Angiotensin II induces LOX-1, the human endothelial receptor for oxidized low-density lipoprotein

Oxidatively modified LDL (oxLDL) plays an important role in the development of atherosclerosis. OxLDL effects, eg, foam cell formation, are mediated in part by the classic scavenger receptor, whereas other effects may involve the recently cloned endothelial oxLDL receptor, LOX-1 (lectinlike oxLDL re...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 1999-08, Vol.100 (9), p.899-902
Hauptverfasser: MORAWIETZ, H, RUECKSCHLOSS, U, NIEMANN, B, DUERRSCHMIDT, N, GALLE, J, HAKIM, K, ZERKOWSKI, H.-R, SAWAMURA, T, HOLTZ, J
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Sprache:eng
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Zusammenfassung:Oxidatively modified LDL (oxLDL) plays an important role in the development of atherosclerosis. OxLDL effects, eg, foam cell formation, are mediated in part by the classic scavenger receptor, whereas other effects may involve the recently cloned endothelial oxLDL receptor, LOX-1 (lectinlike oxLDL receptor-1), which is distinct from macrophage scavenger receptors. Because the regulation of LOX-1 must still be defined, we investigated whether LOX-1 is regulated by the potentially proatherosclerotic stimulant angiotensin II (Ang II). Using competitive reverse transcription-polymerase chain reaction (RT-PCR), we quantified mRNA expression of LOX-1 in primary cultures of human umbilical vein endothelial cells (HUVECs). After treatment with Ang II for 3 hours (1 nmol/L to 1 micromol/L), LOX-1 mRNA was concentration-dependently induced (from 6.9+/-1.4 to 23.1+/-5.5 relative units [RU] by 1 micromol/L Ang II; P
ISSN:0009-7322
1524-4539
DOI:10.1161/01.cir.100.9.899