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Immuno-stimulating Activities of Polysaccharide Fractions Isolated from Persimmon Leaves

감잎에서 분리한 다당의 면역자극 활성

  • 신영아 (경기대학교 대학원 대체의학과) ;
  • 박혜령 (경기대학교 식품생물공학과) ;
  • 홍희도 (한국식품연구원) ;
  • 신광순 (경기대학교 식품생물공학과)
  • Received : 2012.11.10
  • Accepted : 2012.11.28
  • Published : 2012.12.31

Abstract

In order to develop new physiologically active polysaccharides from persimmon leaves, two different crude polysaccharides were prepared using hot water (PLW-0) and pectinase digestion (PLE-0) and their immuno-stimulating activities were estimated. PLW-0 and PLE-0 showed similar sugar compositions with 15 different sugars, including rarely observed sugars in general polysaccharides such as 2-O-methyl-fucose, 2-O-methyl-xylose, apiose, aceric acid, 3-deoxy-D-manno-2-octulosonic acid, and 3-deoxy-D-lyxo-2-heptulosaric acid, but the uronic acid content of PLE-0 was lower than that of PLW-0 caused by pectinase treatment. Both PLW-0 and PLE-0 showed potent anti-complementary activity in a dose-dependent manner which was similar to a known immuno-stimulating polysaccharide, PSK, from Coriolus versicolor. The activity of PLE-0 at a low concentration ($100{\mu}g/m{\ell}$) was higher than that of PLW-0. In an in vitro cytotoxicity analysis, PLW-0 and PLE-0 (up to $1,000{\mu}g/m{\ell}$) did not affect the growth of peritoneal macrophages and Colon 26-M3.1 carcinoma cells. In contrast, they enhanced lymphocyte proliferation activity. Peritoneal macrophages stimulated with PLW-0 and PLE-0 produced various cytokines, such as IL-6 and IL-12. However, PLE-0 was more effective on the cytokine production. Intravenous administration of PLW-0 and PLE-0 significantly augmented natural killer (NK) cell cytotoxicity against Yac-1 tumor cells 3 days after the treatment of polysaccharide fractions. But NK cells obtained from the PLE-treated group showed higher tumoricidal activity even at a low dose of $40{\mu}g$/mouse. In experimental lung metastasis of Colon 26-M3.1 carcinoma cells, prophylactic administration of PLW-0 and PLE-0 significantly inhibited lung metastasis in a dose-dependent manner and PLE-0 was more effective on the inhibition of cancer metasasis. The results lead us to conclude that the pectinase-treated process is indispensable to preparing polysaccharides with higher immune-stimulating activity from persimmon leaves.

