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Cited by 443

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Deletion of LOX-1 Reduces Atherogenesis in LDLR Knockout Mice Fed High Cholesterol Diet

Open access
Mehta, Jawahar L., Sanada, Nobuhito, Hu, Chang Ping, Chen, Jiawei, Dandapat, Abhijit, Sugawara, Fumiaki, Satoh, Hiroo, Inoue, Kazuhiko, Kawase, Yosuke, Jishage, Kou-ichi, Suzuki, Hiroshi, Takeya, Motohiro, Schnackenberg, Laura, Beger, Richard, Hermonat, Paul L., Thomas, Maria, Sawamura, Tatsuya·2007·Circulation Research

Abstract

Atherosclerosis is associated with oxidative stress and inflammation, and upregulation of LOX-1, an endothelial receptor for oxidized LDL (oxLDL). Here, we describe generation of LOX-1 knockout (KO) mice in which binding of oxLDL to aortic endothelium was reduced and endothelium-dependent vasorelaxation preserved after treatment with oxLDL ( P <0.01 versus wild-type mice). To address whether endothelial functional preservation might lead to reduction in atherogenesis, we crossed LOX-1 KO mice with LDLR KO mice and fed these mice 4% cholesterol/10% cocoa butter diet for 18 weeks. Atherosclerosis was found to cover 61±2% of aorta in the LDLR KO mice, but only 36±3% of aorta in the double KO mice. Luminal obstruction and intima thickness were significantly reduced in the double KO mice (versus LDLR KO mice). Expression of redox-sensitive NF-κB and the inflammatory marker CD68 in LDLR KO mice was increased ( P <0.01 versus wild-type mice), but not in the double KO mice. On the other hand, antiinflammatory cytokine IL-10 expression and superoxide dismutase activity were low in the LDLR KO mice ( P <0.01 versus wild-type mice), but not in the double KO mice. Endothelial nitric oxide synthase expression was also preserved in the double KO mice. The proinflammatory signal MAPK P38 was activated in the LDLR KO mice, and LOX-1 deletion reduced this signal. In conclusion, LOX-1 deletion sustains endothelial function leading to a reduction in atherogenesis in association with reduction in proinflammatory and prooxidant signals.

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Crossref · 10.1161/circresaha.107.149724

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Metadata

Authors
Mehta, J. L., Sanada, N., Hu, C. P., Chen, J., Dandapat, A., Sugawara, F., Satoh, H., Inoue, K., Kawase, Y., Jishage, K.-I., Suzuki, H., Takeya, M., Schnackenberg, L., Beger, R., Hermonat, P. L., Thomas, M., & Sawamura, T.
Venue
Circulation Research
Published
2007-06-08
Volume
100
Issue
11
Pages
1634-1642
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W2159036039
Cited by
443
References
1
FWCI
8.88
Type
journal article
Language
en
Open access
bronze

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