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PMID: 7998959 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Binding characteristics of scavenger receptors on liver endothelial and Kupffer cells for modified low-density lipoproteins.

The Biochemical journal ·Vol. 304 ( Pt 1) ·1994-11-15 ·Pages 69-73

De Rijke YB, Biessen EA, Vogelezang CJ, van Berkel TJ

Abstract

Previous studies showed that both endothelial and Kupffer cells contain specific recognition sites of oxidized low-density lipoprotein (OxLDL), in addition to recognition sites which recognize OxLDL and acetylated LDL (AcLDL). We have determined the binding characteristics of the recognition sites for OxLDL on Kupffer cells and endothelial cells (OxLDL-specific binding-site) in comparison to the recognition site for AcLDL on endothelial cells, which recognizes both AcLDL and OxLDL (Ac/OxLDL binding site). The capacity of Kupffer cells to bind OxLDL (Bmax. = 779 ng of 125I-OxLDL/mg of cell protein; Kd = 6 micrograms/ml) was comparable to the binding-capacity of endothelial cells (Bmax. = 803 ng of 125I-OxLDL/mg of cell protein; Kd = 5 micrograms/ml). The effect of net charge of modified LDL on its affinity for the recognition sites on Kupffer and endothelial cells was evaluated using competition studies. The affinity of AcLDL for the Ac/OxLDL binding site was greatly increased from 460 micrograms/ml to 4 micrograms/ml with increasing extent of modification and thus net charge. The Ac/OxLDL binding-site on endothelial cells also displayed an increased affinity towards LDL with an increasing degree of oxidation. The affinity of OxLDL for the Ac/OxLDL binding-site appeared to be about 4-fold higher than that of AcLDL with a similar extent of modification. At higher degrees of oxidation of LDL, the affinity for the OxLDL-specific site on endothelial and Kupffer cells was also strongly enhanced; the OxLDL-specific binding-site possesses a higher affinity for mildly oxidized LDL as compared with the Ac/OxLDL binding-site. It is concluded that recognition of OxLDL by both the OxLDL-specific binding-site and the Ac/OxLDL binding-site on liver endothelial and Kupffer cells depends on the net negative charge of modified LDL. The similarity in binding pattern of these binding sites makes it likely that the newly described 95 kD OxLDL binding protein on Kupffer cells [Y. B. De Rijke and Th. J. C. van Berkel, J. Biol. Chem. (1994), 269, 824-827] contains a recognition site with similar structural elements as described earlier for scavenger receptors.

MeSH Terms
Binding Sites Endothelium/metabolism Humans Kupffer Cells/metabolism Lipoproteins, LDL/metabolism Liver/metabolism Membrane Proteins Radioligand Assay Receptors, Immunologic/metabolism Receptors, Lipoprotein Receptors, Scavenger Scavenger Receptors, Class B
Chemicals
Lipoproteins, LDL Membrane Proteins Receptors, Immunologic Receptors, Lipoprotein Receptors, Scavenger Scarb1 protein, mouse Scavenger Receptors, Class B
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
De Rijke Y B
Division of Biopharmaceutics, Leiden-Amsterdam Center for Drug Research (LACDR), Sylvius Laboratories, University of Leiden, The Netherlands.
Biessen E A
Vogelezang C J
van Berkel T J
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1994-11-15
Pages
69-73
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1137453
Subset
IM
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