Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1995 Jul 15;309(Pt 2):461–464. doi: 10.1042/bj3090461

Serum amyloid A protein enhances the activity of secretory non-pancreatic phospholipase A2.

W Pruzanski 1, F C de Beer 1, M C de Beer 1, E Stefanski 1, P Vadas 1
PMCID: PMC1135754  PMID: 7542869

Abstract

The acute-phase proteins serum amyloid A protein (SAA) and secretory phospholipase A2 (sPLA2) are simultaneously expressed during inflammatory conditions. SAA associates with high-density lipoprotein (HDL) altering its physicochemical composition. We found that purified acute-phase SAA, but not the constitutive form, markedly enhances the lipolytic activity of sPLA2 in a dose-related manner with phosphatidylcholine/lysophosphatidylcholine or phosphatidylethanolamine/lysophosphatidylethanolamine liposomal substrates. Normal HDL was found to reduce activity of sPLA2 in a dose-dependent manner, but when acute-phase HDL containing 27% SAA was tested, it enhanced sPLA2 activity. Immunopurified monospecific antibodies against SAA completely abolished the enhancing activity of SAA and acute-phase HDL. Given the central role of HDL in lipoprotein metabolism, the interaction between HDL, SAA and sPLA2 may account for changes detected in lipoprotein metabolism during the acute phase.

