Clinical Department of Pathology, Medical University of Vienna, Vienna, Austria.
Institute of Science and Technology, Klosterneuburg, Austria.
J Cell Biol. 2018 Jun 4;217(6):2205-2221. doi: 10.1083/jcb.201612051. Epub 2018 Apr 12.
Lymphatic endothelial cells (LECs) release extracellular chemokines to guide the migration of dendritic cells. In this study, we report that LECs also release basolateral exosome-rich endothelial vesicles (EEVs) that are secreted in greater numbers in the presence of inflammatory cytokines and accumulate in the perivascular stroma of small lymphatic vessels in human chronic inflammatory diseases. Proteomic analyses of EEV fractions identified >1,700 cargo proteins and revealed a dominant motility-promoting protein signature. In vitro and ex vivo EEV fractions augmented cellular protrusion formation in a CX3CL1/fractalkine-dependent fashion and enhanced the directional migratory response of human dendritic cells along guidance cues. We conclude that perilymphatic LEC exosomes enhance exploratory behavior and thus promote directional migration of CX3CR1-expressing cells in complex tissue environments.
淋巴管内皮细胞 (LEC) 会释放细胞外趋化因子来引导树突状细胞迁移。在这项研究中,我们报告称,LEC 还会释放富含基底外侧外泌体的内皮小泡 (EEV),在炎症细胞因子存在的情况下,这些小泡会被更多地分泌,并在人类慢性炎症性疾病中小淋巴管的血管周围基质中积累。对 EEV 部分的蛋白质组学分析鉴定出超过 1700 种货物蛋白,并揭示了一个主要的促运动蛋白特征。体外和离体 EEV 部分以依赖 CX3CL1/ fractalkine 的方式增强细胞突起的形成,并增强人树突状细胞沿导向线索的定向迁移反应。我们的结论是,淋巴管周围 LEC 外泌体增强了探索行为,从而促进了表达 CX3CR1 的细胞在复杂组织环境中的定向迁移。