Division of Veterinary Anatomy, Vetsuisse Faculty, University of Bern, 3012 Bern, Switzerland.
Institute of Parasitology, Vetsuisse Faculty, University of Bern, 3012 Bern, Switzerland.
Int J Mol Sci. 2020 May 27;21(11):3799. doi: 10.3390/ijms21113799.
Small extracellular vesicles (EVs) are among the most frequently investigated EVs and play major roles in intercellular communication by delivering various cargo molecules to target cells. They could potentially represent an alternative delivery strategy to treat ocular toxoplasmosis, a parasitosis affecting the retinal pigment epithelium (RPE). To date, the uptake of human small EVs by RPE cells has never been reported. In this study, we report on the intracellular uptake of fluorescently labelled human urine and fibroblast-derived small EVs by human RPE cells. In summary, both dye-labelled urinary small EVs and small EVs obtained from fibroblasts stably expressing membrane-bound green fluorescent protein were successfully internalized by RPE cells as revealed by immunohistochemistry. In recipient ARPE19 cells, BODIPY-labelled small EVs were found in close vicinity to the parasite Additionally, an ultrastructural method was enabled to distinguish between labelled exogenous and endogenous small EVs within target cells.
小细胞外囊泡 (EVs) 是最常被研究的 EVs 之一,通过向靶细胞递各种货物分子在细胞间通讯中发挥主要作用。它们可能代表了一种替代的眼部弓形虫病治疗的递药策略,眼部弓形虫病是一种影响视网膜色素上皮 (RPE) 的寄生虫病。迄今为止,尚未有报道表明 RPE 细胞摄取人小 EVs。在本研究中,我们报告了人 RPE 细胞对内源性和外源性荧光标记的人尿和成纤维细胞来源的小 EVs 的摄取。总之,免疫组织化学显示,染料标记的尿小 EVs 和稳定表达膜结合绿色荧光蛋白的成纤维细胞来源的小 EVs 均被 RPE 细胞成功内化。在接受 ARPE19 细胞中,BODIPY 标记的小 EVs 被发现与寄生虫紧密相邻。此外,一种超微结构方法能够区分靶细胞内标记的外源性和内源性小 EVs。