Home LiteratureArticle Details
PMID: 3655562 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Turnover and tissue sites of degradation of glucosylated low density lipoprotein in normal and immunized rabbits.

Journal of lipid research ·Vol. 28 ·No. 9 ·1987-09-00 ·Pages 1098-109

Wiklund O, Witztum JL, Carew TE, Pittman RC, Elam RL, Steinberg D

Abstract

Immunological mechanisms have been implicated in the atherogenic process since immunoglobulins are frequently found in the atherosclerotic aorta. We have previously shown that modifications of homologous low density lipoproteins (LDL) make it immunogenic. In particular we have demonstrated that immunization with homologous nonenzymatically glucosylated LDL (glcLDL) results in the generation of antibodies specific to the derivatized lysine residue, and that such antibodies do not react with native LDL epitopes. In the present study we immunized rabbits with reductively glucosylated rabbit LDL and then determined the effects of the circulating antibodies on the rates of plasma clearance and on the sites of degradation of LDL in which varying degrees of glucosylation had been achieved. In normal chow-fed animals, the plasma clearance of glcLDL was retarded in proportion to the extent of lysine derivatization. In contrast, in immunized animals the clearance of glcLDL was greatly accelerated. When 10% or more of lysine residues were derivatized, clearance of glcLDL was accelerated 50- to 100-fold. Even when only 5% of lysines were derivatized, plasma clearance was accelerated 2- to 3-fold. Cholesterol feeding inhibited LDL clearance from plasma and decreased LDL uptake of LDL receptor-rich tissues. In a similar manner, glucosylation of LDL inhibited its ability to bind to the LDL receptor and redirected sites of LDL degradation away from LDL receptor-rich tissues. Thus degradation of glcLDL by liver and adrenal was markedly diminished. The presence of antibodies to glcLDL also redirected sites of degradation of the modified LDL, primarily to the reticuloendothelial cells of the liver. There was no evidence for specific targeting of glcLDL-immunoglobulin complexes to the aorta; instead they were targeted to the liver. These data suggest that the presence of humoral antibodies to modified LDL acts to rapidly remove such LDL from plasma and specifically targets such complexes to reticuloendothelial cells, primarily in the liver. In this manner such antibodies may serve a useful purpose.

MeSH Terms
Adrenal Glands/metabolism Animals Aorta/metabolism Autoantibodies/analysis Binding Sites Cholesterol, Dietary/metabolism Glycation End Products, Advanced Immunization Lipoproteins, LDL/immunology,metabolism Liver/metabolism Metabolic Clearance Rate Rabbits Spleen/metabolism
Chemicals
Autoantibodies Cholesterol, Dietary Glycation End Products, Advanced Lipoproteins, LDL glycated lipoproteins, LDL
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wiklund O
Department of Medicine, University of California, San Diego, La Jolla 92093.
Witztum J L
Carew T E
Pittman R C
Elam R L
Steinberg D
Article Info
Journal
Journal of lipid research
Abbr.
J Lipid Res
ISSN
0022-2275
Published
1987-09-00
Pages
1098-109
Language
English
Region
United States
NLM ID
0376606
Subset
IM
Grants
NHLBI NIH HHS · HL-14197 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com