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   <subfield code="a">Oxidative modifications of low-density lipoproteins (LDL) by the human endothelial cell line EA.hy 926</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. Pech-Amsellem, I. Myara, I. Pico, C. Mazière, J. Mazière, N. Moatti]</subfield>
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   <subfield code="a">Modifications of LDL by the EA.hy 926 cell line were compared to those generated by human umbilical vein endothelial cells (HUVEC). Thiobarbituric acid reactive substances (TBARS) index values (TBARS sample/TBARS cell-free control ratio) were 2.64±0.18 (m±SE, n=11) and 3.12±0.24 (n=11), for HUVEC and EA.hy 926, respectively. The percentage of the most electronegative modified LDL fraction (fraction C), assessed by using an ion-exchange chromatographic method based on fast protein liquid chromatography (FPLC), represented 14±3% (n=34) and 22±13% (n=10) of total modified LDL in HUVEC and EA.hy 926, respectively. LDL modified by both cell lines showed increased agarose electrophoretic mobility and apo B100 fragmentation on SDS-PAGE. None of the results were significantly different between the two cell lines. Superoxide anion production was 0.12±0.04 (n=11) and 0.07±0.01 nmol/min/mg cell protein (n=11) in HUVEC and EA.hy 926, respectively. Cell-specific effects on LDL were abrogated in cysteine-free medium. Moreover, cell-modified LDL were similarly degraded by J774 macrophage-like cells. We conclude that EA.hy 926 cells are a good model for investigating endothelial cell-induced modifications of LDL. Advantages include ready availability and less individual variability than with HUVEC.</subfield>
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   <subfield code="a">LDL peroxidation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">low-density lipoprotein</subfield>
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   <subfield code="a">endothelial cell</subfield>
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   <subfield code="a">thiol</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">atherosclerosis</subfield>
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   <subfield code="a">FPLC</subfield>
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   <subfield code="a">LDL : low-density lipoprotein</subfield>
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   <subfield code="a">HAT : 100 μM hypoxanthine/0.4 μM aminopterin/16 μM thymidine</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">FCS : fetal calf serum</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">TBARS : thiobarbituric acid-reactive substances (lipid peroxidation products)</subfield>
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   <subfield code="a">MDA : malondialdehyde</subfield>
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   <subfield code="a">FPLC : fast protein liquid chromatography</subfield>
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   <subfield code="a">cpm : counts per minute</subfield>
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   <subfield code="a">Pech-Amsellem</subfield>
   <subfield code="D">M.</subfield>
   <subfield code="u">Faculté de Pharmacie, Laboratoire de Biochimie Appliquée, F-92296, Châtenay-Malabry</subfield>
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   <subfield code="D">I.</subfield>
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   <subfield code="a">Mazière</subfield>
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   <subfield code="a">Mazière</subfield>
   <subfield code="D">J.</subfield>
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   <subfield code="a">Moatti</subfield>
   <subfield code="D">N.</subfield>
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   <subfield code="t">Experientia</subfield>
   <subfield code="d">Birkhäuser-Verlag</subfield>
   <subfield code="g">52/3(1996-03-01), 234-238</subfield>
   <subfield code="x">0014-4754</subfield>
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