• Title of article

    Hemodynamics influences vascular peroxynitrite formation: Implication for low-density lipoprotein apo-B-100 nitration

  • Author/Authors

    Tzung K. Hsiai، نويسنده , , Juliana Hwang، نويسنده , , Mark L. Barr، نويسنده , , Adria Correa، نويسنده , , Ryan Hamilton، نويسنده , , Mohammad Alavi، نويسنده , , Mahsa Rouhanizadeh، نويسنده , , Enrique Cadenas، نويسنده , , Stanley L. Hazen، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2007
  • Pages
    11
  • From page
    519
  • To page
    529
  • Abstract
    Hemodynamics, specifically, fluid shear stress, modulates the focal nature of atherogenesis. Superoxide anion (O2− ) reacts with nitric oxide ( NO) at a rapid diffusion-limited rate to form peroxynitrite (O2− + NO → ONOO−). Immunohistostaining of human coronary arterial bifurcations or curvatures, where OSS develops, revealed the presence of nitrotyrosine staining, a fingerprint of peroxynitrite; whereas in straight segments, where PSS occurs, nitrotyrosine was absent. We examined vascular nitrative stress in models of oscillatory (OSS) and pulsatile shear stress (PSS). Bovine aortic endothelial cells (BAEC) were exposed to fluid shear stress that simulates arterial blood flow: (1) PSS at a mean shear stress (τave) of 23 dyn cm− 2 and a temporal gradient (∂τ/∂t) at 71 dyn cm− 2 s− 1, and (2) OSS at τave = 0.02 dyn cm− 2 and ∂τ/∂t = ± 3.0 dyn cm− 2 s− 1 at a frequency of 1 Hz. OSS significantly up-regulated one of the NADPH oxidase subunits (NOx4) expression accompanied with an increase in O2− production. In contrast, PSS up-regulated eNOS expression accompanied with NO production (total NO2− and NO3−). To demonstrate that O2− and NO are implicated in ONOO− formation, we added low-density lipoprotein cholesterol (LDL) to the medium in which BAEC were exposed to the above flow conditions. The medium was analyzed for LDL apo-B-100 nitrotyrosine by liquid chromatography electrospray ionization tandem mass spectrometry (LC/ESI/MS/MS). OSS induced higher levels of 3-nitrotyrosine, dityrosine, and o-hydroxyphenylalanine compared with PSS. In the presence of ONOO−, specific apo-B-100 tyrosine residues underwent nitration in the α and β helices: α-1 (Tyr144), α-2 (Tyr2524), β-2 (Tyr3295), α-3 (Tyr4116), and β-2 (Tyr4211). Hence, the characteristics of shear stress in the arterial bifurcations influenced the relative production of O2− and NO with an implication for ONOO− formation as evidenced by LDL protein nitration.
  • Keywords
    superoxide anion , nitrotyrosine , LDL , Shear stress , nitric oxide
  • Journal title
    Free Radical Biology and Medicine
  • Serial Year
    2007
  • Journal title
    Free Radical Biology and Medicine
  • Record number

    520849