Keywords

References

  1. An BJ, Kwak JH, Park JM, Lee JY, Park TS, Lee JT, Son JH, Jo C, Byun MW. 2005. Inhibition of enzyme activities and the antiwrinkle effect of polyphenol isolated from the persimmon leaf (Diospyros kaki) on human skin. Derm Surg 31:848-855
  2. Aspinall GO. 1973. Biogenesis of Plant Cell Wall Polysaccharides. Academic Press, New York, USA. pp. 95-115
  3. Blumenkarntz N, Asboe-Hansen G. 1973. New method for quantitative determination of uronic acid. Anal Biochem 54:484- 489 https://doi.org/10.1016/0003-2697(73)90377-1
  4. Bradford MM. 1976. A rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254 https://doi.org/10.1016/0003-2697(76)90527-3
  5. Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F. 1956. Colorimetric method for determination of sugars and related substances. Anal Chem 28:350-356 https://doi.org/10.1021/ac60111a017
  6. Gorinstein S, Zachwjeja Z, Folta M, Barton H, Plotrowicz J, Zemser M, Welsz M, Trakhtenberg S, Martin-Belloso O. 2001. Comparative contents of dietary fiber, total phenolics, and minerals in persimmons and apples. J Agr Food Chem 49:952-957 https://doi.org/10.1021/jf000947k
  7. Gorinstein S, Zensler M, Wietz M, Halvey S, Bartnikowska E. 1994. Fluorometric analysis of phenolics in persimmon. Biosci Biotechnol Biochem 58:1078-1092
  8. Hong HD. 2011. New technology-immunoregulatory actions of polysaccharides from natural plant resources. Bull Food Technol 24:390-409
  9. Hunter CA, Chizzonite R, Remington JS. 1995. IL-1 beta is required for IL-12 to induce production of IFN-gamma by NK cells. A role for IL-1 beta in the T cell-independent mechanism of resistance against intracellular pathogens. J Immunol 155:4347-4354
  10. Jeong JH, Lee JM, Lee CH, Cho JH, Jang JB, Lee KS. 2009. Anti-tumor metastatic effect and activation of innate immunity by extract of Mori radicis cortex. J Orient Obst Gyn 22: 31-40
  11. Jones TM, Albersheim P. 1972. A gas chromatography method for the determination of aldose and uronic acid constituents of plant cell wall polysaccharide. Plant Physiol 49:926-936 https://doi.org/10.1104/pp.49.6.926
  12. Jung UJ, Lee JS, Bok SH, Choi MS. 2011. Effects of extracts of persimmon leaf, buckwheat leaf, and Chinese matrimony vine leaf on body fat and metabolism in rats. J Korean Soc Food Sci Nutr 40:1215-1226 https://doi.org/10.3746/jkfn.2011.40.9.1215
  13. Jung WY, Jeong JM. 2012. Change of antioxidative at different harvest time and improvement of atopic dermatitis effects for persimmon leaf extract. Kor J Herbology 27:41-49 https://doi.org/10.6116/kjh.2012.27.1.41
  14. Kabat EA, Mayer MM. 1971. Experimental Immunochemistry. Thormas Publisher. Illinois. USA. pp. 133-240
  15. Kadhim S, Penney C, Lagraoui M, Heibein J, Attardo G, Zacharie B, Connolly T, Gagnon L. 2000. Synergistic anti-tumor activity of a novel immunodulator, BCH-1393, in combination with cyclophosphamide. Int J Immunopharmacol 22:659-671 https://doi.org/10.1016/S0192-0561(00)00028-X
  16. Kantakamalakul W, Jaroenpool J, Pattanapanyasat K. 2003. A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity. J Immunol Methods 272:189-197 https://doi.org/10.1016/S0022-1759(02)00505-7
  17. Karkhanis YD, Zeltner JY, Jackson JJ, Carlo DJ. 1978. A new and improved microassay to determine 2-keto-3-deoxyoctonate in lipopolysaccharide of gram-negative. Anal Biochem 85: 595-601 https://doi.org/10.1016/0003-2697(78)90260-9
  18. Kawakami K, Aketa S, Sakai H, Watanabe Y. 2011. Antihypertensive and vasorelaxant effects of water-soluble proanthocyanidins from persimmon leaf tea in spontaneously hypertensive rats. Biosci Biotechnol Biochem 75:1435-1439 https://doi.org/10.1271/bbb.100926
