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Role of Autophagy in Hypoxia-Induced Angiogenesis of RF/6A Cells in vitro

机译:自噬在缺氧诱导的RF / 6A细胞血管生成中的作用

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Purpose: Autophagy plays a role in the pathogenesis of tumor angiogenesis and cardiovascular diseases. The autophagy level in mammalian cells was found to increase in the state of hypoxia or ischemia reperfusion. However, the role of autophagy in ocular angiogenesis has not yet been elucidated. The aim of this study was to investigate the effects of autophagy on hypoxia-induced choroidal and retinal angiogenesis in vitro using a rhesus macaque choroid-retinal endothelial (RF/6A) cell line.Materials and Methods: RF/6A cells were cultured and randomly divided into three groups according to the different culture media: control, hypoxia model[adding 125Mcobalt chloride (CoCl2) to the culture medium], and hypoxia with an autophagy inhibition group [pretreatment with 5 mmol/L 3-methyladenine (3-MA) for 1.5 h and then adding125mol/LCoCl2 to the culture medium]. The impact of 3-MA's effect on the level of autophagy proteins (Beclin-1 and LC3) was tested by Western blot analysis. The cell proliferation was assessed using the chromogenicmethylthiazol tetrazolium bromide (MTT) dye after 24 and 48 hours. Cell migration was investigated by wound assay. The tube formation was measured on Matrigel.Results: Under chemical hypoxia conditions, Beclin-1 and LC3 levels increased and this change can be inhibited by 3-MA. Cell viability was decreased in cells treated with CoCl2 for 24 and 48 h compared with the control, and pretreatment with 3-MA slightly promoted CoCl2-inhibited cell proliferation. Cell migration and tube formation were increased in cells treated with CoCl2 for 24 and 48 h compared with the control. Pretreatment with 3-MA significantly inhibited CoCl2-induced cell migration and tube formation.Conclusions: Hypoxia-induced autophagy decreased the cell viability and increased the cell migration and tube formation of RF/6A cells. 3-MA can inhibit hypoxia-induced angiogenesis of RF/6A cells in vitro. The present study suggests that autophagy plays a role in retinal and choroidal angiogenesis and the autophagy inhibitor can be a potential candidate for the treatment of choroidal or retinal neovascularization.
机译:目的:自噬在肿瘤血管生成和心血管疾病的发病机制中起作用。发现哺乳动物细胞中的自噬水平增加缺氧或缺血再灌注状态。然而,自噬在眼血管生成中的作用尚未阐明。本研究的目的是使用恒河猴脉络膜视网膜内皮(RF / 6A)细胞系来研究自噬对缺氧诱导的脉络膜和视网膜血管生成的影响。方法和方法:培养和随机培养RF / 6A细胞根据不同的培养基分为三组:对照,缺氧模型[将125mcogogalt氯化物(COCl2)加入培养基],缺氧具有自噬抑制基团[预处理5mmol / L 3-甲基腺嘌呤(3-MA)对于1.5小时,然后加入125mol / LcoCl2至培养基]。通过蛋白质印迹分析测试3-MA对自噬蛋白水平(BECLIN-1和LC3)的影响。在24至48小时后使用色原甲基噻唑四唑溴铵(MTT)染料评估细胞增殖。通过伤口测定研究细胞迁移。在Matrigel上测量管形成。结果:在化学缺氧条件下,BECLIN-1和LC3水平增加,并且通过3-mA可以抑制这种变化。用COCl2处理24和48小时的细胞中细胞活力降低,与对照相比,并用3-mA略有促进的COCl2抑制细胞增殖预处理。与对照相比,用COCl2处理24和48小时处理的细胞中细胞迁移和管形成。 3-mA的预处理显着抑制了COCl2诱导的细胞迁移和管形成。结论:缺氧诱导的自噬降低降低细胞活力并增加了RF / 6A细胞的细胞迁移和管形成。 3- mA可以在体外抑制缺氧诱导的RF / 6A细胞血管生成。本研究表明,自噬在视网膜和脉络膜血管生成中发挥作用,并且自噬抑制剂可以是治疗脉络膜或视网膜新生血管的潜在候选者。

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