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

机译:自噬在体外低氧诱导的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理中起作用。发现哺乳动物细胞中的自噬水平在缺氧或局部缺血再灌注状态下增加。然而,自噬在眼血管生成中的作用尚未阐明。本研究的目的是通过恒河猴猕猴脉络膜视网膜血管内皮细胞(RF / 6A)研究自噬在体外低氧诱导的脉络膜和视网膜血管生成中的作用。材料与方法: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[向培养基中添加125M氯化钴(CoCl2)]和带有自噬抑制基团的缺氧[5 mmol / L 3-甲基腺嘌呤(3-MA)预处理保持1.5小时,然后向培养基中加入125mol / LCoCl 2。通过蛋白质印迹分析测试了3-MA对自噬蛋白(Beclin-1和LC3)水平的影响。在24和48小时后,使用发色甲基噻唑四唑溴化铵(MTT)染料评估细胞增殖。通过伤口测定研究细胞迁移。结果:在化学低氧条件下,Beclin-1和LC3的水平增加,这种变化可以被3-MA抑制。与对照组相比,用CoCl2处理24和48 h的细胞的细胞活力降低,并且用3-MA预处理可以稍微促进CoCl2抑制的细胞增殖。与对照组相比,用CoCl2处理24小时和48小时的细胞的细胞迁移和管形成增加。结论3-MA预处理可明显抑制CoCl2诱导的细胞迁移和管形成。结论:缺氧诱导的自噬降低了细胞活力,增加了RF / 6A细胞的迁移和管形成。 3-MA可以抑制体外低氧诱导的RF / 6A细胞的血管生成。本研究表明自噬在视网膜和脉络膜血管生成中起作用,并且自噬抑制剂可能是治疗脉络膜或视网膜新血管形成的潜在候选者。

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