PHYSIOLOGICAL FLUID SHEAR-STRESS CAUSES DOWN-REGULATION OF ENDOTHELIN-1 MESSENGER-RNA IN BOVINE AORTIC ENDOTHELIUM

被引:242
作者
MALEK, A
IZUMO, S
机构
[1] BETH ISRAEL HOSP,MOLEC MED UNIT,INDURSKY LAB MOLEC CARDIOL,330 BROOKLINE AVE,BOSTON,MA 02215
[2] MIT,DIV HLTH SCI & TECHNOL,BOSTON,MA 02215
[3] HARVARD UNIV,SCH MED,BOSTON,MA 02115
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 263卷 / 02期
关键词
GENE REGULATION; MECHANICAL STRESS; DYNAMIC FORCES; VASOACTIVE SUBSTANCES; GROWTH SUBSTANCES; VESSEL STRUCTURE; ATHEROSCLEROSIS;
D O I
10.1152/ajpcell.1992.263.2.C389
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We report here that the level of endothelin-1 (ET-1) mRNA from bovine aortic endothelial cells grown in vitro is rapidly (within 1 h of exposure) and significantly (fivefold) decreased in response to fluid shear stress of physiological magnitude. The downregulation of ET-1 mRNA occurs in a dose-dependent manner that exhibits saturation above 15 dyn/cm2. The decrease is complete prior to detectable changes in endothelial cell shape and is maintained throughout and following alignment in the direction of blood flow. Peptide levels of ET-1 secreted into the media are also reduced in response to fluid shear stress. Cyclical stretch experiments demonstrated no changes in ET-1 mRNA, while increasing media viscosity with dextran showed that the downregulation is a specific response to shear stress and not to fluid velocity. Although both pulsatile and turbulent shear stress of equal time-average magnitude elicited the same decrease in ET-1 mRNA as steady laminar shear (15 dyn/cm2), low-frequency reversing shear stress did not result in any change. These results show that the magnitude as well as the dynamic character of fluid shear stress can modulate expression of ET-1 in vascular endothelium.
引用
收藏
页码:C389 / C396
页数:8
相关论文
共 31 条
  • [1] FLOW PATTERNS AND SPATIAL-DISTRIBUTION OF ATHEROSCLEROTIC LESIONS IN HUMAN CORONARY-ARTERIES
    ASAKURA, T
    KARINO, T
    [J]. CIRCULATION RESEARCH, 1990, 66 (04) : 1045 - 1066
  • [2] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [3] DAVIES PF, 1986, P NATL ACAD SCI USA, V83, P2114, DOI 10.1073/pnas.83.7.2114
  • [4] INFLUENCE OF HEMODYNAMIC FORCES ON VASCULAR ENDOTHELIAL FUNCTION - INVITRO STUDIES OF SHEAR-STRESS AND PINOCYTOSIS IN BOVINE AORTIC-CELLS
    DAVIES, PF
    DEWEY, CF
    BUSSOLARI, SR
    GORDON, EJ
    GIMBRONE, MA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (04) : 1121 - 1129
  • [5] FLUID-FLOW STIMULATES TISSUE PLASMINOGEN-ACTIVATOR SECRETION BY CULTURED HUMAN-ENDOTHELIAL CELLS
    DIAMOND, SL
    ESKIN, SG
    MCINTIRE, LV
    [J]. SCIENCE, 1989, 243 (4897) : 1483 - 1485
  • [6] FLOW EFFECTS ON PROSTACYCLIN PRODUCTION BY CULTURED HUMAN-ENDOTHELIAL CELLS
    FRANGOS, JA
    ESKIN, SG
    MCINTIRE, LV
    IVES, CL
    [J]. SCIENCE, 1985, 227 (4693) : 1477 - 1479
  • [7] INDUCTION OF HUMAN VASCULAR ENDOTHELIAL STRESS FIBERS BY FLUID SHEAR-STRESS
    FRANKE, RP
    GRAFE, M
    SCHNITTLER, H
    SEIFFGE, D
    MITTERMAYER, C
    DRENCKHAHN, D
    [J]. NATURE, 1984, 307 (5952) : 648 - 649
  • [8] ENDOTHELIUM-DERIVED RELAXING AND CONTRACTING FACTORS
    FURCHGOTT, RF
    VANHOUTTE, PM
    [J]. FASEB JOURNAL, 1989, 3 (09) : 2007 - 2018
  • [9] HUMAN VASCULAR ENDOTHELIAL CELLS IN CULTURE - GROWTH AND DNA-SYNTHESIS
    GIMBRONE, MA
    COTRAN, RS
    FOLKMAN, J
    [J]. JOURNAL OF CELL BIOLOGY, 1974, 60 (03) : 673 - 684
  • [10] GOLDSMITH HL, 1986, THROMB HAEMOSTASIS, V55, P415