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2011 | 58 | 3 | 375-379
Article title

Influence of elastin-derived peptides, glucose, LDL and oxLDL on nitric oxide synthase expression in human umbilical artery endothelial cells

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EN
Abstracts
EN
Endothelial dysfunction plays an important role in the development of atherosclerosis. Elastin-derived peptides (EDP), hyperglycemia, hypercholesterolemia and oxidized LDL have a proven proatherosclerotic potential. Nitric oxide generated by endothelial nitric oxide synthase (eNOS; EC 1.14.13.39) is an important vasorelaxant. Here we studied the influence of those proatherosclerotic factors on eNOS gene and protein expression in artery-derived endothelial cells. Human umbilical artery endothelial cells (HUAEC) were incubated with or without: glucose (270 mg/dl), LDL (200 mg/dl), oxidized LDL (oxLDL 25 mg/dl) or κ-elastin (0.5 and 2.5 µg/ml). Gene expression was assessed by real time RT-PCR, whilst the eNOS protein by ELISA. In cells incubated with 2.5 µg/ml of κ-elastin, a 31 % increase of eNOS mRNA expression was observed, but the protein level remained unchanged. OxLDL, LDL and glucose decreased the eNOS protein level by 74 %, 37 % and 29 %, respectively. OxLDL decreased eNOS mRNA by 42 %. LDL non-significantly decreased eNOS mRNA expression. An elevated glucose level did not affect the eNOS mRNA expression. Hyperglycemia and an elevated level of LDL, particularly oxLDL, decreased the level of eNOS protein in endothelial cells. As κ-elastin did not decrease the expression of eNOS gene in HUAEC, the proatherogenic properties of elastin-derived peptides are unlikely to be due to their influence on eNOS.
Publisher

Year
Volume
58
Issue
3
Pages
375-379
Physical description
Dates
published
2011
received
2011-03-05
revised
2011-03-27
accepted
2011-07-09
(unknown)
2011-07-11
Contributors
  • Department of Biochemistry, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, Medical University of Silesia, Katowice, Poland
author
  • Department of Biochemistry, Medical University of Silesia, Katowice, Poland
  • Department of Human Anatomy, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, Medical University of Silesia, Katowice, Poland
  • Department of Molecular Biology, Medical University of Silesia, Sosnowiec, Poland
References
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Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.bwnjournal-article-abpv58p375kz
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