Nannmark U, Blomqvist G, Braide M, Johansson B R, Bagge U
Department of Anatomy, University of Göteborg, Sweden.
Cell Biophys. 1990 Oct;17(2):153-61. doi: 10.1007/BF02990494.
Earlier studies have shown a lower degree of lodgement and early survival of tumor cells in muscle than in liver after infusion via the femoral artery and portal vein, respectively. A possible explanation to this difference might be that the tumor cells are mechanically destroyed, and thus die more rapidly in muscle because they enter this capillary network at a much higher flow velocity. In the present study, the effect on early tumor cell (rat fibrosarcoma) survival of a high and a low flow velocity/deformation rate was evaluated in micropore (5 microns) filters, using isotope (Cr51) technique. These experiments were combined with scanning electron microscopic (SEM) analyses. The filter experiments showed no significant differences in the rate of cell death in the filters between tumor cells subjected to high or low deformation rates, and there were no qualitative differences in tumor cell appearance in the SEM study. It is, therefore, concluded that the difference in tumor cell lodgement and survival between muscle and liver is not primarily caused by differences in the rate of cell deformation upon entry of the organ capillary network.
早期研究表明,分别经股动脉和门静脉注入后,肿瘤细胞在肌肉中的着床程度和早期存活率低于在肝脏中的。对此差异的一种可能解释可能是肿瘤细胞被机械破坏,因此在肌肉中死亡更快,因为它们以更高的流速进入这个毛细血管网络。在本研究中,使用同位素(铬51)技术,在微孔(5微米)滤器中评估了高流速/变形率和低流速/变形率对早期肿瘤细胞(大鼠纤维肉瘤)存活率的影响。这些实验与扫描电子显微镜(SEM)分析相结合。滤器实验表明,经受高变形率或低变形率的肿瘤细胞在滤器中的细胞死亡率没有显著差异,并且在SEM研究中肿瘤细胞外观没有定性差异。因此,得出结论,肌肉和肝脏之间肿瘤细胞着床和存活的差异并非主要由器官毛细血管网络入口处细胞变形率的差异所致。