Sammarco A, Finesso G, Cavicchioli L, Ferro S, Caicci F, Zanetti R, Sacchetto R, Zappulli V
Department of Comparative Biomedicine and Food Science, University of Padua, Padua, Italy.
Department of Biology, University of Padua, Padua, Italy.
Vet Comp Oncol. 2018 Dec;16(4):489-496. doi: 10.1111/vco.12405. Epub 2018 May 30.
Extracellular vesicles (EVs) are membrane-bound vesicles produced by cells, known to play a key role in cell-to-cell communication. They exert pleiotropic biological functions via the horizontal transfer of bioactive molecules (DNA, RNAs, proteins, and lipids) within the tumour microenvironment and throughout the body. In human cancer, EVs are known to interfere with pathways that lead to tumour progression and are used as novel cancer biomarkers. In veterinary medicine, very little is known on cancer-derived EVs. In this study, we preliminarily characterized EVs in mammary gland cancer of dogs and cats. EVs were isolated by ultracentrifugation from canine (CYPp), feline (FMCp) and human (MCF7) mammary tumour cell lines. EVs were visualized by transmission electron microscopy (TEM), counted using nanoparticle tracking analysis (NTA) and characterized by immunogold (CD63 and Alix) and western blot (Alix and TSG101). Additionally, EV production by "donor" cells (palmtdTomato ) and uptake by "recipient" cells (GFP ) were assessed. EVs were successfully isolated from all 3 cell lines by ultracentrifugation. Membrane-bound structures (50-400 nm) were identified by TEM and were positive for both CD63 and Alix at immunogold. Western blot showed positivity of EVs to Alix and TSG101. NTA analysis detected EVs from cell culture media ranging from 1.67 to 2.56 × 10 as number of EVs/cell and from 80 to 600 nm in size. Confocal microscopy identified the presence of palmtdTomato EVs into the cytoplasm of GFP cells. This preliminary study identified and characterized canine and feline mammary tumour cell-derived EVs, opening in veterinary medicine a new interesting unexplored field with several applications and limitless potential.
细胞外囊泡(EVs)是细胞产生的膜结合囊泡,已知在细胞间通讯中起关键作用。它们通过在肿瘤微环境和全身水平转移生物活性分子(DNA、RNA、蛋白质和脂质)发挥多效性生物学功能。在人类癌症中,已知细胞外囊泡会干扰导致肿瘤进展的途径,并被用作新型癌症生物标志物。在兽医学中,关于癌症来源的细胞外囊泡知之甚少。在本研究中,我们初步表征了犬猫乳腺癌中的细胞外囊泡。通过超速离心从犬(CYPp)、猫(FMCp)和人(MCF7)乳腺肿瘤细胞系中分离出细胞外囊泡。通过透射电子显微镜(TEM)观察细胞外囊泡,使用纳米颗粒跟踪分析(NTA)进行计数,并通过免疫金(CD63和Alix)和蛋白质印迹(Alix和TSG101)进行表征。此外,评估了“供体”细胞(palmtdTomato)产生细胞外囊泡以及“受体”细胞(GFP)摄取细胞外囊泡的情况。通过超速离心成功从所有3种细胞系中分离出细胞外囊泡。通过TEM鉴定出膜结合结构(50 - 400nm),免疫金检测显示其CD63和Alix均呈阳性。蛋白质印迹显示细胞外囊泡对Alix和TSG101呈阳性。NTA分析检测到细胞培养基中的细胞外囊泡数量为1.67至2.56×10个/细胞,大小在80至600nm之间。共聚焦显微镜鉴定出palmtdTomato细胞外囊泡存在于GFP细胞的细胞质中。这项初步研究鉴定并表征了犬猫乳腺肿瘤细胞来源的细胞外囊泡,在兽医学领域开启了一个新的有趣的未探索领域,具有多种应用和无限潜力。