Balcioglu Hayri E, van de Water Bob, Danen Erik H J
Division of Toxicology, Leiden Academic Center for Drug Research, Leiden University, Leiden, the Netherlands.
Sci Rep. 2016 Mar 2;6:22580. doi: 10.1038/srep22580.
Tumor angiogenesis promotes tumor growth and metastasis. Here, we use automated sequential microprinting of tumor and endothelial cells in extracellular matrix (ECM) scaffolds to study its mechanical aspects. Quantitative reflection microscopy shows that tumor spheroids induce radial orientation of the surrounding collagen fiber network up to a distance of five times their radius. Across a panel of ~20 different human tumor cell lines, remote collagen orientation is correlated with local tumor cell migration behavior. Tumor induced collagen orientation requires contractility but is remarkably resistant to depletion of collagen-binding integrins. Microvascular endothelial cells undergo directional migration towards tumor spheroids once they are within the tumor-oriented collagen fiber network. Laser ablation experiments indicate that an intact physical connection of the oriented network with the tumor spheroid is required for mechanical sensing by the endothelial cells. Together our findings indicate that, in conjunction with described activities of soluble angiogenic factors, remote physical manipulation of the ECM network by the tumor can help to steer angiogenesis.
肿瘤血管生成促进肿瘤生长和转移。在此,我们利用在细胞外基质(ECM)支架中对肿瘤细胞和内皮细胞进行自动连续微打印的方法来研究其力学方面。定量反射显微镜显示,肿瘤球体可诱导周围胶原纤维网络呈径向排列,其距离可达球体半径的五倍。在约20种不同的人类肿瘤细胞系中,远处的胶原纤维排列与局部肿瘤细胞迁移行为相关。肿瘤诱导的胶原纤维排列需要收缩性,但对胶原结合整合素的耗竭具有显著抗性。一旦微血管内皮细胞位于肿瘤定向的胶原纤维网络内,它们就会向肿瘤球体进行定向迁移。激光消融实验表明,内皮细胞进行力学感知需要定向网络与肿瘤球体之间保持完整的物理连接。我们的研究结果共同表明,与可溶性血管生成因子的已知活性相结合,肿瘤对ECM网络的远程物理操纵有助于引导血管生成。