In an in vitro model system using isolated human granulocytes high molecular weight hyaluronic acid stimulated the initial rate of phagocytosis of complement-opsonized latex particles. This specific quality was dependent on the molecular size and occurred at low concentrations (1-10 mg/l) of hyaluronic acid. However, at high concentrations (> 100 mg/l) hyaluronic acid inhibited the initial rate of phagocytosis of both IgG- and complement-opsonized particles. The latter effect was shared with chrondoitin sulphate, heparan sulphate and heparin. The results suggest that hyaluronic acid may be instrumental in controlling inflammatory processes.
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Håkansson et al. (1980) studied this question.
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