Children's Research Institute and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Children's Research Institute and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Neurology, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China.
Cell Rep. 2020 Feb 25;30(8):2489-2500.e5. doi: 10.1016/j.celrep.2020.01.089.
Emerging evidence suggests that crosstalk between glioma cells and the brain microenvironment may influence brain tumor growth. To date, known reciprocal interactions among these cells have been limited to the release of paracrine factors. Combining a genetic strategy with longitudinal live imaging, we find that individual gliomas communicate with distinct sets of non-glioma cells, including glial cells, neurons, and vascular cells. Transfer of genetic material is achieved mainly through extracellular vesicles (EVs), although cell fusion also plays a minor role. We further demonstrate that EV-mediated communication leads to the increase of synaptic activity in neurons. Blocking EV release causes a reduction of glioma growth in vivo. Our findings indicate that EV-mediated interaction between glioma cells and non-glioma brain cells alters the tumor microenvironment and contributes to glioma development.
新出现的证据表明,胶质瘤细胞与脑微环境之间的串扰可能会影响脑肿瘤的生长。迄今为止,这些细胞之间已知的相互作用仅限于旁分泌因子的释放。通过将遗传策略与纵向活体成像相结合,我们发现单个胶质瘤与不同的非胶质瘤细胞(包括神经胶质细胞、神经元和血管细胞)相互交流。遗传物质的转移主要通过细胞外囊泡(EVs)实现,尽管细胞融合也起次要作用。我们进一步证明,EV 介导的通讯导致神经元中突触活性的增加。阻断 EV 的释放会导致体内胶质瘤生长减少。我们的研究结果表明,胶质瘤细胞与非神经胶质脑细胞之间的 EV 介导的相互作用改变了肿瘤微环境并促进了胶质瘤的发展。