Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction

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Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction. / Abdo, Adrian; Rayner, B.S.; van Reyk, D.M.; Hawkins, C.L.

In: Redox Biology, Vol. 13, 2017, p. 623-632.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Abdo, A, Rayner, BS, van Reyk, DM & Hawkins, CL 2017, 'Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction', Redox Biology, vol. 13, pp. 623-632. https://doi.org/10.1016/j.redox.2017.08.004

APA

Abdo, A., Rayner, B. S., van Reyk, D. M., & Hawkins, C. L. (2017). Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction. Redox Biology, 13, 623-632. https://doi.org/10.1016/j.redox.2017.08.004

Vancouver

Abdo A, Rayner BS, van Reyk DM, Hawkins CL. Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction. Redox Biology. 2017;13:623-632. https://doi.org/10.1016/j.redox.2017.08.004

Author

Abdo, Adrian ; Rayner, B.S. ; van Reyk, D.M. ; Hawkins, C.L. / Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction. In: Redox Biology. 2017 ; Vol. 13. pp. 623-632.

Bibtex

@article{6b7ca81b25084726b9e3ba684e6eeaad,
title = "Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction",
abstract = "Low-density lipoprotein (LDL) modified by hypochlorous acid (HOCl) produced by myeloperoxidase (MPO) is present in atherosclerotic lesions, where it is implicated in the propagation of inflammation and acceleration of lesion development by multiple pathways, including the induction of endothelial dysfunction. Thiocyanate (SCN-) ions are utilised by MPO to produce the oxidant hypothiocyanous acid (HOSCN), which reacts with LDL in a different manner to HOCl. Whilst the reactivity of HOCl-modified LDL has been previously studied, the role of HOSCN in the modification of LDL in vivo is poorly defined, although emerging evidence suggests that these particles have distinct biological properties. This is important because elevated plasma SCN- is linked with both the propagation and prevention of atherosclerosis. In this study, we demonstrate that both HOSCN- and HOCl-modified LDL inhibit endothelium-mediated vasorelaxation ex vivo in rat aortic ring segments. In vitro experiments with human coronary artery endothelial cells show that HOSCN-modified LDL decreases in the production of nitric oxide (NO•) and induces the loss of endothelial nitric oxide synthase (eNOS) activity. This occurs to a similar extent to that seen with HOCl-modified LDL. In each case, these effects are related to eNOS uncoupling, rather than altered expression, phosphorylation or cellular localisation. Together, these data provide new insights into role of MPO and LDL modification in the induction of endothelial dysfunction, which has implications for both the therapeutic use of SCN- within the setting of atherosclerosis and for smokers, who have elevated plasma levels of SCN-, and are more at risk of developing cardiovascular disease.",
author = "Adrian Abdo and B.S. Rayner and {van Reyk}, D.M. and C.L. Hawkins",
year = "2017",
doi = "10.1016/j.redox.2017.08.004",
language = "English",
volume = "13",
pages = "623--632",
journal = "Redox Biology",
issn = "2213-2317",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Low-density lipoprotein modified by myeloperoxidase oxidants induces endothelial dysfunction

AU - Abdo, Adrian

AU - Rayner, B.S.

AU - van Reyk, D.M.

AU - Hawkins, C.L.

PY - 2017

Y1 - 2017

N2 - Low-density lipoprotein (LDL) modified by hypochlorous acid (HOCl) produced by myeloperoxidase (MPO) is present in atherosclerotic lesions, where it is implicated in the propagation of inflammation and acceleration of lesion development by multiple pathways, including the induction of endothelial dysfunction. Thiocyanate (SCN-) ions are utilised by MPO to produce the oxidant hypothiocyanous acid (HOSCN), which reacts with LDL in a different manner to HOCl. Whilst the reactivity of HOCl-modified LDL has been previously studied, the role of HOSCN in the modification of LDL in vivo is poorly defined, although emerging evidence suggests that these particles have distinct biological properties. This is important because elevated plasma SCN- is linked with both the propagation and prevention of atherosclerosis. In this study, we demonstrate that both HOSCN- and HOCl-modified LDL inhibit endothelium-mediated vasorelaxation ex vivo in rat aortic ring segments. In vitro experiments with human coronary artery endothelial cells show that HOSCN-modified LDL decreases in the production of nitric oxide (NO•) and induces the loss of endothelial nitric oxide synthase (eNOS) activity. This occurs to a similar extent to that seen with HOCl-modified LDL. In each case, these effects are related to eNOS uncoupling, rather than altered expression, phosphorylation or cellular localisation. Together, these data provide new insights into role of MPO and LDL modification in the induction of endothelial dysfunction, which has implications for both the therapeutic use of SCN- within the setting of atherosclerosis and for smokers, who have elevated plasma levels of SCN-, and are more at risk of developing cardiovascular disease.

AB - Low-density lipoprotein (LDL) modified by hypochlorous acid (HOCl) produced by myeloperoxidase (MPO) is present in atherosclerotic lesions, where it is implicated in the propagation of inflammation and acceleration of lesion development by multiple pathways, including the induction of endothelial dysfunction. Thiocyanate (SCN-) ions are utilised by MPO to produce the oxidant hypothiocyanous acid (HOSCN), which reacts with LDL in a different manner to HOCl. Whilst the reactivity of HOCl-modified LDL has been previously studied, the role of HOSCN in the modification of LDL in vivo is poorly defined, although emerging evidence suggests that these particles have distinct biological properties. This is important because elevated plasma SCN- is linked with both the propagation and prevention of atherosclerosis. In this study, we demonstrate that both HOSCN- and HOCl-modified LDL inhibit endothelium-mediated vasorelaxation ex vivo in rat aortic ring segments. In vitro experiments with human coronary artery endothelial cells show that HOSCN-modified LDL decreases in the production of nitric oxide (NO•) and induces the loss of endothelial nitric oxide synthase (eNOS) activity. This occurs to a similar extent to that seen with HOCl-modified LDL. In each case, these effects are related to eNOS uncoupling, rather than altered expression, phosphorylation or cellular localisation. Together, these data provide new insights into role of MPO and LDL modification in the induction of endothelial dysfunction, which has implications for both the therapeutic use of SCN- within the setting of atherosclerosis and for smokers, who have elevated plasma levels of SCN-, and are more at risk of developing cardiovascular disease.

U2 - 10.1016/j.redox.2017.08.004

DO - 10.1016/j.redox.2017.08.004

M3 - Journal article

VL - 13

SP - 623

EP - 632

JO - Redox Biology

JF - Redox Biology

SN - 2213-2317

ER -

ID: 194803723