北京大学学报(医学版) ›› 2020, Vol. 52 ›› Issue (6): 1082-1087. doi: 10.19723/j.issn.1671-167X.2020.06.015

• 论著 • 上一篇    下一篇

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

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:2018-12-13 出版日期:2020-12-18 发布日期:2020-12-13
  • 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(J2017Z608);首都医科大学附属北京世纪坛医院青年基金(2017-q27);中心实验室开放课题(2019-KF28)

Association between CMTM5 gene and coronary artery disease and the relative mechanism

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

  1. Department of Cardiology, Beijing Shijitan Hospital of Capital Medical University, Beijing 100034, China
  • Received:2018-12-13 Online:2020-12-18 Published:2020-12-13
  • Contact: Jian-jun PENG E-mail:pjj1972@sina.com
  • Supported by:
    Foundation of Research and Development Plan of China Railway Corporation(J2017Z608);Youth Foundation(2017-q27);Open Research Funding of Central Laboratory of Beijing Shijitan Hospital Affiliated to the Capital Medical University(2019-KF28)

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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 5,CMTM5)基因与冠状动脉粥样硬化性心脏病(简称冠心病)发生风险的相关性,及CMTM5基因表达变化对THP-1细胞黏附及迁移能力的影响。方法:采用病例对照研究法,入选700例首都医科大学附属北京世纪坛医院心血管内科的住院患者,采用冠状动脉造影法,将结果提示至少存在一支血管内径狭窄≥50%的患者诊断为冠心病。采用逆转录-聚合酶链反应法(reverse transcription-polymerase chain reaction,RT-PCR)测定CMTM5基因表达,酶联免疫吸附测定法(enzyme linked immunosorbent assay,ELISA)检测入选患者血浆CMTM5水平,Logistic回归方法分析CMTM5基因与冠心病发生风险的相关性。培养人血管内皮细胞(endothelial cells,ECs)及THP-1细胞,采用黏附实验及Transwells迁移实验评价CMTM5基因对THP-1趋化能力的影响。结果:冠心病组患者CMTM5基因mRNA表达量是对照组表达量的3.45倍,明显高于对照组(P<0.05)。冠心病组血浆CMTM5蛋白平均水平为(206.1±26.9) μg/L,明显高于对照组的(125.3±15.2) μg/L(P<0.05)。Logistic回归分析纳入年龄、性别、体重指数、吸烟、高血压、糖尿病、高脂血症等冠心病的易患因素和CMTM5基因,结果提示,CMTM5基因仍与冠心病的发生风险存在显著相关性(P<0.05)。黏附实验及Transwells实验结果均提示,过表达CMTM5 ECs组(EO组)中,THP-1细胞的黏附数量及迁移数量明显高于过表达CMTM5对照组(EO-MOCK组)、正常ECs组(EN组)、低表达CMTM5对照组(ES-MOCK组)和低表达CMTM5 ECs组(ES组), 相反,ES组中THP-1细胞黏附数量及迁移数量明显低于其他4组,差异均有统计学意义(P均<0.01)。结论:CMTM5基因与冠心病的发生发展密切相关,CMTM5基因过表达促进THP-1黏附及迁移能力,从而促进动脉粥样硬化和冠心病的发生发展。

关键词: 动脉粥样硬化, 冠状动脉粥样硬化性心脏病, 趋化素样因子超家族成员5, 基因

Abstract:

