1. 中山大学中山眼科中心//眼科学国家重点实验室,广东,广州,510060
2. 西安交通大学医学院第一附属医院,陕西,西安,710061
3. 美国俄克拉荷马大学医学院Harold Hamm糖尿病研究中心,俄克拉荷马OK 73104,USA
网络首发:2017-01-20,
纸质出版:2017
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钟毅敏, 李晶明, 张欣, 等. 转录因子X 盒结合蛋白1 参与视网膜色素上皮抗氧化 防御机制[J]. 中山大学学报(医学科学版), 2017,38(1).
ZHONG Yi-min, LI Jing-ming, ZHANG Xin, et al. Role of X-box Binding Protein 1 in Acrolein-induced Oxidative Injury of Retinal Pigment Epithelium[J]. Journal of Sun Yat-sen University (Medical Sciences), 2017, 38(1).
钟毅敏, 李晶明, 张欣, 等. 转录因子X 盒结合蛋白1 参与视网膜色素上皮抗氧化 防御机制[J]. 中山大学学报(医学科学版), 2017,38(1). DOI:
ZHONG Yi-min, LI Jing-ming, ZHANG Xin, et al. Role of X-box Binding Protein 1 in Acrolein-induced Oxidative Injury of Retinal Pigment Epithelium[J]. Journal of Sun Yat-sen University (Medical Sciences), 2017, 38(1). DOI:
摘要:【目的】视网膜色素上皮(RPE)的氧化损伤在年龄相关性黄斑变性(ARMD)的发病机制中起着核心作用。本 研究旨在探讨内质网应激及其重要的转录因子X盒结合蛋白1(XBP1)在丙烯醛引起的RPE氧化损伤中起到的作用,从而 为阐明ARMD的发病机制提供思路。【方法】用75 μmol/L丙烯醛分别处理人视网膜色素上皮细胞系(ARPE-19)2~24 h,观 察内质网应激蛋白葡萄糖调节蛋白78(GRP78)及XBP1的表达。用XBP1 siRNA转染细胞,下调XBP1蛋白水平,用Western blot检测抗氧化基因Nrf2、SOD2在蛋白水平的表达;用DCF染色观察细胞活性氧产物(ROS)的产生;用TUNEL染色观察细 胞凋亡改变。细胞用XBP1 siRNA或对照siRNA预处理后,加入丙烯醛,检测RPE细胞的凋亡情况。7只XBP1flox/flox小鼠,一 眼视网膜下注射Cre腺病毒,对侧眼视网膜下注射GFP腺病毒作对照。1周后取眼球。其中3只小鼠用TRIzol提取RPE的 RNA,用实时RT-PCR法,检测XBP1 的下游基因ERdj4和p58IPK在RNA水平的表达。另4只小鼠眼球作视网膜冰冻切片, 观察腺病毒在视网膜下腔的表达,用免疫荧光染色法检测XBP1 以及抗氧化基因Nrf2 和SOD2 在RPE 的表达。【结果】丙 烯醛分别处理RPE 细胞2 h 和4 h,GRP78 的表达明显增加。处理6 h XBP1 蛋白激活。XBP1 表达的下调伴有抗氧化基因 Nrf2和SOD2表达的减少,细胞内ROS的增加,并诱发细胞的凋亡。敲低XBP1以后丙烯醛对细胞的毒性作用明显增加。通 过视网膜下注射Cre腺病毒成功转染XBP1flox/flox小鼠RPE。与对照组相比,转染Cre腺病毒的小鼠RPE内的XBP1蛋白表达 明显减少,RPE 内的ERdj4 和p58IPK RNA 水平显著下调;抗氧化基因Nrf2 和SOD2 表达明显减少。【结论】丙烯醛作用于 RPE细胞,激活内质网应激以及转录因子XBP1。抑制XBP1引起RPE内抗氧化基因表达的减少,ROS的产生增加,并且增 加丙烯醛的细胞毒性。XBP1参与RPE细胞内抗氧化应激防御机制。
Abstract:【Objective】The oxidative injury of retinal pigment epithelium(RPE)plays a key role in the pathogenesis of agerelated macular degeneration(ARMD). This study is to investigate the effects of endoplasmic reticulum stress and the vital transcriptionalfactor X-box binding protein 1(XBP1)in acrolein-induced oxidative damage of RPE.【Methods】RPE cells were treated with acrolein (75 μmol/L)for 2 ~ 24 h,expression of glucose regulated protein 78(GRP78)and XBP1 was determined by Western blot analysis. After being transfected with XBP1 siRNA with 24 h,the expression of XBP1 was knocked-down in RPE cells. Protein level of Nrf2 and SOD2 was then determined by Western blot analysis and intracellular Reactive Oxygen Species(ROS)generation was determined by DCF staining. Acrolein was added for 8 h after being transfected with XBP1 siRNA or control siRNA for 24 h. Apoptosis was detected by TUNEL assay before and after the treatment. Subretinal injection of Cre or GFP adenovirus was performed in XBP1flox mice. After 1 week the mice were sacrificed. Total RNA was extracted from mice eyecups using TRIzol and real-time RT-PCR was performed to determine the two XBP1 down-stream genes,ERdj4 and p58IPK. Cryosectioning and immunofluorescent staining were performed to look at the expression of XBP1,Nrf2 and SOD2 in mice RPE.【Results】Protein level of GRP78 was significantly un-regulated after exposure to acrolein for 2 and 4 h. XBP1 was activated after acrolein treatment for 6 h. Knock-down of XBP1 by siRNA down-regu? lates anti-oxidant genes expression and increased ROS generation in RPE cells. Loss of XBP1 exacerbates acrolein-induced cell apoptosis. XBP1 was knocked-down in the RPE of XBP1flox mice after subretinal injection of Cre adenovirus. Decreased mRNA level of ERdj4 and p58IPK,and decreased Nrf2 and SOD2 expression were seen in the Cre-injected group.【Conclusions】Acrolein induces ER stress and activates XBP1 in RPE cells. Knock-down of XBP1 down-regulates anti-oxidant genes expression,increases ROS generation,and exacerbates acrolein-induced cell apoptosis. XBP1 plays a role in the anti-oxidant defense in the RPE cells.
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