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Title: Human macrophage scavenger receptors: Primary structure, expression, and localization in atherosclerotic lesions

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America; (United States)
; ;  [1]; ;  [2]; ; ;  [3]; ;  [4];  [5]; ; ;  [6]; ;  [7];  [8]
  1. Univ. of Tokyo (Japan) National Inst. of Health and Nutrition, Tokyo (Japan)
  2. Kumamoto Univ. (Japan)
  3. National Inst. of Health and Nutrition, Tokyo (Japan)
  4. Univ. of Tokyo (Japan)
  5. Univ. of Tokyo (Japan) Massachusetts Inst. of Tech., Cambridge, MA (United States)
  6. Chugai Pharmaceutical, Tokyo (Japan)
  7. Genzyme Corp., Framingham, MA (United States)
  8. 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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