解剖学报 ›› 2023, Vol. 54 ›› Issue (3): 319-327.doi: 10.16098/j.issn.0529-1356.2023.03.010

• 细胞和分子生物学 • 上一篇    下一篇

长链非编码RNA alpha-2-巨球蛋白反义RNA 1靶向微小RNA-106b-5p调控氧化型低密度脂蛋白诱导的人脑微血管内皮细胞损伤

李薇1* 王丽2 汪志华3 刘庆春1 韩荣胜4
  

  1. 1. 青海省第五人民医院神经内科,西宁810000; 2. 青海省第五人民医院内分泌科,西宁 810000;  3. 青海心脑血管病专科医院影像科,西宁 810012; 4. 青海省第五人民医院心内科,西宁 810000
  • 收稿日期:2021-01-28 修回日期:2022-05-09 出版日期:2023-06-06 发布日期:2023-06-06
  • 通讯作者: 李薇 E-mail:vks081@163.com

Long non-coding RNA alpha-2-macroglobulin antisense RNA 1 regulating oxidized low density lipoprotein-induced human brain microvascular endothelial cell damage by targeting microRNA-106b-5p

LI  Wei1*  WANG  Li2  WANG  Zhi-hua3  LIU  Qing-chun1  HAN  Rong-sheng4   

  1. 1.Department of Neurology, the Fifth People’s Hospital of Qinghai Province, Xining810000, China;  2.Department of Endocrinology, the Fifth People’s Hospital of Qinghai Province, Xining810000, China;  3.Department of Imaging, Qinghai Cardiovascular and Cerebrovascular Disease Hospital, Xining810012, China;  4.Department of Cardiology, the Fifth People’s Hospital of Qinghai Province, Xining810000, China
  • Received:2021-01-28 Revised:2022-05-09 Online:2023-06-06 Published:2023-06-06
  • Contact: LI Wei E-mail:vks081@163.com

摘要:

目的 探讨长链非编码RNA (lncRNA)alpha-2-巨球蛋白反义RNA 1(A2M-AS1)靶向微小RNA(miR)-106b-5p对氧化型低密度脂蛋白(ox-LDL)诱导的人脑微血管内皮细胞损伤的影响。  方法 用ox-LDL诱导人脑微血管内皮细胞设为ox-LDL组,正常培养细胞为对照(Ctrl)组;A2M-AS1过表达(pcDNA-A2M-AS1组)、空载体(pcDNA组)、miR-106b-5p抑制剂(anti-miR-106b-5p组)、阴性对照(anti-miR-NC组)、pcDNA-A2M-AS1与对照mimic NC(miR-NC组)、pcDNA-A2M-AS1与miR-106b-5p模拟物(miR-106b-5p mimics组)转染细胞后加ox-LDL处理,n=9;Real-time PCR检测A2M-AS1与miR-106b-5p表达;试剂盒检测丙二醛(MDA)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)水平;流式细胞术及TUNEL法检测细胞凋亡;双荧光素酶报告基因实验检测A2M-AS1与miR-106b-5p靶向关系;Western blotting检测Bcl-2和Bax蛋白表达量。  结果 与Ctrl组比较,ox-LDL组A2M-AS1表达水平、SOD和CAT活性、Bcl-2蛋白水平降低,miR-106b-5p表达水平、MDA水平、凋亡率、Bax蛋白水平升高(P<0.05);过表达A2M-AS1或干扰miR-106b-5p降低ox-LDL诱导细胞后MDA水平、凋亡率与Bax蛋白水平,升高SOD、CAT活性和Bcl-2蛋白水平(P<0.05);A2M-AS1靶向miR-106b-5p;上调miR-106b-5p逆转过表达lncRNA A2M-AS1对ox-LDL诱导的人脑微血管内皮细胞损伤的作用。  结论 A2M-AS1通过靶向miR-106b-5p减轻ox-LDL诱导的人脑微血管内皮细胞损伤。

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Abstract:

Objective To investigate the effect of long non-coding RNA(lncRNA) alpha-2-macroglobulin antisense RNA 1 (A2M-AS1) targeting microRNA (miR)-106b-5p on oxidized low-density lipoprotein (ox-LDL)-induced injury of human brain microvascular endothelial cells.   Methods Human brain microvascular endothelial cells (ox-LDL group) were induced by ox-LDL, normal cultured cells were control group (Ctrl); A2M-AS1 overexpression (pcDNA-A2M-AS1 group), empty vector (pcDNA group), miR-106b-5p inhibitor (anti-miR-106b-5p group), negative control (anti-miR-NC group), pcDNA-A2M-AS1 with control mimic NC (miR-NC group), pcDNA-A2M-AS1 with miR-106b-5p mimic (miR-106b-5p mimics group) were transfected into cells and treated with ox-LDL, n=9. Real-time PCR was used to detect the expression levels of A2M-AS1 and miR-106b-5p; Kits were used to detect malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT)); Flow cytometry and TUNEL detected apoptosis; Dual luciferase reporter gene assay detected A2M-AS1 and miR-106b-5p targeting; Western blotting detected Bcl-2 and Bax protein expression.   Results Compared with the Ctrl group, the expression level of A2M-AS1 in the ox-LDL group decreased, and the activity of SOD and CAT and the protein level of Bcl-2 decreased (P<0.05), while the expression level of miR-106b-5p and the level of MDA increased (P<0.05), and the rate of apoptosis and the protein level of Bax increased (P<0.05). Overexpressing A2M-AS1 or interfering with miR-106b-5p decreased the MDA level, apoptosis rate and Bax protein level after ox-LDL-induced cells, and increased SOD, CAT activity and Bcl-2 protein level (P<0.05). A2M-AS1 targeted miR-106b-5p; up-regulation of miR-106b-5p reversed the effect of overexpressed lncRNA A2M-AS1 on ox-LDL-induced injury of human brain microvascular endothelial cells (P<0.05).   Conclusion A2M-AS1 attenuates ox-LDL-induced injury of human brain microvascular endothelial cells by targeting miR-106b-5p.

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