The research progress of mechanism of microRNAs which regulated by shear stress on atherosclerosis
CSTR:
Author:
Affiliation:

1. Integrative Traditional Chinese and Western Medicine College, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China;2. Department of Pediatric, Affiliated Nanhua Hospital,University of South China, Hengyang, Hunan 421002,China;3. Medicine School, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China)

Clc Number:

R543.5

  • Article
  • | |
  • Metrics
  • |
  • Reference [30]
  • |
  • Related [20]
  • | | |
  • Comments
    Abstract:

    Atherosclerosis (As) is the main pathological basis of cardiovascular and cerebrovascular diseases, which seriously threatens human life and health. As occurs in abnormal shear stress sites, and microRNAs regulated by shear stress are called “shear stress sensitive microRNAs”. Shear stress-sensitive microRNAs are involved in many aspects of the pathogenesis of As. This review summarizes the recent advances in the mechanism of shear stress-sensitive microRNAs in the development and progression of As.

    Reference
    [1] Hansson GK.Inflammation, atherosclerosis, and coronary artery disease.N Engl J Med, 5,2(16): 1 685-695.
    [2] Simmons RD, Kumar S, Jo H.The role of endothelial mechanosensitive genes in atherosclerosis and omics approaches.Arch Biochem Biophys, 6,1(2): 111-131.
    [3] Tang F, Yang TL, Zhang Z, et al.MicroRNA-21 suppresses ox-LDL-induced human aortic endothelial cells injuries in atherosclerosis through enhancement of autophagic flux: involvement in promotion of lysosomal function.Exp Cell Res, 7,9(2): 374-383.
    [4] Eken SM, Jin H, Chernogubova E, et al.MicroRNA-210 enhances fibrous cap stability in advanced atherosclerotic lesions.Circ Res, 2017, 120(4): 633-644.
    [5] Cheng HS, Besla R, Li A, et al.Paradoxical suppression of atherosclerosis in the absence of microRNA-146a.Circ Res, 7,1(4): 354-367.
    [6] Chiu JJ, Chien S.Effects of disturbed flow on vascular endothelium: pathophysiological basis and clinical perspectives.Physiol Rev, 1,1(1): 327-387.
    [7] Bartel DP.MicroRNAs: target recognition and regulatory functions.Cell, 9,6(2): 215-233.
    [8] Neth P, Nazari-Jahantigh M, Schober A, et al.MicroRNAs in flow-dependent vascular remodelling.Cardiovasc Res, 3,9(2): 294-303.
    [9] Marin T, Gongol B, Chen Z, et al.Mechanosensitive microRNAs-role in endothelial responses to shear stress and redox state.Free Radic Biol Med, 3,4(6): 61-68.
    [10] Chen LJ, Chuang L, Huang YH, et al.MicroRNA mediation of endothelial inflammatory response to smooth muscle cells and its inhibition by atheroprotective shear stress.Circ Res, 5,6(7): 1 157-169.
    [11] Alexy T, James AM, Searles CD.Shear sensitive microRNAs and atherosclerosis.Biorheology, 4,1(2-3): 147-158.
    [12] Davies PF.Hemodynamic shear stress and the endothelium in cardiovascular pathophysiology.Nat Clin Pract Cardiovasc Med, 9,6(1): 16-26.
    [13] Kanthi Y, Hyman MC, Liao H, et al.Flow-dependent expression of ectonucleotide tri(di)phosphohydrolase-1 and suppression of atherosclerosis.J Clin Invest, 5,5(8): 3 027-036.
    [14] Qin X, Wang X, Wang Y, et al.MicroRNA-19a mediates the suppressive effect of laminar flow on cyclin D1 expression in human umbilical vein endothelial cells.Proc Natl Acad Sci USA, 0,7(7): 3 240-244.
    [15] 程彬彬.SIRT1与microRNA-34a在切应力诱导内皮祖细胞分化中的作用及其机制.上海交通大学, 2014: 50-51.
    [16] Weber M, Baker MB, Moore JP, et al.MiR-21 is induced in endothelial cells by shear stress and modulates apoptosis and eNOS activity.Biochem Biophys Res Commun, 0,3(4): 643-648.
    [17] Chao Y, Ye P, Zhu L, et al.Low shear stress induces endothelial reactive oxygen species via the AT1R/eNOS pathway.J Cell Physiol, 2017, 233(2): 1 384-395.
    [18] Alexy T, James AM, Searles CD.Shear sensitive microRNAs and atherosclerosis.Biorheology, 4,1(2-3): 147-158.
    [19] Ross R.Atherosclerosis--an inflammatory disease.N Engl J Med, 9,0(2): 115-126.
    [20] Nam D, Ni CW, Rezvan A, et al.Partial carotid ligation is a model of acutely induced disturbed flow, leading to rapid endothelial dysfunction and atherosclerosis.Am J Physiol Heart Circ Physiol, 9,7(4): H1 535-543.
    [21] Fan W, Fang R, Wu X, et al.Shear-sensitive microRNA-34a modulates flow-dependent regulation of endothelial inflammation.J Cell Sci, 5,8(1): 70-80.
    [22] Demolli S, Doebele C, Doddaballapur A, et al.MicroRNA-30 mediates anti-inflammatory effects of shear stress and KLF2 via repression of angiopoietin 2.J Mol Cell Cardiol, 5,8(11): 111-119.
    [23] Doran AC, Meller N, McNamara CA.Role of smooth muscle cells in the initiation and early progression of atherosclerosis.Arterioscler Thromb Vasc Biol, 8,8(5): 812-819.
    [24] Zhu JJ, Liu YF, Zhang YP, et al.VAMP3 and SNAP23 mediate the disturbed flow-induced endothelial microRNA secretion and smooth muscle hyperplasia.Proc Natl Acad Sci USA, 7,4(31): 8 271-276.
    [25] Zhou J, Li YS, Nguyen P, et al.Regulation of vascular smooth muscle cell turnover by endothelial cell-secreted microRNA-126:role of shear stress.Circ Res, 3,3(1): 40-51.
    [26] 马英英, 王璐, 包晗, 等.microRNA-133b在低切应力诱导血管内皮细胞影响血管平滑肌细胞增殖中的作用.医用生物力学, 6,1(5): 408-415.
    [27] 王聪聪, 姚庆苹, 马英英, 等.microRNA-34a在低切应力诱导血管平滑肌细胞增殖中的作用.医用生物力学, 5,0(4): 339-345.
    [28] Brown A J, Teng Z, Evans PC, et al.Role of biomechanical forces in the natural history of coronary atherosclerosis.Nat Rev Cardiol, 6,3(4): 210-220.
    [29] Chen PY, Qin L, Baeyens N, et al.Endothelial-to-mesenchymal transition drives atherosclerosis progression.J Clin Invest, 5,5(12): 4 514-528.
    [30] Wong WT, Ma S, Tian XY, et al.Targeted delivery of shear stress-inducible micrornas by nanoparticles to prevent vulnerable atherosclerotic lesions.Methodist Debakey Cardiovasc J, 6,2(3): 152-156.
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

LIU Jing, WANG Mei-Mei, HE Wen-Zhi, WEN Hong-Yan. The research progress of mechanism of microRNAs which regulated by shear stress on atherosclerosis[J]. Editorial Office of Chinese Journal of Arteriosclerosis,2017,25(12):1287-1290.

Copy
Share
Article Metrics
  • Abstract:1452
  • PDF: 699
  • HTML: 0
  • Cited by: 0
History
  • Received:March 12,2017
  • Revised:October 31,2017
  • Online: December 28,2017
Article QR Code