Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Subendothelial retention of atherogenic lipoproteins in early atherosclerosis

Abstract

Complications of atherosclerosis are the most common cause of death in Western societies1. Among the many risk factors identified by epidemiological studies, only elevated levels of lipoproteins containing apolipoprotein (apo) B can drive the development of atherosclerosis in humans and experimental animals even in the absence of other risk factors2. However, the mechanisms that lead to atherosclerosis are still poorly understood. We tested the hypothesis that the subendothelial retention of atherogenic apoB-containing lipoproteins is the initiating event in atherogenesis3. The extracellular matrix of the subendothelium, particularly proteoglycans, is thought to play a major role in the retention of atherogenic lipoproteins4. The interaction between atherogenic lipoproteins and proteoglycans involves an ionic interaction between basic amino acids in apoB100 and negatively charged sulphate groups on the proteoglycans5. Here we present direct experimental evidence that the atherogenicity of apoB-containing low-density lipoproteins (LDL) is linked to their affinity for artery wall proteoglycans. Mice expressing proteoglycan-binding-defective LDL developed significantly less atherosclerosis than mice expressing wild-type control LDL. We conclude that subendothelial retention of apoB100-containing lipoprotein is an early step in atherogenesis.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Distribution of cholesterol.
Figure 2: Effect on aorta of an atherogenic diet in transgenic mice.
Figure 3: Plate-assay analysis of the ability of recombinant LDL to interact with biglycan.

Similar content being viewed by others

References

  1. Ross, R. Cell biology of atherosclerosis. Annu. Rev. Physiol. 57, 791–804 (1995)

    Article  CAS  Google Scholar 

  2. Glass, C. K. & Witztum, J. L. Atherosclerosis. The Road Ahead. Cell 104, 503–516 (2001)

    Article  CAS  Google Scholar 

  3. Williams, K. J. & Tabas, I. The response-to-retention hypothesis of early atherogenesis. Arterioscler. Thromb. Vasc. Biol. 15, 551–561 (1995)

    Article  CAS  Google Scholar 

  4. Srinivasan, S. R. et al. Low density lipoprotein retention by aortic tissue. Contribution of extracellular matrix. Atherosclerosis 62, 201–208 (1986)

    Article  CAS  Google Scholar 

  5. Boren, J. et al. Identification of the principal proteoglycan-binding site in LDL. A single-point mutation in apo-B100 severely affects proteoglycan interaction without affecting LDL receptor binding. J. Clin. Invest. 101, 2658–2664 (1998)

    Article  CAS  Google Scholar 

  6. Boren, J. et al. Identification of the low density lipoprotein receptor-binding site in apolipoprotein B100 and the modulation of its binding activity by the carboxyl terminus in familial defective apo-B100. J. Clin. Invest. 101, 1084–1093 (1998)

    Article  CAS  Google Scholar 

  7. Weisgraber, K. H. & Rall, S. C. Jr Human apolipoprotein B-100 heparin-binding sites. J. Biol. Chem. 262, 11097–11103 (1987)

    CAS  PubMed  Google Scholar 

  8. Hirose, N., Blankenship, D. T., Krivanek, M. A., Jackson, R. L. & Cardin, A. D. Isolation and characterization of four heparin-binding cyanogen bromide peptides of human plasma apolipoprotein B. Biochemistry 26, 5505–5512 (1987)

    Article  CAS  Google Scholar 

  9. Camejo, G., Olofsson, S. O., Lopez, F., Carlsson, P. & Bondjers, G. Identification of Apo B-100 segments mediating the interaction of low density lipoproteins with arterial proteoglycans. Arteriosclerosis 8, 368–377 (1988)

    Article  CAS  Google Scholar 

  10. Yao, Z. et al. Elimination of apolipoprotein B48 formation in rat hepatoma cell lines transfected with mutant human apolipoprotein B cDNA constructs. J. Biol. Chem. 267, 1175–1182 (1992)

    CAS  PubMed  Google Scholar 

  11. Goldberg, I. J. et al. The NH2-terminal region of apolipoprotein B is sufficient for lipoprotein association with glycosaminoglycans. J. Biol. Chem. 273, 35355–35361 (1998)

    Article  CAS  Google Scholar 

  12. Simionescu, M. & Simionescu, N. Endothelial transport of macromolecules: transcytosis and endocytosis. A look from cell biology. Cell Biol. Rev. 25, 5–78 (1991)

    CAS  PubMed  Google Scholar 

  13. Tangirala, R. K., Rubin, E. M. & Palinski, W. Quantitation of atherosclerosis in murine models: Correlation between lesions in the aortic origin and in the entire aorta, and differences in the extent of lesions between sexes in LDL receptor-deficient and apolipoprotein E-deficient mice. J. Lipid Res. 36, 2320–2328 (1995)

