北京大学学报(医学版) ›› 2020, Vol. 52 ›› Issue (5): 856-862. doi: 10.19723/j.issn.1671-167X.2020.05.010

• 论著 • 上一篇    下一篇

CMTM5基因与冠心病患者支架内再狭窄发生风险

刘滕飞,林涛,任利辉,李广平,彭建军()   

  1. 首都医科大学附属北京世纪坛医院心血管内科,北京 100034
  • 收稿日期:2018-11-15 出版日期:2020-10-18 发布日期:2020-10-15
  • 通讯作者: 彭建军 E-mail:pjj1972@sina.com
  • 基金资助:
    中国铁路总公司科技研究开发计划课题(J2017Z608);首都医科大学附属北京世纪坛医院院青年基金(2017-q27);首都医科大学附属北京世纪坛医院中心实验室开放课题(2019-KF28)

Association of CMTM5 gene expression with the risk of in-stent restenosis in patients with coronary artery disease after drug-eluting stent implantation and the effects and mechanisms of CMTM5 on human vascular endothelial cells

Teng-fei LIU,Tao LIN,Li-hui REN,Guang-ping LI,Jian-jun PENG()   

  1. Department of Cardiology, Shijitan Hospital, Beijing 100034, China
  • Received:2018-11-15 Online:2020-10-18 Published:2020-10-15
  • Contact: Jian-jun PENG E-mail:pjj1972@sina.com
  • Supported by:
    Foundation of Research and Development Plan of China Railway Corporation(J2017Z608);Youth Foundation of Central Laboratory of Beijing Shijitan Hospital Affiliated to the Capital Medical University(2017-q27);Open Research Funding of Central Laboratory of Beijing Shijitan Hospital Affiliated to the Capital Medical University(2019-KF28)

RICH HTML

  

摘要:

目的:探讨趋化素样因子超家族成员5 (CKLF-like marvel transmembrane domain containing member, CMTM5)基因与冠心病患者支架内再狭窄(in-stent restenosis, ISR)发生风险及该基因对人血管内皮细胞(endothelial cells, ECs)增殖和迁移作用及其机制。方法: 选择2015年1月至2016年12月在首都医科大学附属北京世纪坛医院心血管内科接受住院治疗并行经皮冠状动脉介入治疗手术的冠心病患者,共计124例,采用光学比浊法测定血小板聚集率并进行血小板高反应性分组;冠脉造影术明确患者支架内再狭窄发生;RT-PCR法测定CMTM5基因表达;构建CMTM5基因过表达、敲减及对照组内皮细胞系,采用细胞计数法、MTT法、Brdu掺入实验和流式细胞术检测ECs增殖能力,刮伤和Transwell实验检测ECs迁移能力,Western-blot检测信号通路表达。结果: CMTM5基因在血小板高反应性(high on aspirin platelet reactivity,HAPR)组表达量为非血小板高反应性(no-high on aspirin platelet reactivity,No-HAPR)组表达量的1.72倍(P<0.05)。HAPR组ISR发生率为25.8%(8例), No-HAPR组ISR发生率为 9.7%(9例), HAPR组患者ISR的发生率高于No-HAPR组的发生率(P=0.04,OR=2.95,95%CI:1.16~7.52),表明该基因与冠心病患者支架术后支架内再狭窄发生风险显著相关(P<0.05)。CMTM5基因过表达抑制ECs增殖和迁移能力(P<0.05), PI3K/Akt信号通路参与该基因对内皮细胞增殖和迁移调控作用。结论:CMTM5基因与冠心病患者支架内再狭窄事件发生风险可能存在相关性,CMTM5基因通过PI3K/Akt信号通路参与调控ECs增殖和迁移。

关键词: 趋化素样因子超家族成员5, 内皮细胞, 血小板反应性, 心血管事件

Abstract:

