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Induction of the OxLDL receptor LOX-1 by endothelin-1 in human endothelial cells
被引:92
|作者:
Morawietz, H
Duerrschmidt, N
Niemann, B
Galle, J
Sawamura, T
Holtz, J
机构:
[1] Univ Halle Wittenberg, Fac Med, Inst Pathophysiol, D-06097 Halle, Germany
[2] Univ Wurzburg, Clin Internal Med, Wurzburg, Germany
[3] Natl Cardiovasc Ctr, Res Inst, Dept Biosci, Osaka, Japan
关键词:
atherosclerosis;
endothelial cells;
endothelin-1;
low-density lipoprotein;
D O I:
10.1006/bbrc.2001.5044
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In this study, we analyzed the effect of endothelin-l (ET-1) on expression of the lectin-like oxidized low-density lipoprotein (oxLDL) receptor-1 LOX-1 and on oxLDL uptake in primary cultures of human umbilical vein endothelial cells (HUVEC). LOX-1 mRNA was quantified by standard-calibrated competitive RT-PCR, LOX-1 protein expression by Western analysis and endothelial oxLDL uptake using DiI-labeled oxLDL, ET-1 induces LOX-1 mRNA expression, reaching its maximum after 1 h (160 +/- 14% of control, 100 nM ET-1, P < 0.05). This increased ET-1-mediated LOX-1 mRNA expression could be inhibited by endothelin receptor B antagonist BQ-788. In addition, ET-1 stimulates LOX-1 protein expression and oxLDL uptake in HUVEC, The augmented oxLDL uptake by ET-1 is mediated by endothelin receptor B, but not by protein kinases. These data support a new pathophysiological mechanism how locally and systemically increased ET-1 levels could promote LOX-l-mediated oxLDL uptake in human endothelial cells and the development and progression of endothelial dysfunction and atherosclerosis. (C) 2001 Academic Press.
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页码:961 / 965
页数:5
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