Abstract

Fucoidans are sulfated polysaccharides capable of exerting biological activities such as antitumor and immunomodulatory effects. Previous studies demonstrated the antitumor activity of non-cytotoxic fucoidans from the seaweed Dictyota caribaea (Dc-SP) in vivo. Macrophages (Mfs) are innate immune cells capable of promoting or inhibiting tumor growth depending on the stimulus. This study aimed to evaluate the immunostimulant activity of Dc-SP on a murine Mfs cell line (RAW 264.7) in vitro. Dc-SP was assessed for its ability to modify cell viability and stimulate the production of antitumor markers on RAW 264.7 cells. Dc-SP induced an increase (p < 0.05) in the production of NO and cytokines TNF-α, IL-1β, and IL-10. The exposure of RAW 264.7 to Dc-SP also increased (p < 0.05) the expression of M1 phenotype markers such as iNOS, CD86, and MHC II. Dc-SP did not exhibit direct cytotoxicity on a murine melanoma cell line (B16–F10). However, the conditioned medium (CM) obtained from RAW 264.7 previously stimulated with Dc-SP (CM-Dc-SP) showed antiproliferative activity on tumor cells. B16–F10 incubated with CM-Dc-SP showed a cytostatic profile, tumor cells did not alter membrane integrity, however, they suffered morphological changes such as cell shrinkage and high granularity. In conclusion, Dc-SP stimulated RAW 264.7 to an antitumor phenotype.

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