International Journal of Applied Science and Engineering
Published by Chaoyang University of Technology

Rang Huang and Hui-Ting Lee*

Institute of Oceanography, National Taiwan University, Taipei, Taiwan


 

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ABSTRACT


Seaweeds contain a variety of biologically active substances, which are useful for therapy and medicinal purposes. One of the potent uses has been found in its immune functions. In the present report, we describe immunological properties of the marine brown alga Endarachne binghamiae against murine macrophage and human T cells in vitro. It was observed that various extracts from the alga effectively stimulated cell proliferation and that the stimulation activity of active substances varied with growth habitat of the alga assayed. The reported alga was found rich in polysaccharides. Of which sodium alginate exhibited strong stimulation activity for macrophage and T cell proliferation, and also alginic acid but to a lesser extent. A glycoprotein isolated from the reported alga was also a strong proliferation stimulant. Additionally, it significantly induced the production of TNF-αand nitric oxide by macrophages and IFN-γby T cells in a concentration-dependent manner. These assay results suggested that alginate and protein of the reported alga could be promising immune stimulants and modulants.


Keywords: marine algae; sodium alginate; protein; proliferation stimulation; Cytokines.


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REFERENCES


  1. [1] A.O.A.C. 1995. “Official Methods of Analysis”. Association of Official Analytical Chemists. Washington, D.C.

  2. [2] Dubois, M., Gilles, K.-A., Hamilton, J.-K., Robers, P.-A. and Smith, F. 1956. Colorimetric method for determination of sugars and related substances. Analytical Chemistry, 28: 350-356.

  3. [3] Hoppe, H.A. 1979. Marine algae and their products and constituents in pharmacy. In: Marine Algae in Pharmaceutical Science, edited by H.A. Hoppe, T. Levring, and Y. Tanaka. Walter de Gruyter, Berlin: 25-119.

  4. [4] Hori, K., Ikegami, S., Miyazawa, K. and Ito, K. 1988. Mitogenic and antineoplastic isoaggluinins from the red alga Solieria robusta. Physiochemistry, 27: 2063-2067.

  5. [5] Hudson, J.-B., Kim, J.-H., Lee, M.-K., DeWreede, R.-E. and Hong, Y.-K. 1999. Anti-viral compounds in extracts of Ko-rean seaweeds; Evidence for multiple activities. Journal of Applied Phycology, 10: 427-434.

  6. [6] Kawakubo, A., Makino, H., Ohnishi, J.-I., Hirohara, H. and Hori, K. 1997. The marine red alga Eucheuma serra J. Agardh, a high yielding source of two isolectins. Journal of Applied Phycology, 9: 331-338.

  7. [7] Liao, W.-R., Lin, J.-Y., Shieh, W.-Y. and Huang, R. 2003. Antibiotic activity of lectins from marine algae against marine vibrios. Journal of Industrial Microbiology & Biotechnology, 30: 433-439.

  8. [8] Lima, H.-C., Costa, F.-H.-F., Sampaio, A.-H., Neves, S.-A., Benevides, N.-M.-B., Teixeira, D.-I.-A., Rogers, D.-J. and Freitas, A.-L.-P. 1998. Induction and inhibition of human lymphocyte transformation by the lectin from the red marine alga Amansia multifida. Journal of Applied Phycology, 10: 153-162.

  9. [9] Mossman, R. 1983. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. Journal of Immunological Methods, 65: 55-63.

  10. [10] Nika, K., Mulloy, B., Carpenter, B. and Gibbs, R. 2003. Specific recognition of immune cytokines by sulphated polysaccharides from marine algae. European Journal of Phycology, 38: 257-264.

  11. [11] Okai, Y., Okai, K.-H., Ishizaka, S. and Yamashita, U. 1997. Enhancing effect of polysaccharides from an edible brown alga, Hizikia fusiforme (Hiziki), on release of tumor necrosis factor–αfrom macrophages of endotoxin-nonresponder C3H/HeJ mice. Nutrition and Cancer, 27: 74-79.

  12. [12] Otterlei, M., Ostgaard, K., Skjak-Braek, G., Smidsrod, O., Soon-Shiong, P. and Espevik, T. 1991. Induction of cytokine production from human monocytes stimulated with alginate. Journal of Immunotherapy, 10: 286-291.

  13. [13] Seljelid, R., Figenschau, Y., Bogwald, J. Rasmussen, L.-T. and Austgulen, R.-E. 1989. Evidence that tumor necrosis induced by aminated beta 1-3D polyglucose is mediated by a concerted action of local and systemic cytokines. Scand. Journal of Immunology, 30: 687-94.

  14. [14] Shan, B.-E., Yoshida, Y., Kuroda, E. and Yamashita, U. 1999. Immunomodulating activity of seaweed extract on human lymphocytes in vitro. International Journal of Immunopharmacology, 21: 59-70.

  15. [15] Son, E.-H., Moon, E.-Y., Rhee, D.-K. and Pyo, S. 2001. Stimulation of various functions in murine peritoneal macrophages by high manuronic acid-containing alginate (HMA) exposure in vivo. International Journal of Immunopharmacology, 1: 147-154.

  16. [16] Whyte, J.-N.-C. 1988. Extraction of alginic acid from a brown seaweed. In: Experimental Phycology- A Laboratory Manual, edited by C.S. Lobban, D.J. Chapman and B.P. Kremer. Cambridge University Press: 168-173.

  17. [17] Yamamoto, I., Takahashi, M., Tamura, E. and Maruyama, H. 1982. Antitumor activity of crude extracts from edible marine algae against L-1210 Leukemia. Botanica Marina, 25: 455-457.

  18. [18] Yoshizawa, Y., Enomoto, A., Todho, H., Ametani, A. and Kaminogawa, S. 1993. Activation of murine macrophages by polysaccharide fractions from marine alga (Porphyra yezoensis). Bioscience Biotechnology Biochemistry, 57: 1862-1866.


ARTICLE INFORMATION




Accepted: 2005-03-03
Available Online: 2005-12-13


Cite this article:

Huang, R., Lee, H.-T. 2005. Immunological properties of the marine brown alga endarachne binghamiae (Phaeophyceae). International Journal of Applied Science and Engineering, 3, 167–173. https://doi.org/10.6703/IJASE.2005.3(3).167