文章摘要
王玉风,付珂,王洪亮.藏红花素通过跨膜受体蛋白 /发状分裂相关增强子 1信号通路对缺氧诱导的视网膜神经节细胞凋亡的影响[J].安徽医药,2024,28(1):193-197.
藏红花素通过跨膜受体蛋白 /发状分裂相关增强子 1信号通路对缺氧诱导的视网膜神经节细胞凋亡的影响
Effects of crocin on hypoxia-induced retinal ganglion cell apoptosis via the transmembrane receptor protein/hairy division-related enhancer 1 signaling pathway
  
DOI:10.3969/j.issn.1009-6469.2024.01.041
中文关键词: 番红花  细胞低氧  基因, bcl-2  藏红花素  视网膜神经节细胞  细胞凋亡  跨膜受体蛋白 Notch1  发状分裂相关增强子 1  大鼠, Sprague-Dawley
英文关键词: Crocus  Cell hypoxia  Genes,bcl-2  Saffron  Retinal ganglion cells  Apoptosis  Transmembrane receptor protein Notch1  Hairy division related enhancer 1  Rats, Sprague-Dawley
基金项目:南阳市 2021年科技发展计划项目( KJGG155)
作者单位
王玉风 南阳医学高等专科学校第一附属医院眼科河南南阳 473000 
付珂 南阳医学高等专科学校第一附属医院眼科河南南阳 473000 
王洪亮 南阳医学高等专科学校第一附属医院眼科河南南阳 473000 
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中文摘要:
      目的探讨藏红花素对缺氧诱导的视网膜神经节细胞凋亡的作用及其可能机制。方法于 2021年 1月至 2022年 1月采用不同浓度藏红花素处理视网膜神经节细胞 RGC-5,四甲基噻唑蓝( MTT)法检测细胞存活情况并筛选合适浓度。培养 RGC-5细胞并用氯化钴( CoCl2)处理建立缺氧模型,分为缺氧组、藏红花素组、阳性对照(抗坏血酸)组和藏红花素 +跨膜受体蛋白信号通路抑制剂(DAPT)组,另设对照组。 Cell counting kit-8法检测细胞存活情况;采用流式细胞术检测细胞凋亡率;钙荧光探针( Flou-4)实验检测各组细胞钙离子水平;实时定量 PCR法检测跨膜受体蛋白( Notch1)、发状分裂相关增强子 1(Hes-1) mRNA表达情况;蛋白质印迹法检测凋亡蛋白 B细胞淋巴瘤因子 2(Bcl-2)、 Bcl-2相关蛋白( Bax)、钙依赖性蛋白酶家族 1(Cal- pain1)蛋白表达情况。结果藏红花素组细胞活力 0.83±0.08高于缺氧组 0.45±0.04,细胞凋亡率( 17.92±1.21)%低于缺氧组(51.82±5.36)%,钙离子水平 0.27±0.04低于缺氧组 0.76±0.05,差异有统计学意义( P<0.05);藏红花素 +DAPT组细胞活力 0.50±0.06低于藏红花素组 0.83±0.08,细胞凋亡率( 36.50±3.50)%高于藏红花素组( 17.92±1.21)%,钙离子水平 0.65±0.05高于藏红花素组 0.27±0.04,差异有统计学意义( P<0.05)。与缺氧组比较,藏红花素组 Bcl-2蛋白表达水平升高, Notch1、Hes-1mRNA表达、 Bax和 Calpain1蛋白表达水平降低( P<0.05)。与藏红花素组比较,藏红花素 +DAPT组 Bcl-2蛋白表达水平降低, Notch1、Hes1mRNA表达、 Bax和 Calpain1蛋白表达水平升高( P<0.05)。结论藏红花素对体外培养的缺氧 RGC-5细胞凋亡有一定的抑制作用,可能是通过抑制钙离子内流,阻滞 Notch1/Hes-1通路,提高细胞内抑凋亡蛋白 Bcl-2表达水平发挥作用。
英文摘要:
      Objective To investigate the effect of crocin on hypoxia-induced retinal ganglion cell apoptosis and its possible mecha- nism.Methods In this study, RGC-5 retinal ganglion cells were treated with different concentrations of crocin from January 2021 toJanuary 2022, and cell survival was detected by tetramethylthiazole blue (MTT) method and suitable concentrations were screened.RGC-5 cells were cultured and treated with cobalt chloride (CoCl2) to establish a hypoxia model. They were assigned into hypoxiagroup, crocin group, positive control (ascorbic acid) group and crocin + transmembrane receptor protein signal pathway inhibitor(DAPT) group, another control group was set up. Cell survival was detected by Cell counting kit-8 method; the apoptosis rate was detect- ed by flow cytometry; the level of Ca2+ was detected by Flou-4 experiment; the mRNA expressions of transmembrane receptor protein (Notch1) and hairy division related enhancer 1 (Hes-1) were detected by real-time quantitative PCR; the expressions of apoptotic pro- tein B-cell lymphoma factor 2 (Bcl-2), Bcl-2 related protein (Bax) and calcium dependent protease family 1 (Calpain1) were detected by Western blotting .Results The cell viability 0.83±0.08 in crocin group was higher than that in hypoxia group 0.45±0.04, the apoptosisrate (17.92±1.21) % was lower than that in hypoxia group (51.82±5.36) %, and the level of calcium ion 0.27±0.04 was lower than that inhypoxia group 0.76±0.05. The differences were statistically significant (P<0.05). The cell viability 0.50±0.06 in crocetin +DAPT groupwas lower than that in crocetin group 0.83±0.08, the apoptosis rate (36.50±3.50) % was higher than that in crocetin group (17.92±1.21) %, and the level of calcium ion 0.65±0.05 was higher than that in crocetin group 0.27±0.04, the differences were statistically signif-icant (P<0.05). Compared with hypoxia group, the expression level of Bcl-2 protein in crocetin group was increased, and the expression levels of Notch1, Hes-1 mRNA, Bax and Calpain1 protein were decreased (P<0.05). Compared with crocin group, the expression level of Bcl-2 protein in crocin +DAPT group was decreased, and the expression levels of Notch1, Hes-1 mRNA, Bax and Calpain1 protein were in- creased (P<0.05).Conclusion Saffron can inhibit the apoptosis of hypoxia RGC-5 cells in vitro, which may play a role by inhibiting calci- um influx, blocking the Notch1 / Hes-1 pathway and increasing the expression level of intracellular anti apoptotic protein Bcl-2.
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