  19. Keller R, Keist R, Wechsler A, Leist PT, van der Meide PH. 1990. Mechanism of macrophage-mediated tumor cell killing: a comparative analysis of the roles of reactive nitrogen intermediates and tumor necrosis factor. Int J Cancer 46: 682-686 https://doi.org/10.1002/ijc.2910460422
  20. Kim HJ, Kim MK. 2003. Anticancer effect of persimmon leaf extracts on Korean gastric cancer cell. Korean J Nutr 36:133-146
  21. Ko HS, Park MN, Kim BE, Yoon TJ, Song HS, Cho SY, Lee HJ, Jeong SJ, Lee EO, Kim SH. 2010. Anti-metastatic activity of water extract of Samuikoeuiang via enhancement of natural killer cells. J Kor Trad Oncology 15:29-36
  22. Lasek W, Feleszko W, Golab J, Stoklosa T, Marczak M, Dabrowska A, Melejczyk M, Jakobisiak M. 1997. Antitumor effects of the combination immunotherapy with interleukin-12 and tumor necrosis factor alpha in mice. Cancer Immunol Immunother 45:100-108 https://doi.org/10.1007/s002620050408
  23. Lee SJ, Saiki I, Hayakawa Y, Nunome S, Yamada H, Kim SH. 2003. Antimetastatic and immunomodulating properties of a new herbal prescription, Bojung-bangam-tang. Int Immunopharmacol 3:147-157 https://doi.org/10.1016/S1567-5769(02)00091-7
  24. Moon SH, Kim KH, Park KY. 1996. Antitumor effect of persimmon leaves in vivo using Sarcoma-180 cells. J Kor Soc Food Sci Nutr 25:865-870
  25. Moon SH. 2002. Inhibitory effect of persimmon leaves on the mutagenicity in spore rec assay and on the growth of human cancer cells. Korean J Food Nutr 15:23-28
  26. Nathan CF, Murray HW, Cohen ZA. 1980. Current concepts: the macrophage as an effector cell. N Engl J Med 303:662-665 https://doi.org/10.1056/NEJM198009183031202
  27. Parham P. 2009. The Immune System. Garland Science Press. New York. USA. pp. 17-49
  28. Rosenberg SA, Yang JC, Restifo NP. 2004. Cancer immunotherapy: moving beyond current vaccines. Nat Med 10:909- 915 https://doi.org/10.1038/nm1100
  29. Shida K, Suzuki T, Kiyoshima-Shibata J, Shimada S, Nanno M. 2006. Essential roles of monocytes in stimulating human peripheral blood mononuclear cells with Lactobacillus casei to produce cytokine and augment natural killer cell activity. Clin Vaccine Immunol 13:997-1003 https://doi.org/10.1128/CVI.00076-06
  30. Stevenson TT, Darvill AG, Albersheim P. 1988. 3-Deoxy-Dlyxo-2-heptulosaric acid, a component of the plant cell-wall polysaccharide rhamnogalacturonan-II. Carbohyd Res 179: 269-288 https://doi.org/10.1016/0008-6215(88)84124-7
  31. Strome SE, Voss S, Wilcox R, Wakefield TL, Tamada k, Files D, Chapoval A, Lu J, Kasperbauer JL, Padly D, Vile R, Gastineau D, Wettstein P, Chen L. 2002. Strategies for antigen loading of dendritic cells to enhance the antitumor immune response. Cancer Res 62:1884-1889
  32. Tsukagoshi S, Hashimoto Y, Fujii G, Kobayashi H, Nomoto K, Orita K. 1984. Krestin (PSK). Cancer Treat Rev 11:131-155
  33. Wang H, Actor JK, Indrigo J, Olsen M, Dasgupta A. 2003. Asian and Siberian ginseng as a potential modulator of immune function: an in vitro cytokine study using mouse macrophages. Clin Chim Acta 327:123-128 https://doi.org/10.1016/S0009-8981(02)00343-1
  34. Yamada H, Ra KS, Kiyohara K, Cyong JC, Otsuka Y. 1989. Structural characterization of an anti-complementary pectic polysaccharide from the roots of Bupleurum falcatum L. Carbohyd Res 189:209-226 https://doi.org/10.1016/0008-6215(89)84098-4
  35. Yoo YC, Saiki I, Sato K, Azuma I. 1994. MDP-Lys(L18), a lipophilic derivative of muramyl dipeptide, inhibits the metastasis of haematogenous and non-haematogenous tumours in mice. Vaccine 12:175-180 https://doi.org/10.1016/0264-410X(94)90057-4
  36. York WS, Darvill AG, Mcneil M, Albershiem P. 1985. 3-Deoxy- D-manno-2-octulosonic acid (KDO) is a component of rhamnogalacturonan-II, a pectic polysaccharide in the primary cell walls of plants. Carbohyd Res 138:109-126 https://doi.org/10.1016/0008-6215(85)85228-9

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