Neutrophil antimicrobial peptide α-defensin causes endothelial dysfunction in porcine coronary arteries

Panagiotis Kougias, Hong Chai, Peter H. Lin, Qizhi Yao, Alan B. Lumsden, Changyi Chen

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

Background: Defensins are cysteine-rich cationic polypeptides released from neutrophils that exhibit powerful antimicrobial activities. Because inflammation, including neutrophil infiltration and release of defensins, may play an important role in atherosclerosis and other vascular diseases, we determined whether α-defensin could cause endothelial dysfunction, a major initial event of atherosclerosis, in porcine coronary arteries. Methods: Porcine coronary arteries were sliced into 5-mm rings and treated with different concentrations of human recombinant α-defensin for 24 hours. Vasomotor reactivity was studied by using a myograph system. Levels of superoxide anion were detected by the lucigenin-enhanced chemiluminescence method. Endothelial nitric oxide synthase (eNOS) messenger RNA (mRNA) and protein levels were determined by real-time polymerase chain reaction and immunohistochemistry analysis, respectively. Results: Endothelium-dependent relaxation in response to bradykinin was significantly reduced by 40% for the rings treated with 1500 nM of α-defensin compared with controls (P < .05). Vessel contractility in response to the thromboxane A2 analogue U46619 and endothelium-independent relaxation in response to sodium nitroprusside were not affected with defensin treatment. In addition, the superoxide anion level at the endothelial layer of porcine coronary artery rings was significantly increased by 80% in the defensin-treated (1500 nM) vessels compared with controls (P < .05). Furthermore, the eNOS mRNA levels in endothelial cells isolated from the cultured rings treated with defensin (1500 nM) were significantly decreased by 27% compared with controls (P < .05). Immunoreactivity of eNOS in the defensin-treated vessel rings was also substantially reduced. Conclusions: Defensin reduces the endothelium-dependent vasorelaxation. This effect is associated with increased superoxide radical production and decreased eNOS expression in porcine coronary arteries. Clinical Relevance: Inflammation is an important mechanism of atherosclerosis and other vascular diseases. The roles and interactions of biomediators released from inflammatory cells are not fully understood, however. This study provides new information about effects and potential molecular mechanisms of a major neutrophil releasing factor, α-defensin, on endothelial dysfunction of porcine coronary arteries. Thus, targeting α-defensin and its associated molecular mechanisms may become a new strategy to prevent vascular diseases.

Original languageEnglish (US)
Pages (from-to)357-363
Number of pages7
JournalJournal of Vascular Surgery
Volume43
Issue number2
DOIs
StatePublished - Feb 2006

ASJC Scopus subject areas

  • Surgery
  • Cardiology and Cardiovascular Medicine

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