4% for the glioma, lung, and colon tumor cells, respectively. Lung tumor cells showed the highest migratory velocities (41.8 ± 4.6 μm h(-1)) compared to glioma (24.0 ± 1.8 μm h(-1)) and colon (26.7 ± 2.8 μm h(-1)) tumor cells. This platform could potentially be used in conjunction with other biological assays to probe the mechanisms underlying the metastatic phenotype under guided cell migration conditions, and possibly by itself as an indicator of the effectiveness of treatments that target specific tumor cell motility behaviors.
导向细胞迁移在肿瘤转移中起着至关重要的作用,而肿瘤转移被认为是癌症患者死亡的主要原因。这种行为部分受到微/纳米级表面形貌的调节,这些形貌以纤维状和/或管状结构的形式存在于实质或基质中(例如,白质束、血管/淋巴管、软脑膜下和腹膜下空间)。在本文中,我们使用软光刻微模塑技术开发了一种具有微尺度表面图案的组织培养聚苯乙烯平台,该平台能够诱导细胞沿着/穿过纤维/管状结构进行导向迁移。通过时差显微镜在单细胞水平监测从大脑中切除的原发性(神经胶质瘤)和转移性(肺和结肠)肿瘤的迁移行为。所有肿瘤细胞均表现出轴向持续的细胞迁移,其中定向迁移的细胞百分比分别为神经胶质瘤、肺和结肠肿瘤细胞的 84.0±3.5%、58.3±6.8%和 69.4±5.4%。与神经胶质瘤(24.0±1.8 μm h(-1))和结肠(26.7±2.8 μm h(-1))肿瘤细胞相比,肺肿瘤细胞表现出最高的迁移速度(41.8±4.6 μm h(-1))。该平台可与其他生物测定法结合使用,以探究在导向细胞迁移条件下转移表型的潜在机制,并且可能本身就是针对特定肿瘤细胞迁移行为的治疗效果的指标。