Objective: To elucidate the correlation between CKLF-like MARVEL transmembrane domain containing member 5 (CMTM5) gene and the risk of coronary artery disease (CAD), and to detect the effects of CMTM5 gene expression changes on the ability of adhesion and migration of THP-1 cells. Methods: Using case-control method, a total of 700 hospitalized patients in Shijitan Hospital were enrolled in this study. CAD were diagnosed by coronary angiography, which was defined as at least one blood vessel diameter stenosis ≥50% according to the result of coronary angiography. Reverse transcription-polymerase chain reaction (RT-PCR) method was used to detect CMTM5 gene expression; enzyme linked immunosorbent assay (ELISA) method to detect the plasma level of CMTM5; and Logistic regression to analyze CMTM5 genes and the risk of CAD. Human vascular endothelial cells (ECs) and THP-1 cells were cultivated, adhesion and Transwells experiments were used to evaluate the chemotactic capabi-lity of CMTM5 gene on THP-1 cells. Results: In this study, 350 CAD patients matched with 350 control patients were included. RT-PCR results revealed CMTM5 mRNA expression in CAD group was 3.45 times compared with control group, which was significantly higher than that in control group (P<0.05). The levels of CMTM5 plasma protein in CAD group was (206.1±26.9) μg/L, which was significantly higher than that in control group (125.3±15.2) μg/L (P<0.05). After adjusted for the risk factors of age, gender, BMI, smoking, hypertension, diabetes and hyperlipidemia, Logistic regression analysis results indicated that CMTM5 was the susceptibility factors of CAD, which still had significant correlation with CAD (P<0.05). Adhesion and Transwells experiments results revealed that the numbers of adhesion and migration of THP-1 cells in CMTM5 overexpression ECs group (EO group) were significantly higher than that in lenti-mock infected ECs group (EO-MOCK group), non-infected ECs group (EN group), lenti-mock infected ECs group (ES-MOCK group), and CMTM5 suppression ECs group (ES group). On the contrary, the numbers of adhesion and migration of THP-1 cells in ES group were significantly lower than that in the other four groups (P<0.01). Conclusion: CMTM5 gene was closely related to the development of CAD. CMTM5 overexpression promoted the adhesion and migration of THP-1, which might play a part in the mechanisms of atherosclerosis and CAD.

Key words: Atherosclerosis, Coronary artery disease, CMTM5, Gene

中图分类号: 

  • R543.3

表1

CAD组和对照组的临床基线资料"

Variables Control group (n=350) CAD group (n=350) P
Age/years, x-±s 58.2±7.3 58.7±8.2 0.535
Gender/(male/female), n 200/150 200/150 Match
BMI/(kg/m2), x-±s 25.0±4.0 25.3±5.3 0.525
DM, n (%) 32 (9.1) 79 (22.6) <0.001*
Hypertension, n (%) 185 (52.9) 220 (62.9) 0.013*
Current smoking, n (%) 115 (32.9) 170 (48.6) <0.001*
TG/(mmol/L), x-±s 2.15±1.02 2.24±1.30 0.002*
TC/(mmol/L), x-±s 4.72±1.05 5.03±1.61 <0.001*
LDL-C/(mmol/L), x-±s 2.52±0.62 2.63±0.83 0.013*
HDL-C/(mmol/L), x-±s 1.41±0.44 1.44±0.53 0.286

图1

CMTM5 mRNA和血浆蛋白水平在冠心病组和对照组之间的表达"

表2

Logistic回归分析冠心病的易感因素"

Risk factors B SE OR 95%CI P
Lower Upper
Age -0.960 0.116 0.383 0.305 0.481 <0.001
Gender 0.567 0.067 1.763 1.546 2.010 <0.001
BMI -0.007 0.008 0.993 0.976 0.971 0.377
Smoking -0.822 0.070 0.439 0.383 0.504 <0.001
Hypertension 0.350 0.066 1.420 1.247 1.617 <0.001
Diabetes mellitus 0.579 0.052 1.784 1.611 1.975 <0.001
Hyperlipidemia 0.259 0.070 1.296 1.130 1.487 <0.001
CMTM5 -0.044 0.007 0.957 0.943 0.971 0.002

图2

CMTM5基因表达量变化对THP-1黏附能力的影响(荧光染色 ×4)"

图3

CMTM5基因表达量变化对THP-1迁移能力的影响(吉姆萨染色 ×10)"

