Author
Listed:
- Hiroshi Suzuki
(Chugai Pharmaceutical Co. Ltd
Research Center for Advanced Science and Technology, University of Tokyo)
- Yukiko Kurihara
(University of Tokyo)
- Motohiro Takeya
(Kumamoto University School of Medicine)
- Nobuo Kamada
(Chugai Pharmaceutical Co. Ltd)
- Motoyukl Kataoka
(CSK Research Park Inc.)
- Kouichi Jishage
(Chugai Pharmaceutical Co. Ltd)
- Otoya Ueda
(Chugai Pharmaceutical Co. Ltd)
- Hisashl Sakaguchi
(Kumamoto University School of Medicine)
- Takayuki Higashi
(Kumamoto University School of Medicine)
- Tsukasa Suzuki
(Chugai Pharmaceutical Co. Ltd)
- Yoshiaki Takashima
(Chugai Pharmaceutical Co. Ltd)
- Yoshiki Kawabe
(Chugai Pharmaceutical Co. Ltd
Research Center for Advanced Science and Technology, University of Tokyo)
- Osamu Cynshi
(Chugai Pharmaceutical Co. Ltd)
- Youichiro Wada
(University of Tokyo)
- Makoto Honda
(University of Tokyo)
- Hiroki Kurihara
(University of Tokyo)
- Hiroyuki Aburatani
(University of Tokyo)
- Takefumi Doi
(Osaka University)
- Akiyo Matsumoto
(National Institute of Health and Nutrition)
- Sadahiro Azuma
(The University of Tokyo)
- Tetsuo Noda
(Cancer Institute)
- Yutaka Toyoda
(Obihiro University of Agriculture and Veterinary Medicine)
- Hiroshige Itakura
(National Institute of Health and Nutrition)
- Yoshio Yazaki
(University of Tokyo)
- Seikoh Horiuchi
(Kumamoto University School of Medicine)
- Kiyoshi Takahashi
(Kumamoto University School of Medicine)
- J. Kar Kruijt
(Leiden University)
- Theo J. C. van Berkel
(Leiden University)
- Urs P. Steinbrecher
(University of British Columbia)
- Shun Ishibashi
(University of Tokyo)
- Nobuyo Maeda
(School of Medicine, University of North Carolina)
- Siamon Gordon
(University of Oxford)
- Tatsuhiko Kodama
(Research Center for Advanced Science and Technology, University of Tokyo)
Abstract
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 pathogens7, and also mediates cation-independent macrophage adhesion in vitro8. 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.
Suggested Citation
Hiroshi Suzuki & Yukiko Kurihara & Motohiro Takeya & Nobuo Kamada & Motoyukl Kataoka & Kouichi Jishage & Otoya Ueda & Hisashl Sakaguchi & Takayuki Higashi & Tsukasa Suzuki & Yoshiaki Takashima & Yoshi, 1997.
"A role for macrophage scavenger receptors in atherosclerosis and susceptibility to infection,"
Nature, Nature, vol. 386(6622), pages 292-296, March.
Handle:
RePEc:nat:nature:v:386:y:1997:i:6622:d:10.1038_386292a0
DOI: 10.1038/386292a0
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