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Immolina, a High–Molecular-Weight Polysaccharide Fraction of Spirulina, Enhances Chemokine Expression in Human Monocytic THP-1 Cells

Reinhard Grzanna, Anna Polotsky, Phong V. Phan, Nirmal Pugh, David Pasco, Carmelita G. Frondoza
2006 Journal of Alternative and Complementary Medicine  
Spirulina (Spirulina platensis) is a dietary supplement valued for its immune-enhancing properties. We previously reported that the immunostimulatory effect of spirulina can be traced to a high-molecular-weight polysaccharide fraction. This fraction, labeled Immolina, activates nuclear factor kappa-B in human monocytic THP-1 cells and increases expression of proinflammatory cytokines. Objective: To characterize further the immunostimulatory effects of Immolina on THP-1 cells, we evaluated its
more » ... we evaluated its effect on genes encoding the chemokines interleukin (IL)-8, MCP-1, MIP-1␣, MIP-1␤, IP-10, the cytokines tumor necrosis factor (TNF)-␣, IL-1␤, and the enzyme cyclo-oxygenase-2 (COX-2). Methods: THP-1 cells were exposed to concentrations of Immolina ranging from 1 ng/mL to 100 g/mL and changes in gene expression were assessed by reverse transcriptase-polymerase chain reaction (RT-PCR). For comparison, THP-1 cells were activated with 1 ng/mL of TNF-␣, 10 ng/mL of IL-1␤, or 10 ng/mL of lipopolysaccharide using the same assay conditions. To assess the response of THP-1 cells to Immolina at the protein level, we probed culture supernatants using a cytokine array immunoblot assay. Results: RT-PCR analysis revealed that Immolina dose-dependently increased the expression of all 5 chemokines tested as well as the expression of TNF-␣, IL-1␤, and COX-2. The cytokine array immunoblot assay revealed an increase in the chemokines IL-8 and MIP-1␤. Thymidine uptake experiments verified that Immolina did not affect the viability and growth rate of THP-1 cells. Conclusions: The results of the experiments demonstrate that Immolina activates THP-1 cells in a manner that is consistent with the recruitment of diverse populations of leukocytes in response to inflammatory and infectious signals.
doi:10.1089/acm.2006.12.429 pmid:16813506 fatcat:jnizvwd6f5gu3gomxludludy6q