[1] Hansson GK. Inflammation, atherosclerosis, and coronary artery disease[J]. N Engl J Med, 2005,352(16):1685-1695.
doi: 10.1056/NEJMra043430 pmid: 15843671
[2] Weber C, Noels H. Atherosclerosis: current pathogenesis and therapeutic options[J]. Nat Med, 2011,17(11):1410-1422.
doi: 10.1038/nm.2538 pmid: 22064431
[3] Aikawa M, Libby P. The vulnerable atherosclerotic plaque: pathogenesis and therapeutic approach[J]. Cardiovasc Pathol, 2004,13(3):125-138.
pmid: 15081469
[4] Koenen RR, Weber C. Chemokines: established and novel targets in atherosclerosis[J]. EMBO Mol Med, 2011,3(12):713-725.
doi: 10.1002/emmm.201100183
[5] Braunersreuther V, Mach F, Steffens S. The specific role of chemokines in atherosclerosis[J]. Thromb Haemost, 2007,97(5):714-721.
pmid: 17479181
[6] Zernecke A, Shagdarsuren E, Weber C. Chemokines in atherosclerosis: an update[J]. Arterioscler Thromb Vasc Biol, 2008,28(11):1897-1908.
doi: 10.1161/ATVBAHA.107.161174 pmid: 18566299
[7] Aukrust P, Halvorsen B, Yndestad A, et al. Chemokines and cardiovascular risk[J]. Arterioscler Thromb Vasc Biol, 2008,28(11):1909-1919.
doi: 10.1161/ATVBAHA.107.161240 pmid: 18669888
[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.
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] 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.1671-167X.2015.06.003
[11] Charo IF, Ransohoff RM. The many roles of chemokines and chemokine receptors in inflammation[J]. N Engl J Med, 2006,354(6):610-621.
doi: 10.1056/NEJMra052723 pmid: 16467548
[12] Heydtmann M, Adams DH. Chemokines in the immunopathogenesis of hepatitis C infection[J]. Hepatology, 2009,49(2):676-688.
doi: 10.1002/hep.22763 pmid: 19177577
[13] Golay J, Introna M. Chemokines and antagonists in non-Hodgkin’s lymphoma[J]. Expert Opin Ther Targets, 2008,12(5):621-635.
doi: 10.1517/14728222.12.5.621 pmid: 18410244
[14] Tiemessen CT, Kuhn L. CC chemokines and protective immunity: insights gained from mother-to-child transmission of HIV[J]. Nat Immunol, 2007,8(3):219-222.
doi: 10.1038/ni0307-219 pmid: 17304227
[15] Dhami H, Fritz CE, Gankin B, et al. The chemokine system and CCR5 antagonists: potential in HIV treatment and other novel therapies[J]. J Clin Pharm Ther, 2009,34(2):147-160.
doi: 10.1111/j.1365-2710.2008.00978.x pmid: 19250135
[16] Lundberg GA, Kellin A, Samnegard A, et al. Severity of coronary artery stenosis is associated with a polymorphism in the CXCL16/SR-PSOX gene[J]. J Intern Med, 2005,257(5):415-422.
doi: 10.1111/j.1365-2796.2005.01469.x pmid: 15836657
[17] Singh N, Rai H, Sinha N, et al. Association of V249I and T280M polymorphisms in the chemokine receptor CX3CR1 gene with early onset of coronary artery disease among North Indians[J]. Genet Test Mol Biomarkers, 2012,16(7):756-760.
doi: 10.1089/gtmb.2011.0256 pmid: 22731642
[18] Cai W, Tao J, Zhang X, et al. Contribution of homeostatic chemokines CCL19 and CCL21 and their receptor CCR7 to coronary artery disease[J]. Arterioscler Thromb Vasc Biol, 2014,34(9):1933-1941.
pmid: 24990231
[19] Zhang JW, Liu TF, Chen XH, et al. Validation of aspirin response-related transcripts in patients with coronary artery disease and preliminary investigation on CMTM5 function[J]. Gene, 2017,624:56-65.
doi: 10.1016/j.gene.2017.04.041
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