INSERM UMR_S1109, Strasbourg 67200, France; Université de Strasbourg, Strasbourg 67200, France; Fédération de Médecine Translationnelle de Strasbourg, Strasbourg 67200, France; CNRS SNC5055, Strasbourg 67200, France.
INSERM UMR_S1109, Strasbourg 67200, France; Université de Strasbourg, Strasbourg 67200, France; Fédération de Médecine Translationnelle de Strasbourg, Strasbourg 67200, France.
Dev Cell. 2019 Feb 25;48(4):554-572.e7. doi: 10.1016/j.devcel.2019.01.014. Epub 2019 Feb 7.
Tumor extracellular vesicles (EVs) mediate the communication between tumor and stromal cells mostly to the benefit of tumor progression. Notably, tumor EVs travel in the bloodstream, reach distant organs, and locally modify the microenvironment. However, visualizing these events in vivo still faces major hurdles. Here, we describe an approach for tracking circulating tumor EVs in a living organism: we combine chemical and genetically encoded probes with the zebrafish embryo as an animal model. We provide a first description of tumor EVs' hemodynamic behavior and document their intravascular arrest. We show that circulating tumor EVs are rapidly taken up by endothelial cells and blood patrolling macrophages and subsequently stored in degradative compartments. Finally, we demonstrate that tumor EVs activate macrophages and promote metastatic outgrowth. Overall, our study proves the usefulness and prospects of zebrafish embryo to track tumor EVs and dissect their role in metastatic niches formation in vivo.
肿瘤细胞外囊泡(EVs)主要通过促进肿瘤进展在肿瘤细胞和基质细胞之间进行通讯。值得注意的是,肿瘤 EVs 会在血液中循环,到达远处的器官,并在局部改变微环境。然而,在活体中观察这些事件仍然面临重大障碍。在这里,我们描述了一种在活体中追踪循环肿瘤 EVs 的方法:我们将化学和基因编码探针与斑马鱼胚胎结合作为动物模型。我们提供了肿瘤 EVs 血流动力学行为的初步描述,并记录了它们的血管内停滞。我们表明,循环肿瘤 EVs 被内皮细胞和血液巡逻巨噬细胞迅速摄取,并随后储存在降解性隔室中。最后,我们证明肿瘤 EVs 激活巨噬细胞并促进转移生长。总的来说,我们的研究证明了斑马鱼胚胎在追踪肿瘤 EVs 并在体内解析其在转移龛形成中的作用方面的有用性和前景。