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Lectin-like Oxidized LDL Receptor 1 Is Involved in CRP-Mediated Complement Activation
Author(s) -
Yoshiko Fujita,
Saburo Yamaguchi,
Akemi Kakino,
Shin Iwamoto,
Ryo Yoshimoto,
Tatsuya Sawamura
Publication year - 2011
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/clinchem.2011.168625
Subject(s) - complement system , inflammation , lectin pathway , classical complement pathway , receptor , immunology , chemistry , c reactive protein , decay accelerating factor , antibody , medicine , biochemistry
C-reactive protein (CRP) is purported to be a risk factor that acts independently of LDL cholesterol in predicting all-cause mortality in patients with ischemic heart disease. Lectin-like oxidized LDL receptor 1 (LOX-1) impairs endothelial function and exacerbates myocardial injury. We recently demonstrated that CRP increased vascular permeability through direct binding to LOX-1. Here we examined, using a hypertensive rat model, whether LOX-1 is involved in CRP-induced complement activation.

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