Full text

PDF
461

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bamberger M., Glick J. M., Rothblat G. H. Hepatic lipase stimulates the uptake of high density lipoprotein cholesterol by hepatoma cells. J Lipid Res. 1983 Jul;24(7):869–876. [PubMed] [Google Scholar]
  2. Bamberger M., Lund-Katz S., Phillips M. C., Rothblat G. H. Mechanism of the hepatic lipase induced accumulation of high-density lipoprotein cholesterol by cells in culture. Biochemistry. 1985 Jul 2;24(14):3693–3701. doi: 10.1021/bi00335a044. [DOI] [PubMed] [Google Scholar]
  3. Cabana V. G., Siegel J. N., Sabesin S. M. Effects of the acute phase response on the concentration and density distribution of plasma lipids and apolipoproteins. J Lipid Res. 1989 Jan;30(1):39–49. [PubMed] [Google Scholar]
  4. Coetzee G. A., Strachan A. F., van der Westhuyzen D. R., Hoppe H. C., Jeenah M. S., de Beer F. C. Serum amyloid A-containing human high density lipoprotein 3. Density, size, and apolipoprotein composition. J Biol Chem. 1986 Jul 25;261(21):9644–9651. [PubMed] [Google Scholar]
  5. Collet X., Perret B. P., Simard G., Vieu C., Douste-Blazy L. Behaviour of phospholipase-modified HDL towards cultured hepatocytes. I. Enhanced transfers of HDL sterols and apoproteins. Biochim Biophys Acta. 1990 Apr 17;1043(3):301–310. doi: 10.1016/0005-2760(90)90031-r. [DOI] [PubMed] [Google Scholar]
  6. De Beer F. C., Mallya R. K., Fagan E. A., Lanham J. G., Hughes G. R., Pepys M. B. Serum amyloid-A protein concentration in inflammatory diseases and its relationship to the incidence of reactive systemic amyloidosis. Lancet. 1982 Jul 31;2(8292):231–234. doi: 10.1016/s0140-6736(82)90321-x. [DOI] [PubMed] [Google Scholar]
  7. Godenir N. L., Jeenah M. S., Coetzee G. A., Van der Westhuyzen D. R., Strachan A. F., De Beer F. C. Standardisation of the quantitation of serum amyloid A protein (SAA) in human serum. J Immunol Methods. 1985 Nov 7;83(2):217–225. doi: 10.1016/0022-1759(85)90243-1. [DOI] [PubMed] [Google Scholar]
  8. Kisilevsky R., Subrahmanyan L. Serum amyloid A changes high density lipoprotein's cellular affinity. A clue to serum amyloid A's principal function. Lab Invest. 1992 Jun;66(6):778–785. [PubMed] [Google Scholar]
  9. Liao F., Andalibi A., deBeer F. C., Fogelman A. M., Lusis A. J. Genetic control of inflammatory gene induction and NF-kappa B-like transcription factor activation in response to an atherogenic diet in mice. J Clin Invest. 1993 Jun;91(6):2572–2579. doi: 10.1172/JCI116495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Malle E., Steinmetz A., Raynes J. G. Serum amyloid A (SAA): an acute phase protein and apolipoprotein. Atherosclerosis. 1993 Sep;102(2):131–146. doi: 10.1016/0021-9150(93)90155-n. [DOI] [PubMed] [Google Scholar]
  11. Meek R. L., Urieli-Shoval S., Benditt E. P. Expression of apolipoprotein serum amyloid A mRNA in human atherosclerotic lesions and cultured vascular cells: implications for serum amyloid A function. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3186–3190. doi: 10.1073/pnas.91.8.3186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Nakano T., Ohara O., Teraoka H., Arita H. Group II phospholipase A2 mRNA synthesis is stimulated by two distinct mechanisms in rat vascular smooth muscle cells. FEBS Lett. 1990 Feb 12;261(1):171–174. doi: 10.1016/0014-5793(90)80663-4. [DOI] [PubMed] [Google Scholar]
  13. Pruzanski W., Keystone E. C., Sternby B., Bombardier C., Snow K. M., Vadas P. Serum phospholipase A2 correlates with disease activity in rheumatoid arthritis. J Rheumatol. 1988 Sep;15(9):1351–1355. [PubMed] [Google Scholar]
  14. Pruzanski W., Scott K., Smith G., Rajkovic I., Stefanski E., Vadas P. Enzymatic activity and immunoreactivity of extracellular phospholipase A2 in inflammatory synovial fluids. Inflammation. 1992 Oct;16(5):451–457. doi: 10.1007/BF00918971. [DOI] [PubMed] [Google Scholar]
  15. Pruzanski W., Vadas P., Browning J. Secretory non-pancreatic group II phospholipase A2: role in physiologic and inflammatory processes. J Lipid Mediat. 1993 Nov;8(3):161–167. [PubMed] [Google Scholar]
  16. Pruzanski W., Vadas P., Stefanski E., Urowitz M. B. Phospholipase A2 activity in sera and synovial fluids in rheumatoid arthritis and osteoarthritis. Its possible role as a proinflammatory enzyme. J Rheumatol. 1985 Apr;12(2):211–216. [PubMed] [Google Scholar]
  17. Qiao J. H., Castellani L. W., Fishbein M. C., Lusis A. J. Immune-complex-mediated vasculitis increases coronary artery lipid accumulation in autoimmune-prone MRL mice. Arterioscler Thromb. 1993 Jun;13(6):932–943. doi: 10.1161/01.atv.13.6.932. [DOI] [PubMed] [Google Scholar]
  18. Rokita H., Loose L. D., Bartle L. M., Sipe J. D. Synergism of interleukin 1 and interleukin 6 induces serum amyloid A production while depressing fibrinogen: a quantitative analysis. J Rheumatol. 1994 Mar;21(3):400–405. [PubMed] [Google Scholar]
  19. Shephard E. G., de Beer F. C., de Beer M. C., Jeenah M. S., Coetzee G. A., van der Westhuyzen D. R. Neutrophil association and degradation of normal and acute-phase high-density lipoprotein 3. Biochem J. 1987 Dec 15;248(3):919–926. doi: 10.1042/bj2480919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Smith J. W., McDonald T. L. Production of serum amyloid A and C-reactive protein by HepG2 cells stimulated with combinations of cytokines or monocyte conditioned media: the effects of prednisolone. Clin Exp Immunol. 1992 Nov;90(2):293–299. doi: 10.1111/j.1365-2249.1992.tb07945.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Strachan A. F., Shephard E. G., Bellstedt D. U., Coetzee G. A., van der Westhuyzen D. R., de Beer F. C. Human serum amyloid A protein. Behaviour in aqueous and urea-containing solutions and antibody production. Biochem J. 1989 Oct 15;263(2):365–370. doi: 10.1042/bj2630365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Tall A. R. Plasma high density lipoproteins. Metabolism and relationship to atherogenesis. J Clin Invest. 1990 Aug;86(2):379–384. doi: 10.1172/JCI114722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Vadas P., Browning J., Edelson J., Pruzanski W. Extracellular phospholipase A2 expression and inflammation: the relationship with associated disease states. J Lipid Mediat. 1993 Aug;8(1):1–30. [PubMed] [Google Scholar]
  24. Vadas P., Pruzanski W. Induction of group II phospholipase A2 expression and pathogenesis of the sepsis syndrome. Circ Shock. 1993 Feb;39(2):160–167. [PubMed] [Google Scholar]
  25. Vadas P., Schouten B. D., Stefanski E., Scott K., Pruzanski W. Association of hyperphospholipasemia A2 with multiple system organ dysfunction due to salicylate intoxication. Crit Care Med. 1993 Jul;21(7):1087–1091. doi: 10.1097/00003246-199307000-00027. [DOI] [PubMed] [Google Scholar]
  26. Vadas P., Taylor T. E., Chimsuku L., Goldring D., Stefanski E., Pruzanski W., Molyneux M. E. Increased serum phospholipase A2 activity in Malawian children with falciparum malaria. Am J Trop Med Hyg. 1993 Oct;49(4):455–459. doi: 10.4269/ajtmh.1993.49.455. [DOI] [PubMed] [Google Scholar]
  27. Whitehead A. S., de Beer M. C., Steel D. M., Rits M., Lelias J. M., Lane W. S., de Beer F. C. Identification of novel members of the serum amyloid A protein superfamily as constitutive apolipoproteins of high density lipoprotein. J Biol Chem. 1992 Feb 25;267(6):3862–3867. [PubMed] [Google Scholar]
  28. Wolfe F., Mitchell D. M., Sibley J. T., Fries J. F., Bloch D. A., Williams C. A., Spitz P. W., Haga M., Kleinheksel S. M., Cathey M. A. The mortality of rheumatoid arthritis. Arthritis Rheum. 1994 Apr;37(4):481–494. doi: 10.1002/art.1780370408. [DOI] [PubMed] [Google Scholar]
  29. de Beer M. C., Kindy M. S., Lane W. S., de Beer F. C. Mouse serum amyloid A protein (SAA5) structure and expression. J Biol Chem. 1994 Feb 11;269(6):4661–4667. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES