Human macrophage scavenger receptors: Primary structure, expression, and localization in atherosclerotic lesions
- Univ. of Tokyo (Japan) National Inst. of Health and Nutrition, Tokyo (Japan)
- Kumamoto Univ. (Japan)
- National Inst. of Health and Nutrition, Tokyo (Japan)
- Univ. of Tokyo (Japan)
- Univ. of Tokyo (Japan) Massachusetts Inst. of Tech., Cambridge, MA (United States)
- Chugai Pharmaceutical, Tokyo (Japan)
- Genzyme Corp., Framingham, MA (United States)
- Massachusetts Inst. of Tech., Cambridge (United States)
Two types of cDNAs for human macrophage scavenger receptors were cloned from a cDNA library derived from the phorbol ester-treated human monocytic cell line THP-1. The type I and type II human scavenger receptors encoded by these cDNAs are homologous (73% and 71% amino acid identity) to their previously characterized bovine counterparts and consist of six domains: cytoplasmic (I), membrane-spanning (II), spacer (III), {alpha}-helical coiled-coil (IV), collagen-like (V), and a type-specific C-terminal (VI). The receptor gene is located on human chromosome 8. The human receptors expressed in CHO-K1 cells mediated endocytosis of modified low density lipoproteins. Two mRNAs, 4.0 and 3.2 kilobases, have been detected in human liver, placenta, and brain. Immunohistochemical studies using an anti-peptide antibody which recognizes human scavenger receptors indicated the presence of the scavenger receptors in the macrophages of lipid-rich atherosclerotic lesions, suggesting the involvement of scavenger receptors in atherogenesis.
- OSTI ID:
- 6144540
- Journal Information:
- Proceedings of the National Academy of Sciences of the United States of America; (United States), Vol. 87:23; ISSN 0027-8424
- Country of Publication:
- United States
- Language:
- English
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550201* - Biochemistry- Tracer Techniques