| miR-133b靶向抑制SGTB对oxLDL诱导的血管内皮细胞损伤的影响* |
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| 引用本文： | 陈刚,陈九霖,吴俊. miR-133b靶向抑制SGTB对oxLDL诱导的血管内皮细胞损伤的影响*[J]. 中国应用生理学杂志, 2021, 37(6): 594-600. DOI: 10.12047/j.cjap.6111.2021.064 |
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| 作者姓名： | 陈刚 陈九霖 吴俊 |
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| 作者单位： | 黔西南州人民医院心血管内科, 贵州 黔西南州 562400 |
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| 摘 要： | 目的:探讨微小RNA-133b(miR-133b)靶向抑制富含谷氨酰胺三十四肽重复序列的小蛋白质分子(SGTB)对氧化低密度脂蛋白(oxLDL)诱导的血管内皮细胞损伤的影响。方法:采用100 μg/ml的oxLDL诱导人脐静脉血管内皮细胞(EVC-304)24 h构建血管内皮细胞损伤模型。将EVC-304细胞分为对照组、oxLDL组(oxLDL处理)、oxLDL+miR-NC组(转染20 nmol/L miR-NC+oxLDL处理)、oxLDL+miR-133b组(转染20 nmol/L miR-133b mimics+oxLDL处理)、oxLDL+si-NC组(转染20 nmol/L si-NC+oxLDL处理)、oxLDL+si-SGTB组(转染20 nmol/L si-SGTB+oxLDL处理)、oxLDL+miR-133b+pcDNA组(转染20 nmol/L si-SGTB和pcDNA+oxLDL处理)、oxLDL+miR-133b+pcDNA-SGTB组(转染20 nmol/L si-SGTB和pcDNA-SGTB处理)。实时荧光定量PCR(qRT-PCR)和蛋白质印记(Western blot)检测miR-133b和SGTB的表达水平;流式细胞术检测细胞凋亡;试剂盒检测丙二醛(MDA)含量、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的活性;Western blot检测B细胞淋巴瘤/白血病-2(Bcl-2)和Bcl-2相关X蛋白(Bax)的表达水平。双荧光素酶报告基因实验和Western blot验证miR-133b对SGTB的靶向调控关系。结果:与对照组比较,oxLDL诱导后EVC-304细胞miR-133b、Bcl-2的表达水平显著降低(P＜0.05),SGTB、Bax的表达水平显著升高(P＜0.05),MDA含量和细胞凋亡率显著增加(P＜0.05),SOD和GSH-Px活性显著降低(P＜0.05)。过表达miR-133b或干扰SGTB均可抑制oxLDL诱导的EVC-304细胞凋亡和氧化应激损伤(P＜ 0.05)。miR-133b与SGTB直接结合,过表达miR-133b显著下调SGTB表达(P＜0.05),抑制miR-133b显著上调SGTB表达(P＜0.05)。过表达SGTB可逆转过表达miR-133b对oxLDL诱导的血管内皮细胞损伤的影响(P＜0.05)。结论:miR-133b通过靶向抑制SGTB的表达,可减轻oxLDL诱导的血管内皮细胞氧化应激损伤和细胞凋亡。
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| 关 键 词： | 微小RNA-133b 富含谷氨酰胺三十四肽重复序列的小蛋白质分子 氧化低密度脂蛋白 血管内皮细胞 凋亡 氧化应激损伤 |
| 收稿时间： | 2020-06-09 |
Effects of miR-133b on oxLDL-induced vascular endothelial cell injury by targeting SGTB |
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| CHEN Gang,CHEN Jiu-lin,WU Jun. Effects of miR-133b on oxLDL-induced vascular endothelial cell injury by targeting SGTB[J]. Chinese journal of applied physiology, 2021, 37(6): 594-600. DOI: 10.12047/j.cjap.6111.2021.064 |
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| Authors: | CHEN Gang CHEN Jiu-lin WU Jun |
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| Affiliation: | Department of Internal Medicine-Cardiovascular, Qian Xi Nan People's Hospital, Guizhou 562400, China |
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| Abstract: | Objective: To investigate the effect of microRNA-133b (miR-133b) on oxidized low density lipoprotein (oxLDL) induced vascular endothelial cell injury by targeting small protein molecules rich in glutamine 34-tetrapeptide repeats (SGTB). Methods: Human umbilical vein endothelial cells (EVC-304) were induced by 100 μg/ml oxLDL for 24 h to construct a vascular endothelial cell injury model. EVC-304 cells were divided into control group, oxLDL group (oxLDL treatment), oxLDL+miR-NC group (transfectted with 20 nmol/L miR-NC+oxLDL treatment), oxLDL+miR-133b group (transfectted with 20 nmol/L miR-133b mimics +oxLDL treatment), oxLDL+si-NC group (transfectted with 20 nmol/L si-NC+oxLDL treatment), oxLDL+si-SGTB group (transfected with 20 nmol/L si-SGTB+oxLDL treatment), oxLDL+miR-133b+ pcDNA group (transfected with 20 nmol/L si-SGTB and pcDNA+oxLDL), oxLDL+miR-133b+pcDNA-SGTB group (transfected with 20 nmol/L si-SGTB and pcDNA-SGTB), 9 wells in each group. Real-time quantitative PCR (qRT-PCR) and Western blot were used to detect the expression levels of miR-133b and SGTB; flow cytometry was used to detect cell apoptosis; kits were used to detect malondialdehyde (MDA) content and the activities of superoxide disproportionation enzyme (SOD) and glutathione peroxidase (GSH-Px). The expression levels of Bcl-2 and Bax protein were detected by Western blot. The dual luciferase reporter gene assay and Western blot were used to verify the targeted and regulatory between miR-133b and SGTB. Results: Compared with the control group, the expressions of miR-133b and Bcl-2 in EVC-304 cells were decreased significantly after oxLDL induction, while the expression levels of SGTB and Bax were sincreased ignificantly (P＜0.05), the MDA content and apoptosis rate were increased significantly (P＜0.05), and the activities of SOD and GSH-Px were decreased significantly (P＜0.05). Over-expression of miR-133b or interfering with SGTB inhibited oxLDL-induced apoptosis and oxidative stress in EVC-304 cells (P＜ 0.05). miR-133b directly bound to SGTB, miR-133b overexpression significantly down-regulated SGTB expression (P＜0.05), miR-133b inhibition significantly up-regulated SGTB expression (P＜0.05) Over-expression of SGTB reversed the effect of over-expressing miR-133b on oxLDL-induced vascular endothelial cell injury (P＜0.05). Conclusion: miR-133b could attenuate oxidative stress damage and apoptosis induced by oxLDL in vascular endothelial cells by targeting and inhibiting SGTB expression. |
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| Keywords: | microRNA-133b small protein molecules rich in glutamine 34-tetrapeptide repeats oxidized low density lipoprotein vascular endothelial cells apoptosis oxidative stress injury |
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