The murine macrophage apoB-48 receptor gene (Apob-48r):: homology to the human receptor

被引:13
作者
Brown, ML
Yui, K
Smith, JD
LeBoeuf, RC
Weng, W
Umeda, PK
Li, R
Song, RL
Gianturco, SH [1 ]
Bradley, WA
机构
[1] Univ Alabama, Dept Med, Div Gerontol & Geriatr, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Med, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[3] Tokyo Med & Dent Univ, Dept Internal Med 3, Bunkyo Ku, Tokyo 1138519, Japan
[4] Rockefeller Univ, New York, NY 10021 USA
[5] Univ Washington, Dept Pathobiol, Seattle, WA 98195 USA
[6] InGenious Targeting Lab, Stony Brook, NY 11790 USA
关键词
atherosclerosis; chylomicrons; hypertriglyceridemia; postprandial lipoproteins;
D O I
10.1194/jlr.M100395-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Previously we cloned the human macrophage apolipoprotein B-48 receptor (ApoB48R) and documented its expression in human atherosclerotic foam cells (1). Now we have identified and characterized the murine macrophage apob-48r cDNA gene sequence and its chromasomal location. The cDNA (3,615 bp) -deduced amino acid (aa) sequence (942 aa) is similar to45% identical to the human macrophage APOB-48R, but not to other known gene families. The murine Apob-48r gene, like the human APOB-48R gene, consists of four exons interrupted by three small introns and is syntenically located on chromosome 7. Functionally significant conserved domains include an N-terminal hydrophobic domain, a glycosaminoglycan attachment site, an N-glycosylation site, and an ExxxLL internalization motif C-terminal to the putative internal transmembrane domain. Two conserved coiled-coil domains are likely involved in the spontaneous homodimerization that generates the active dimeric ligand binding species (mouse, similar to190 kDa; human, similar to200 kDa). Transfection of the murine apoB-48R into Chinese hamster ovary cells (CHOs) confers apoB-48R function: rapid, high-affinity, specific uptake of known triglyceride-rich lipoprotein ligands of the apoB-48R and, of note, uptake of the cholesteryl ester-rich apoB-48-containing very low density lipoproteins that accumulate in atherosclerosis-prone apoE-deficient mice. Uptake of these ligands by murine apoB-48R-transfected CHOs causes saturable, visible cellular triglyceride and cholesterol accumulation in vitro that resemble foam cells of atherosclerotic lesions. In aggregate, the data presented here and that previously published suggest that the apoE-independent murine apo-B48R pathway may contribute to the spontaneous development of atherosclerotic lesions rich in macrophage-derived foam cells observed in apoE-deficient mice, a murine model of human atherosclerosis.-Brown, M. L., K. Yui, J. D. Smith, R. C. LcBoeuf, W. Weng, P. K. Umeda, R. Li, R. Song, S. H. Gianturco, and W. A. Bradley. The murine macrophage apoB-48 receptor gene (ApoB-48r): homology to the human receptor. J. Lipid. Res. 2002. 43: 1181-1191.
引用
收藏
页码:1181 / 1191
页数:11
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