Objective: To elucidate the correlation between CKLF-like marvel transmembrane domain containing member (CMTM5) gene and the risk of in-stent restenosis (ISR) with coronary artery disease (CAD) patients and to detect the effects and mechanisms of CMTM5-stimulated genes on human vascular endothelial cells (ECs) proliferation and migration. Methods: A total of 124 hospitalized patients in Shijitan Hospital were enrolled in this study. All the CAD patients were detected with platelet reactivity and grouped into two groups according to platelet reactivity; ISR was conformed by coronary angiography; RT-PCR method was used to detect CMTM5 gene expression; The CMTM5 over expression, reduction and control EC lines were established; Cell count, MTT, Brdu and flow cytometry methods were used to detect the proliferation of ECs, scratch and transwell experiments to test the migration of ECs, Western blot was used to detect signal path expressions. Results: CMTM5 gene expression in HAPR (High on aspirin platelet reactivity) group was 1.72 times compared with No-HAPR group, which was significantly higher than No-HAPR group. HAPR group ISR rate was 25.8% (8 cases), the incidence of No-HAPR ISR group was 9.7% (9 cases), and the results showed that in HAPR group, the incidence of ISR was significantly higher than that in No-HAPR group (P=0.04, OR=0.04, 95%CI=1.16-7.52), which showed that CMTM5 gene was significantly correlated with the risk of ISR. In HAPR group ISR rate was 25.8% (8 cases), the incidence of ISR in No-HAPR group was 9.7% (9 cases), and the results showed that the risk of ISR in HAPR group was significantly higher than that in No-HAPR group. All the results showed that CMTM5 was significantly correlated with the risk of ISR in CAD patients (P<0.05). CMTM5 overexpression inhibited the proliferation and migration ability of ECs (P<0.05), PI3K/Akt signaling pathways were involved in the role of regulation on ECs. Conclusion: Our results revealed that CMTM5 gene was closely related with ISR, CMTM5 overexpression may repress ECs proliferation and migration through regulating PI3K-Akt signaling.

Key words: Platelet reactivity, CKLF-like marvel transmembrane dimain containing member 5, Coronary artery diseases, In-stent restenosis

中图分类号: 

  • R543.3

表1

HAPR组和No-HAPR组的临床基线资料"

Variables HAPR(n=31) No-HAPR(n=93) P
Age/years, x-±s 76.3±7.3 74.8±8.9 0.063
Male, n(%) 27(87.1) 72(77.4) 0.308
BMI/(kg/m2), x-±s 26.1±3.3 24.5±3.1 0.451
Hypertension, n(%) 25(80.6) 66(71.0) 0.354
Diabetes, n(%) 12(38.7) 32(34.4) 0.670
Current smoking, n(%) 11(35.5) 15(16.1) 0.039*
Hyperlipidemia, n(%) 27(87.1) 75(80.6) 0.589
Essential medicines, n(%) 14(45.2) 55(59.1) 0.212
ACEI/ARB 22(70.9) 61(65.6) 0.663
β-blocker 12(38.7) 45(48.4) 0.408
CCB 13(41.9) 31(33.3) 0.395
Nitrates 24(77.4) 81(87.1) 0.249
Stains 27(87.1) 72(77.4) 0.308
Cardiovascular events, n(%) 8 (25.8) 9 (9.7) 0.037

表2

COX回归分析影响心血管事件发生的危险因素"

Risk factors HR 95%CI P
ΔCt CMTM5 0.086 0.053-0.099 0.010
Current smoking 1.998 1.050-3.802 0.035

图1

CMTM5过表达抑制血管内皮细胞增殖能力"

图2

CMTM5低表达促进血管内皮细胞增殖能力"

图3

CMTM5基因对人血管内皮细胞横向迁移能力的影响"

图4

Transwell实验-观察CMTM5 对血管内皮细胞纵向迁移能力影响"

图5

Western blot检测信号通路蛋白的表达"

