Roles of miRNA-24 in regulating endothelial nitric oxide synthase expression and vascular endothelial cell proliferation

被引:30
作者
Zhang, Wenyu [1 ]
Yan, Limei [2 ]
Li, Yumei [1 ]
Chen, Wei [1 ]
Hu, Nan [1 ]
Wang, Hui [1 ]
Ou, Hesheng [1 ]
机构
[1] Guangxi Med Univ, Coll Pharm, Nanning 530021, Peoples R China
[2] Univ South China, Biochem Ctr, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA-24; Cell proliferation; Endothelial nitric oxide synthase; Sp1; MYOCARDIAL-INFARCTION; ANGIOGENESIS; MICRORNAS; INHIBITION; FIBROSIS; DISEASES; GENES;
D O I
10.1007/s11010-015-2418-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study is to investigate the effect of miRNA-24 on endothelial nitric oxide synthase (eNOS) expression and vascular endothelial cell proliferation. Constructed high expression miRNA-24 plasmids were introduced into human umbilical vein endothelial cells (HUVECs) by liposome. Cell numbers were counted by a Hemocytometer, and cell proliferation was detected by MTT assay. The expression levels of eNOS and specificity protein 1 (Sp1) at mRNA and protein levels were, respectively, examined by real-time PCR, immunohistochemistry, and Western blotting. Compared with the control group, endothelial cell proliferation in miRNA-24 group significantly decreased by 64.24 % (6.53 +/- 0.11 vs 18.26 +/- 0.45, P < 0.01). The expression of eNOS at mRNA and protein levels in miRNA-24 group decreased by 64.21 % (0.34 +/- 0.01 vs 0.95 +/- 0.02, P < 0.05) and 82.86 % (0.072 +/- 0.06 vs 0.42 +/- 0.06, P < 0.05), respectively. Meanwhile, the expression of Sp1 at mRNA and protein levels in miRNA-24 group decreased by 64.64 % (0.35 +/- 0.01 vs 0.99 +/- 0.03, P < 0.05) and 60.34 % (0.23 +/- 0.05 vs 0.58 +/- 0.07, P < 0.05), respectively. In anti-miRNA-24 group, endothelial cell proliferation decreased by 33.46 % compared with the control group (12.15 +/- 0.21 vs 18.26 +/- 0.45, P < 0.01), while it increased by 46.25 % compared with the miRNA-24 group (12.15 +/- 0.21 vs 6.53 +/- 0.11, P < 0.01). The expression of eNOS at mRNA and protein levels in anti-miRNA-24 group decreased by 44.21 % (0.53 +/- 0.04 vs 0.95 +/- 0.02, P < 0.05) and by 30.95 %(0.29 +/- 0.05 vs 0.42 +/- 0.06, P < 0.05) compared with the control group, while it increased by 35.84 % (0.53 +/- 0.04 vs 0.34 +/- 0.01, P < 0.05) and by 75.17 % (0.29 +/- 0.05 vs 0.072 +/- 0.06, P < 0.05) compared with miRNA-24 group. The expression of Sp1 at mRNA and protein levels in ant-miRNA-24 group decreased by 36.36 % (0.63 +/- 0.04 vs 0.99 +/- 0.03, P < 0.05) and by 22.41 % (0.45 +/- 0.06 vs 0.58 +/- 0.07, P < 0.05) compared with the control group, while it increased by 44.44 % (0.63 +/- 0.04 vs 0.35 +/- 0.01, P < 0.05) and by 48.88 % (0.45 +/- 0.06 vs 0.23 +/- 0.05, P < 0.05) compared with miRNA-24 group. HUVECs proliferation and eNOS expression are significantly inhibited by miRNA-24. Sp1, which is regulated by miRNA-24, might act as one of the important factors involved in eNOS gene expression.
引用
收藏
页码:281 / 289
页数:9
相关论文
共 26 条
  • [1] MicroRNA-132-mediated loss of p120RasGAP activates the endothelium to facilitate pathological angiogenesis
    Anand, Sudarshan
    Majeti, Bharat K.
    Acevedo, Lisette M.
    Murphy, Eric A.
    Mukthavaram, Rajesh
    Scheppke, Lea
    Huang, Miller
    Shields, David J.
    Lindquist, Jeffrey N.
    Lapinski, Philip E.
    King, Philip D.
    Weis, Sara M.
    Cheresh, David A.
    [J]. NATURE MEDICINE, 2010, 16 (08) : 909 - U109
  • [2] Endothelium-derived nitric oxide and vascular physiology and pathology
    Arnal, JF
    Dinh-Xuan, AT
    Pueyo, M
    Darblade, B
    Rami, J
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (8-9) : 1078 - 1087
  • [3] Endothelial damage and stem cell repair in atherosclerosis
    Bai, Xue
    Wang, Xian
    Xu, Qingbo
    [J]. VASCULAR PHARMACOLOGY, 2010, 52 (5-6) : 224 - 229
  • [4] microRNAs in diseases: from candidate to modifier genes
    Bandiera, S.
    Hatem, E.
    Lyonnet, S.
    Henrion-Caude, A.
    [J]. CLINICAL GENETICS, 2010, 77 (04) : 306 - 313
  • [5] Let-7 in Cardiovascular Diseases, Heart Development and Cardiovascular Differentiation from Stem Cells
    Bao, Mei-Hua
    Feng, Xing
    Zhang, Yi-Wen
    Lou, Xiao-Ya
    Cheng, Yu
    Zhou, Hong-Hao
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (11) : 23086 - 23102
  • [6] miR-363-5p regulates endothelial cell properties and their communication with hematopoietic precursor cells
    Costa, Ana
    Afonso, Joana
    Osorio, Catarina
    Gomes, Ana L.
    Caiado, Francisco
    Valente, Joana
    Aguiar, Sandra I.
    Pinto, Francisco
    Ramirez, Mario
    Dias, Sergio
    [J]. JOURNAL OF HEMATOLOGY & ONCOLOGY, 2013, 6
  • [7] A novel truncated form of eNOS associates with altered vascular function
    Galluccio, Elena
    Cassina, Laura
    Russo, Isabella
    Gelmini, Fabrizio
    Setola, Emanuela
    Rampoldi, Luca
    Citterio, Lorena
    Rossodivita, Alessandra
    Kamami, Mikel
    Colombo, Antonio
    Alfieri, Ottavio
    Carini, Marina
    Bosi, Emanuele
    Trovati, Mariella
    Piatti, PierMarco
    Monti, Lucilla D.
    Casari, Giorgio
    [J]. CARDIOVASCULAR RESEARCH, 2014, 101 (03) : 492 - 502
  • [8] Gene regulation by transcription factors and microRNAs
    Hobert, Oliver
    [J]. SCIENCE, 2008, 319 (5871) : 1785 - 1786
  • [9] eNOS, metabolic syndrome and cardiovascular disease
    Huang, Paul L.
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2009, 20 (06) : 295 - 302
  • [10] Roles of Cardiovascular Risk Factors in Endothelial Nitric Oxide Synthase Regulation: An Update
    Jamaluddin, Md Saha
    Liang, Zhengdong
    Lu, Jian-Ming
    Yao, Qizhi
    Chen, Changyi
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2014, 20 (22) : 3563 - 3578