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Effects of hyaluronic acid on macrophage phagocytosis and active oxygen release

  • Inflammation
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Abstract

The effects of hyaluronic acid (HA) on macrophage function, in terms of the phagocytosis of latex beads and superoxide anion and hydrogen peroxide release stimulated by phorbol myristate acetate (PMA), were studied in guinea-pig peritoneal macrophages. Phagocytosis was inhibited in a dose- and molecularweight-dependent manner by HA. The addition of PMA to the culture, at a dose of more than 10 ng ml−1, caused an increase in the release of active oxygens. The release of active oxygens was inhibited by high molecular weight HA (MW 2.02×106, HA-202) in a dose-dependent manner. In cell-free systems, HA-20-2 had a negligible effect in scavenging these active oxygens. Of the three molecular sizes of HA (MW: 0.28×106, 0.98×106 and 2.02×106), HA-202 most strongly inhibited the active oxygen release. These results indicate that high-molecular-weight HA acts directly on macrophages to inhibit phagocytosis and active oxygen formation, which, in turn, ameliorates the progression of chronic inflammation.

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Abbreviations

HA:

hyaluronic acid

FBS:

fetal bovine serum

PMA:

phorbol myristate acetate

SOD:

superoxide dismutase

HBSS:

Hanks' balanced salt solution

PBS(−):

calcium, magnesium-free phosphate-buffered saline

References

  1. R. Snyderman and M. C. Pike,Structure and function of monocytes and macrophages. InArthritis and Allied Conditions, 11th Edition, (ed. Daniel J. McCarty) pp. 306–335, Lea and Febiger, Philadelphia (1989).

    Google Scholar 

  2. P. A. Revell, V. Mayston, P. Lalor and P. Mapp,The synovial membrane in osteoarthritis: A histological study including the characterization of the cellular infiltrate present in inflammatory osteoarthritis using monoclonal antibodies. Ann. Rheum. Dis.47, 300–307 (1988).

    PubMed  Google Scholar 

  3. K. Mayer and J. W. Palmer,The polysaccharide of the vitreous humor. J. Biol. Chem.107, 629–634 (1934).

    Google Scholar 

  4. L. B. Dahl, I. M. Dahl, A. Engström-Laurent and K. Granath,Concentration and molecular weight of sodium hyaluronate in symovial fluid from patients with rheumatoid arthritis and other arthropathies. Ann. Rheum. Dis.44, 817–822 (1985).

    PubMed  Google Scholar 

  5. H. Saari,Oxygen derived free radicals and synovial fluid hyaluronate. Ann. Rheum. Dis.50, 389–392 (1991).

    PubMed  Google Scholar 

  6. H. Akasaka, S. Seto, M. Yanagi, S. Fukushima and T. Mitsui,Industrial production of hyaluronic acid by Streptoccoccus zooepidemicus. J. Soc. Cosmet. Chem. Japan22, 35–42 (1985).

    Google Scholar 

  7. R. B. Johnston, Jr., C. A. Godzic and Z. A. Cohn,Increased superoxide anion production by immunologically activated and chemically elicited macrophages. J. Exp. Med.148, 115–127 (1978).

    PubMed  Google Scholar 

  8. J. Harpe and C. F. Nathan,A semi-automated micro-assay for H 2O2 release by human blood monocytes and mouse peritoneal macrophages. J. Immunol. Meth.78, 323–336 (1985).

    Google Scholar 

  9. M. Bradford,A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal. Biochem.72, 248–254 (1976).

    PubMed  Google Scholar 

  10. J. Schalkwijk, W. B. van den Berg, L. B. A. van de Putte and L. A. B. Joosten,Hydrogen peroxide suppresses the proteoglycan synthesis of intact articular cartilage. J. Rheumatol.12, 205–210 (1985).

    PubMed  Google Scholar 

  11. E. J. Bates, D. A. Lowther and C. J. Handley,Oxygen freeradicals mediate an inhibition of proteoglycan synthesis in cultured articular cartilage. Ann. Rheum. Dis.43, 462–469 (1984).

    PubMed  Google Scholar 

  12. E. J. Bates, D. A. Lowther and C. C. Johnson,Hyaluronic acid synthesis in articular cartilage: An inhibition by hydrogen peroxide. Biochem. Biophys. Res. Commun.132, 714–720 (1985).

    PubMed  Google Scholar 

  13. P. Merry, P. G. Winyard, C. J. Morris, M. Grootveld and D. R. Blake,Oxygen free radicals, inflammation, and synovitis: The current status. Ann. Rheum. Dis.48, 864–870 (1989).

    PubMed  Google Scholar 

  14. M. S. Baker, J. Feigan and D. A. Lowther,The mechanism of chondrocyte hydrogen peroxide damage. Depletion of intracellular ATP due to suppression of glycolysis caused by oxidation of glycelaldehyde-3-phosphate dehydrogenase. J. Rheumatol.16, 7–14 (1989).

    PubMed  Google Scholar 

  15. J. V. Forrester and E. A. Balazs,Inhibition of phagocytosis by high molecular weight hyaluronate. Immunology40, 435–446 (1980).

    PubMed  Google Scholar 

  16. R. B. Johnson Jr., J. E. Lehmeyer and L. A. Guthrie,Generation of superoxide anion and chemiluminescence by human monocytes during phagocytosis and on contact with surface bound immunoglobulin G. J. Exp. Med.143, 1551–1556 (1976).

    PubMed  Google Scholar 

  17. M. Sasada, A. Kudo, T. Nishimura, T. Kakita, T. Moriguchi, K. Yamamoto and H. Uchino,Candidacidal activity of monocyte-derived human macrophages: Relationship between candida killing and oxygen radical generation by human macrophages. J. Leukoc. Biol.41, 289294 (1987).

    Google Scholar 

  18. M. S. Baker, S. P. Green and D. A. Lowther,Changes in the viscosity of hyaluronic acid after exposure to a myeloperoxidase-derived oxidant. Arth. Rheum.32, 461–467 (1989).

    Google Scholar 

  19. H. Sato, T. Takahashi, H. Ide, T. Fukushima, M. Tabata, F. Sekine, K. Kobayashi, M. Negishi and Y. Niwa,Antioxidant activity of synovial fluid, hyaluronic acid, and two subcomponents of hyaluronic acid. Arth. Rheum.31, 63–71 (1988).

    Google Scholar 

  20. C. B. Underhill,The interaction of hyaluronate with the cell surface: The hyaluronate receptor and the core protein. In The Biology of Hyaluronan, Ciba Foundation Symposium 143, pp. 87–106. Wiley, Chichester 1989.

    Google Scholar 

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Suzuki, Y., Yamaguchi, T. Effects of hyaluronic acid on macrophage phagocytosis and active oxygen release. Agents and Actions 38 (Suppl 1), 32–37 (1993). https://doi.org/10.1007/BF02027210

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