Clinical Biochemistry and Pharmacology Department, The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
J Cell Mol Med. 2018 Mar;22(3):1992-2000. doi: 10.1111/jcmm.13505. Epub 2018 Feb 7.
The role of extracellular vesicles (EVs) as signal mediators has been described in many biological fields. How many EVs are needed to deliver the desired physiological signal is yet unclear. Using a normal trabecular meshwork (NTM) cell culture exposed to non-pigmented ciliary epithelium (NPCE)-derived EVs, a relevant model for studying the human ocular drainage system, we addressed the EVs dose-response effects on the Wnt signaling. The objective of the study was to investigate the dosing effects of NPCE-derived EVs on TM Wnt signaling. EVs were isolated by PEG 8000 method from NPCE and RPE cells (used as controls) conditioned media. Concentrations were determined by Tunable Resistive Pulse Sensing method. Various exosomes concentration were incubated with TM cells, for the determination of mRNA (β-Catenin, Axin2 and LEF1) and protein (β-Catenin, GSK-3β) expression using real-time quantitative PCR and Western blot, respectively. Exposure of NTM cells for 8 hrs to low EVs concentrations was associated with a significant decreased expression of β-Catenin, GSK-3β, as opposed to exposure to high exosomal concentrations. Pro-MMP9 and MMP9 activities were significantly enhanced in NTM cells treated with high EV concentrations of (X10) as compared to low EV concentrations of either NPCE- or RPE-derived EVs and to untreated control. Our data support the concept that EVs biological effects are concentration-dependent at their target site. Specifically in the present study, we described a general dose-response at the gene and MMPs activity and a different dose-response regarding key canonical Wnt proteins expression.
细胞外囊泡 (EVs) 在许多生物领域作为信号介质的作用已被描述。然而,传递所需生理信号所需的 EV 数量尚不清楚。使用暴露于非色素睫状上皮 (NPCE) 衍生的 EV 的正常小梁网 (NTM) 细胞培养物,这是研究人眼引流系统的相关模型,我们研究了 EV 对 Wnt 信号的剂量反应。本研究的目的是研究 NPCE 衍生的 EV 对 TM Wnt 信号的剂量作用。通过 PEG 8000 方法从 NPCE 和 RPE 细胞(用作对照)的条件培养基中分离 EVs,并通过可调电阻脉冲感应法测定浓度。将各种外泌体浓度与 TM 细胞孵育,分别使用实时定量 PCR 和 Western blot 测定 mRNA(β-连环蛋白、Axin2 和 LEF1)和蛋白质(β-连环蛋白、GSK-3β)的表达。将 NTM 细胞暴露于低 EV 浓度 8 小时与β-连环蛋白、GSK-3β 的表达显著降低有关,而与高外泌体浓度相比则相反。与低 EV 浓度的 NPCE 或 RPE 衍生的 EV 相比,高 EV 浓度(X10)处理的 NTM 细胞中的 Pro-MMP9 和 MMP9 活性显著增强,与未处理的对照相比也是如此。我们的数据支持 EV 生物效应在其靶部位呈浓度依赖性的概念。具体而言,在本研究中,我们描述了基因和 MMPs 活性的一般剂量反应,以及关键经典 Wnt 蛋白表达的不同剂量反应。