[1] Kokkinidis DG, Waldo SW, Armstrong EJ. Treatment of coronary artery in-stent restenosis[J]. Expert Rev Cardiovasc Ther, 2017,15(3):191-202.
doi: 10.1080/14779072.2017.1284588 pmid: 28116914
[2] Kuchulakanti PK, Chu WW, Torguson R, et al. Correlates and long-term outcomes of angiographically proven stent thrombosis with sirolimus- and paclitaxel-eluting stents[J]. Circulation, 2006,113(8):1108-1113.
doi: 10.1161/CIRCULATIONAHA.105.600155 pmid: 16490815
[3] Philip F. Duration of triple therapy in patients requiring oral anticoagulation after drug-eluting stent implantation[J]. J Am Coll Cardiol, 2015,66(9):1088-1089.
pmid: 26314542
[4] Byrne RA, Joner M, Kastrati A. Stent thrombosis and restenosis: what have we learned and where are we going? The andreas gruntzig lecture ESC 2014[J]. Eur Heart J, 2015,36(47):3320-3331.
doi: 10.1093/eurheartj/ehv511 pmid: 26417060
[5] Moliterno DJ. Healing achilles: sirolimus versus paclitaxel[J]. N Engl J Med, 2005,353(7):724-727.
doi: 10.1056/NEJMe058140 pmid: 16105991
[6] Virmani R, Farb A. Pathology of in-stent restenosis[J]. Curr Opin Lipidol, 1999,10(6):499-506.
doi: 10.1097/00041433-199912000-00004 pmid: 10680043
[7] Ma X, Hibbert B, McNulty M, et al. Heat shock protein 27 attenuates neointima formation and accelerates reendothelialization after arterial injury and stent implantation: importance of vascular endothelial growth factor up-regulation[J]. FASEB J, 2014,28(2):594-602.
doi: 10.1096/fj.13-230417
[8] Li H, Guo X, Shao L, et al. CMTM5-v1, a four-transmembrane protein, presents a secreted form released via a vesicle-mediated secretory pathway[J]. BMB Rep, 2010,43(3):182-187.
doi: 10.5483/bmbrep.2010.43.3.182 pmid: 20356458
[9] Voora D, Cyr D, Lucas J, et al. Aspirin exposure reveals novel genes associated with platelet function and cardiovascular events[J]. J Am Coll Cardiol, 2013,62(14):1267-1276.
doi: 10.1016/j.jacc.2013.05.073 pmid: 23831034
[10] Liu TF, Zhang JW, Chen XH, et al. Comparison between urinary 11-dehydrothromboxane B2 detection and platelet light transmission aggregometry (LTA) assays for evaluating aspirin response in elderly patients with coronary artery disease[J]. Gene, 2015,571(1):23-27.
doi: 10.1016/j.gene.2015.06.045 pmid: 26095809
