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S-homocysteinylated LDL apolipoprotein B adversely affects human endothelial cells in vitro

Zinellu, Angelo and Sotgia, Salvatore and Scanu, Bastianina and Pintus, Gianfranco and Posadino, Anna Maria and Cossu, Annalisa and Deiana, Luca and Sengupta, Shantanu and Carru, Ciriaco (2009) S-homocysteinylated LDL apolipoprotein B adversely affects human endothelial cells in vitro. Atherosclerosis, Vol. 206 (1), p. 40-46. ISSN 0021-9150. Article.

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DOI: 10.1016/j.atherosclerosis.2009.01.035

Abstract

Objective. In recent years elevated homocysteine (Hcy) levels have been widely recognized as a risk factor for cardiovascular diseases (CVDs) and a connection between hyperhomocysteinemia and lipid metabolism has been suggested to have a possible role in endothelial vascular damage as lipoprotein fractions contain higher Hcy levels in hypercholesterolemia, compared to normolipidemic individuals. However, the biochemical events underlying the interaction between Hcy and LDL are still poorly understood.
Methods and results. Herein we have investigated the interaction of LDL with Hcy by measuring thiols S-linked to apoprotein using capillary electrophoresis and have evaluated the effect of S-homocysteinylated LDL on human endothelial cells (HECs). We found that Hcy binds to LDL in a dose dependent manner and the saturation binding is achieved at 100 μmol/L Hcy in about 5 h. Addition of Hcy resulted in a rapid displacement of other thiols bound to apoprotein and this was dependent on the concentration of Hcy added. For the first time we also demonstrated that treatment of HECs with homocysteine-S-LDL (Hcy-S-LDL) resulted in the induction of significantly higher levels of reactive oxygen species (ROS) compared to N-LDL (native LDL). Furthermore, the Hcy-S-LDL-induced a rise in intracellular ROS production was followed by a marked reduction of HECs proliferation and viability.
Conclusions. Although the mechanism by which Hcy-S-LDL elicits the current cellular effects needs further investigation, our data suggest that intracellular ROS production induced by Hcy-S-LDL might be responsible for the observed HECs damage and indicate that Hcy-S-LDL may have some role in CVD.

Item Type:Article
ID Code:3501
Status:Published
Refereed:Yes
Uncontrolled Keywords:S-homocysteinylation, LDL, homocysteine, human endothelial cells, reactive oxygen species (ROS)
Subjects:Area 05 - Scienze biologiche > BIO/10 Biochimica
Area 05 - Scienze biologiche > BIO/12 Biochimica clinica e biologia molecolare clinica
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze biomediche
Publisher:Elsevier Ireland
ISSN:0021-9150
Deposited On:22 Jan 2010 12:50

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