Lu Jinjin, Zheng Xiufen, Li Fan, Yu Yang, Chen Zhong, Liu Zheng, Wang Zhihua, Xu Hua, Yang Weimin
Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, P. R. China.
Department of Pathology, Department of Oncology, Department of Surgery, Western University, Lawson Health Research Institute, London, Ontario, N6A 5A5, Canada.
Oncotarget. 2017 Feb 28;8(9):15539-15552. doi: 10.18632/oncotarget.14695.
Intercellular transfer of organelles via tunneling nanotubes (TNTs) is a novel means of cell-to-cell communication. Here we demonstrate the existence of TNTs between co-cultured RT4 and T24 bladder cancer cells using light microscopy, fluorescence imaging, and scanning electron microscopy (SEM). Spontaneous unidirectional transfer of mitochondria from T24 to RT4 cells was detected using fluorescence imaging and flow cytometry. The distribution of mitochondria migrated from T24 cells was in good agreement with the original mitochondria in RT4 cells, which may imply mitochondrial fusion. We detected cytoskeleton reconstruction in RT4-Mito-T24 cells by observing F-actin redistribution. Akt, mTOR, and their downstream mediators were activated and increased. The resultant increase in the invasiveness of bladder cancer cells was detected in vitro and in vivo. These data indicate that TNTs promote intercellular mitochondrial transfer between heterogeneous cells, followed by an increase in the invasiveness of bladder cancer cells.
通过隧道纳米管(TNTs)进行细胞器的细胞间转移是一种新型的细胞间通讯方式。在此,我们利用光学显微镜、荧光成像和扫描电子显微镜(SEM)证明了共培养的RT4和T24膀胱癌细胞之间存在TNTs。使用荧光成像和流式细胞术检测到线粒体从T24细胞自发单向转移至RT4细胞。从T24细胞迁移来的线粒体分布与RT4细胞中原有的线粒体高度一致,这可能意味着线粒体融合。通过观察F-肌动蛋白重新分布,我们检测到RT4-Mito-T24细胞中的细胞骨架重建。Akt、mTOR及其下游介质被激活并增加。在体外和体内均检测到膀胱癌细胞侵袭性的相应增加。这些数据表明,TNTs促进异质性细胞间的线粒体转移,随后膀胱癌细胞的侵袭性增加。