[11] 刘滕飞, 张婧薇, 陈夏欢, 等. CMTM5基因rs723840单核苷酸多态性与阿司匹林治疗下血小板高反应性的相关性研究[J]. 北京大学学报(医学版), 2015,47(6):905-909.
doi: 10.3969/j.issn.1671167X.2015.06.003
[12] Teirstein P, Reilly JP. Late stent thrombosis in brachytherapy: the role of long-term antiplatelet therapy[J]. J Invasive Cardiol, 2002,14(3):109-114.
pmid: 11870263
[13] Schmieder RE. Endothelial dysfunction: how can one intervene at the beginning of the cardiovascular continuum[J]. J Hypertens Suppl, 2006,24(Suppl 2):S31-35.
[14] Xiao Y, Yuan Y, Zhang Y, et al. CMTM5 is reduced in prostate cancer and inhibits cancer cell growth in vitro and in vivo[J]. Clin Transl Oncol, 2015,17(6):431-437.
doi: 10.1007/s12094-014-1253-z pmid: 25387568
[1] 罗靓,李云,王红彦,相晓红,赵静,孙峰,张晓盈,贾汝琳,李春. 抗内皮细胞抗体检测在早期流产中的预测价值[J]. 北京大学学报(医学版), 2023, 55(6): 1039-1044.
[2] 顾阳阳,谭晓辉,宋文鹏,方冬,宋卫东,袁亦铭,冯宁翰,关瑞礼. 4′-甲基醚金连木黄酮对棕榈酸诱导的大鼠阴茎海绵体内皮细胞功能障碍的影响[J]. 北京大学学报(医学版), 2022, 54(4): 599-604.
[3] 申杰, 杨迪, 陈梦圆, 郭新彪. 长度和化学修饰在多壁碳纳米管诱导内皮细胞活化中的作用[J]. 北京大学学报(医学版), 2021, 53(3): 439-446.
[4] 黄丽东,宫玮玉,董艳梅. 生物活性玻璃对人脐静脉血管内皮细胞增殖及成血管的作用[J]. 北京大学学报(医学版), 2021, 53(2): 371-377.
[5] 刘滕飞,林涛,任利辉,李广平,彭建军. CMTM5基因与冠状动脉粥样硬化性心脏病的关联研究及机制探讨[J]. 北京大学学报(医学版), 2020, 52(6): 1082-1087.
[6] 谢静,赵玉鸣,饶南荃,汪晓彤,方滕姣子,李晓霞,翟越,李静芝,葛立宏,王媛媛. 3种口腔颌面部来源的间充质干细胞成血管内皮分化潜能的比较研究[J]. 北京大学学报(医学版), 2019, 51(5): 900-906.
[7] 张静,李素芳,陈红,宋俊贤. miR-106b-5p在调节内皮细胞基因表达谱中的作用[J]. 北京大学学报(医学版), 2019, 51(2): 221-227.
[8] 刘颖君,欧阳翔英,王宇光,吕培军,安娜. 生长停滞特异性蛋白6在牙龈卟啉单胞菌脂多糖诱导内皮细胞黏附因子及趋化因子表达中的作用[J]. 北京大学学报(医学版), 2018, 50(1): 20-25.
[9] 梁乃文,石磊,黄颖,邓旭亮. 不同形貌纯钛表面对人脐静脉内皮细胞生物学行为的影响[J]. 北京大学学报(医学版), 2017, 49(1): 43-048.
[10] 李蓬1,万蒙2,刘健如2,李良忠1,张大鹍3△. 过氧化物酶体增生物激活受体γ在牙龈卟啉单胞菌刺激血管内皮细胞氧化应激中的作用[J]. 北京大学学报(医学版), 2015, 47(6): 977-982.
[11] 高倩,彭清,陈靖,张巍,王朝霞,袁云,左越焕,刘靖. 法布里病的在体血管功能评价[J]. 北京大学学报(医学版), 2015, 47(5): 796-799.
[12] 吴迪, 欧阳翔英, 万蒙. 牙龈卟啉单胞菌感染内皮细胞导致白介素-8表达升高的胞内机制初探[J]. 北京大学学报(医学版), 2014, 46(2): 278-283.
[13] 陈鑫磊, 边曦, 秦泽莲. Periostin在酸性环境下对人脐静脉内皮细胞功能的影响[J]. 北京大学学报(医学版), 2011, 43(6): 855-860.
[14] 杨玲玲, 邵珲, 原鹏波, 郭晓玥, 张小为, 赵扬玉. 缺氧诱导因子-1α及其靶基因在双胎输血综合征胎盘组织中的表达[J]. 北京大学学报(医学版), 2011, 43(6): 792-797.
[15] 刘涛, 覃新程, 李维仁, 周峰, 李广永, 辛华, 巩艳青, 辛钟成. 淫羊藿苷和淫羊藿次苷Ⅱ对内皮细胞eNOS表达和NOS活性的影响[J]. 北京大学学报(医学版), 2011, 43(4): 500-504.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!