A role for macrophage scavenger receptors in atherosclerosis and susceptibility to infection

Macrophage type-I and type-II class-A scavenger receptors (MSR-A) are implicated in the pathological deposition of cholesterol during atherogenesis as a result of receptor-mediated uptake of modified low-density lipoproteins (mLDL) 1–6 . MSR-A can bind an extraordinarily wide range of ligands, inclu...

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Veröffentlicht in:Nature (London) 1997-03, Vol.386 (6622), p.292-296
Hauptverfasser: Suzuki, Hiroshi, Kurihara, Yukiko, Takeya, Motohiro, Kamada, Nobuo, Kataoka, Motoyukl, Jishage, Kouichi, Ueda, Otoya, Sakaguchi, Hisashl, Higashi, Takayuki, Suzuki, Tsukasa, Takashima, Yoshiaki, Kawabe, Yoshiki, Cynshi, Osamu, Wada, Youichiro, Honda, Makoto, Kurihara, Hiroki, Aburatani, Hiroyuki, Doi, Takefumi, Matsumoto, Akiyo, Azuma, Sadahiro, Noda, Tetsuo, Toyoda, Yutaka, Itakura, Hiroshige, Yazaki, Yoshio, Horiuchi, Seikoh, Takahashi, Kiyoshi, Kruijt, J. Kar, van Berkel, Theo J. C, Steinbrecher, Urs P, Ishibashi, Shun, Maeda, Nobuyo, Gordon, Siamon, Kodama, Tatsuhiko
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Sprache:eng
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Zusammenfassung:Macrophage type-I and type-II class-A scavenger receptors (MSR-A) are implicated in the pathological deposition of cholesterol during atherogenesis as a result of receptor-mediated uptake of modified low-density lipoproteins (mLDL) 1–6 . MSR-A can bind an extraordinarily wide range of ligands, including bacterial pathogens 7 , and also mediates cation-independent macrophage adhesion in vitro 8 . Here we show that targeted disruption of the MSR-A gene in mice results in a reduction in the size of atherosclerotic lesions in an animal deficient in apolipoprotein E. Macrophages from MSR-A-deficient mice show a marked decrease in mLDL uptake in vitro , whereas mLDL clearance from plasma occurs at a normal rate, indicating that there may be alternative mechanisms for removing mLDL from the circulation. In addition, MSR-A-knockout mice show an increased susceptibility to infection with Listeria monocytogenes or herpes simplex virus type-1, indicating that MSR-A may play a part in host defence against pathogens.
ISSN:0028-0836
1476-4687
DOI:10.1038/386292a0