    CAS  PubMed  Google Scholar 

  14. Puhl, H., Waeg, G. & Esterbauer, H. Methods to determine oxidation of low-density lipoproteins. Methods Enzymol. 233, 425–441 (1994)

    Article  CAS  Google Scholar 

  15. Yagi, K. A simple fluorometric assay for lipoperoxide in blood plasma. Biochem. Med. 15, 212–216 (1976)

    Article  CAS  Google Scholar 

  16. Ji, Z. S., Pitas, R. E. & Mahley, R. W. Differential cellular accumulation/retention of apolipoprotein E mediated by cell surface heparan sulfate proteoglycans. Apolipoproteins E3 and E2 greater than E4. J. Biol. Chem. 273, 13452–13460 (1998)

    Article  CAS  Google Scholar 

  17. Brissette, L., Roach, P. D. & Noel, S. P. The effects of liposome-reconstituted apolipoproteins on the binding of rat intermediate density lipoproteins to rat liver membranes. J. Biol. Chem. 261, 11631–11638 (1986)

    CAS  PubMed  Google Scholar 

  18. Milne, R. W., Theolis, R. Jr, Verdery, R. B. & Marcel, Y. L. Characterization of monoclonal antibodies against human low density lipoprotein. Arteriosclerosis 3, 23–30 (1983)

    Article  CAS  Google Scholar 

  19. Purcell-Huynh, D. A. et al. Transgenic mice expressing high levels of human apolipoprotein B develop severe atherosclerotic lesions in response to a high-fat diet. J. Clin. Invest. 95, 2246–2257 (1995)

    Article  CAS  Google Scholar 

  20. Nicoletti, A., Kaveri, S., Caligiuri, G., Bariety, J. & Hansson, G. K. Immunoglobulin treatment reduces atherosclerosis in apo E knockout mice. J. Clin. Invest. 102, 910–918 (1998)

    Article  CAS  Google Scholar 

  21. Mahley, R. W. et al. Inhibition of lipoprotein binding to cell surface receptors of fibroblasts following selective modification of arginyl residues in arginine-rich and B apoproteins. J. Biol. Chem. 252, 7279–7287 (1977)

    CAS  PubMed  Google Scholar 

  22. Ohlsson, B. G. et al. Oxidized low density lipoprotein inhibits lipopolysaccharide-induced binding of nuclear factor-kappaB to DNA and the subsequent expression of tumour necrosis factor-α and interleukin-1β in macrophages. J. Clin. Invest. 98, 78–89 (1996)

    Article  CAS  Google Scholar 

  23. McFarlane, A. S. Efficient trace-labelling of proteins with iodine. Nature 182, 53 (1958)

    Article  ADS  CAS  Google Scholar 

  24. Hurt-Camejo, E. et al. Effect of arterial proteoglycans and glycosaminoglycans on low density lipoprotein oxidation and its uptake by human macrophages and arterial smooth muscle cells. Arterioscler. Thromb. 12, 569–583 (1992)

    Article  CAS  Google Scholar 

  25. Bligh, E. G. & Dyer, W. J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37, 911–917 (1959)

    Article  CAS  Google Scholar 

  26. Randle, D. H., Zindy, F., Sherr, C. J. & Roussel, M. F. Differential effects of p19Arf and p16Ink4a loss on senescence of murine bone marrow-derived preB cells and macrophages. Proc. Natl Acad. Sci. USA 98, 9654–9659 (2001)

    Article  ADS  CAS  Google Scholar 

  27. Stanley, E. R. The macrophage colony-stimulating factor, CSF-1. Methods Enzymol. 116, 564–587 (1985)

    Article  CAS  Google Scholar 

  28. Schwenke, D. C. Gender differences in intima-media permeability to low-density lipoprotein at atherosclerosis-prone aortic sites in rabbits. Lack of effect of 17 β-estradiol. Arterioscler. Thromb. Vasc. Biol. 17, 2150–2157 (1997)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank L. Lindgren, C. Ullström and A. Lidell for technical assistance, O. Nerman and K. Wiklander for statistical analysis, D. Schwenke for advice with retention studies. K. Weisgraber for comments on the manuscript, and S. Ordway and G. Howard for editorial assistance. This work was supported by the Swedish Medical Research Council, The Swedish Foundation for Strategic Research, The Swedish Heart–Lung Foundation, and in part by a National Institutes of Health grant..

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jan Borén.

Ethics declarations

Competing interests

The authors declare that they have no competing financial interests

Rights and permissions

Reprints and permissions

About this article

Cite this article

Skålén, K., Gustafsson, M., Rydberg, E. et al. Subendothelial retention of atherogenic lipoproteins in early atherosclerosis. Nature 417, 750–754 (2002). https://doi.org/10.1038/nature00804

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nature00804

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing