Abstract
The complement system consists of over 20 serum proteins including nine com-plement components (C1 to C9) and their regulators, and is normally present in blood serum in an inactive form. The system is essential for the operation of the innate as well as the adaptive immune defence [1]. The complement proteins can be activated through three cascade pathways: by the classical pathway, by the alternative pathway and by the antibody-independent lectin pathway (Fig. 1). The activation of the classical pathway is initiated by immune complexes containing IgM and IgG antibodies, Cl binds to the Fc region of antibodies through subcomponent Cl q, then the complex activates the further complement system by the cascade mechanism. The alternative pathway is directly activated from C3 by microorganisms, protozoa, or some activators such as lipopolysaccharide through an antibody independent mechanism. Recently, an antibody-independent mannanbinding lectin (MBL) pathway has also been established as the third activation pathway of complement systems [2,3]. This pathway is initiated by the binding of serum MBL (carbohydrate binding component in complement-dependent antibacterial factor, RaRF [4]), which is structurally related to Cl q, to the surface carbohydrates and activated through two MBL-associated serine proteases. The MBL pathway is activated by specific carbohydrate structures of microorganisms including bacteria, yeast, parasitic protozoa and viruses, and exhibits antibacterial activity through killing mediated by the terminal, lytic complement components or by promoting phagocytosis [3].
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Law SKA, Reid KBM (eds) (1995) Complement, 2nd ed. IRL Press, New York, Oxford
Thiel S, Vorup-Jensen T, Stover CM, Schwaeble W, Laursen SB, Paulsen K, Willis AC, Eggleton P, Hamsen S, Holmskov U et al (1997) A second serine protease associated with mannan-binding lectin that activates complement. Nature 386: 506–510
Turner WT (1996) Mannose-binding lectin: the pluripotent molecule of the innate immune system. Immunol Today 17: 532–540
Matsushita M, Takahashi A, Hatsuse H, Kawakami M, Fujita T (1992) Human mannose-binding protein is identical to a component of Ra-reactive factor. Biochem Biophys Res Commun 183: 645–651
Wagner H, Jurcic K (1991) Assays for immunomodulation and effects on mediators of inflammation. Methods in Plant Biochemistry 6: 195–217
Egivang TG, Befus AD (1984) The role of complement in the induction and regulation of immune responses. Immunology 51: 207–224
Okuda T, Yoshioka Y, Ikekawa T, Chihara G, Nishioka K (1972) Anti-complementary activity of anti-tumor polysaccharides. Nature (London) 238: 59–60
Hamuro J, Hadding U, Bitter-Suermann (1978) Solid phase activation of alternative pathway of complement by ß-3,3-glucans and its possible role for tumor regressing activity.Immunol 34: 695–705
Morrison DC, Ulevitch RJ (1978) The effects of bacterial endotoxins on host mediation systems. Am J Path 93: 526–617
Inai S, Nagai K, Ebisu S, Kato K, Kotani S, Misaki A (1976) Activation of the alternative complement pathway by water insoluble glucans of Streptococus mutans: The relation between their chemical structures and activating potencies. J Immunol 117: 1256–1260
Götze O, Müller-Eberhard HJ (1971) The C3-activation system: An alternate pathway of complement activation. J Exp Med 134: 905–1085
Li XY, Nolte R, Vogt W (1983) Natural antibodies against a polysaccharide (BO) from sugar cane mediate its complement -activating effect. Immunobiology 164: 110–117
Pillemer L, Blum L, Lepow IH, Ross OA, Todd EW, Wardlaw AC (1954) The properdin system and immunity I. Demonstration and isolation of new serum protein, properdin and its role in immune phenomenon. Science 120: 279–285
Morrison DC, Kline LF (1977) Activation of the classical and properdin pathways of complement by bacterial lipopolysaccharides (LPS). J Immunol 118: 362–368
Wilson ME, Morrison DC (1982) Evidence for different requirements in physical state for the interaction of lipopolysaccharides with the classical and alternative pathway of complement. Eur J Biochem 128: 137–141
Puhlmann J, Knams U, Tubaro L, Schaefer W, Wagner H (1992) Immunologically active metallic ion-containing polysaccharides of Achyrocline satureioides. Phytochem 31: 2617–2621
Yamada H, Kiyohara H, Cyong JC, Otsuka Y (1985) Studies on polysaccharides from Angelica acutiloba IV. Characterization of anti-complementary arabinogalactan from Angelica acutiloba Kitagawa. Molec Immunol 22: 295–304
Yamada H, Nagai T, Cyong JC, Otsuka Y, Tomoda M, Shimizu N, Shimada K (1985) Relationship between chemical structure and anti-complementary activity of plant polysaccharides. Carbohydr Res 144: 101–111
Yamada H, Ohtani K, Kiyohara H, Cyong JC, Otsuka Y, Ueno Y, Omura S (1985) Purification and chemical properties of anti-complementary polysaccharide from the leaves of Artemisia princeps. Planta Medica 51: 121–125
Yamada H, Otsuka Y, Omura S (1986) Structural characterization of anti-complementary polysaccharides from the leaves of Artemisia princeps PAMP. Planta Medica 52: 311–314
Yamada H, Kiyohara H, Otsuka Y (1987) Further structural studies of an anti-complementary acidic heteroglycan from the leaves of Artemisia princeps. Carbohydr Res 170: 181–191
Yamada H, Yanahira S, Kiyohara H, Cyong JC, Otsuka Y (1986) Water soluble glucans from the seed of Coix lacryma-jobi var. ma-yuen. Phytochem 25: 129–132
Yamada H, Cyong JC, Otsuka Y (1986) Purification and chracterization of complement activating-acidic polysaccharide form the root of Lithospermum euchromum Royle. Int J Immunopharmacol 8: 71–82
Kiyohara H, Yamada H, Cyong JC, Otsuka Y (1986) Molecular aggregation and anti-complementary activity of arabinogalactan from Angelica acutiloba. (Studies on polysaccharides from Angelica acutiloba, part V). J Pharmacobio-Dyn 9: 339–346
Yamada H, Kiyohara H, Cyong JC, Otsuka Y (1987) Structural characterization of an anti-complementary arabinogalactan form the roots of Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba, part VI). Carbohydr Res 159: 275–291
Kiyohara H, Yamada H, Otsuka Y (1987) Unit structure of anti-complementary arabinogalactan form Angelica acutiloba Kitagawa.(Studies on polysaccharides form Angelica acutiloba, part VII).Carbohydr Res 167: 221–237
Kiyohara H, Yamada H (1989) Structure of an anti-complementary arabinogalactan form the root of Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba,Part X). Carbohydr Res 193: 173–192
Yamada H, Yanahira S, Kiyohara H, Cyong JC, Otsuka Y (1987) Characterization of anti-complementary acidic heteroglycans from the seed of Coix lacryma-jobi var. Ma-Yuen. Phytochem 26: 3269–3275
Wagner H, Jordan E (1988) An immunologically active arabinogalactan from Viscus album. Phytocbem 27: 2511–2517
Yamada H, Ra K-S, Kiyohara H, Cyong JC, Yang HC, Otsuka Y (1988) Characterization of anti-complementary neutral polysaccharide from the roots of Bupleurum falcaturn L. Phytocbem 27: 3163–3168
Gao QP, Kiyohara H, Cyong JC, Yamada H (1988) Characterization of anti-complementary acidic heteroglycans from the leaves of Panax ginseng C. A. Meyer. Carbohydr Res 181: 175–187
Gao QP, Kiyohara H, Yamada H (1990) Further structural studies of anti-complementary acidic heteroglycans from the leaves of Panax ginseng C. A. Meyer. Carbohydr Res 196: 111–125
Kiyohara H, Cyong JC, Yamada H (1988) Structure and anti-complementary activity of pectic polysaccharides isolated form the roots of Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba,Part VIII). Carbohydr Res 182: 259–275
Kiyohara H, Yamada H (1989) Structure of neutral carbohydrate side chains in anti-complementary acidic polysaccharides from the roots of Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba,Part IX). Carbohydr Res 187: 255–265
Tomoda M, Gonda R, Shimizu N, Yamada H, (1989) Plant Mucilages. XLII. An anti-complementary mucilages form the leaves of Malva sylvetris var. mauritana. Chem Pharm Bull 37: 3029–3032
Yamada H, Ra KS, Kiyohara H, Cyong JC, Otsuka Y (1989) Structural characterization of an anti-complementary pectic polysaccharide from the roots of Bupleurum falcatum L. Carbohydr Res 189: 209–226
Ra KS, Yamada H, Sung HJ, Cyong JC, Yang H-C (1989) Purification and chemical properties of anti-complementary polysaccharide from Capsici Fructus. J Kor Agr Chem Soc 32: 378–385
Tomoda M, Shimizu N, Gonda R, Kanari M, Yamada H, Hikino H (1989) Anti-com-plementary and hypoglycemic activities of okra-and hibiscus mucilages. Carbohydr Res 190: 323–328
Tomoda M, Shimizu N, Gonda R, Kanari M, Yamada H, Hikino H (1990) Anti-complementary and hypoglycemic activities of the glycans from the seed of Malva verticillata. Planta Medica 56: 168–170
Gonda R, Tomoda M, Kanari M, Shimizu N, Yamada H (1990) Constituents of the seed of Malva verticillata VI. Characterization and immunological activities of a novel acidic polysaccharide. Chem Pharm Bull 38: 2771–2774
Gonda R, Tomoda M, Shimizu N, Yamada H (1990) Structure and anti-complementary activity of an acidic polysaccharide from the leaves of Malva sylvestris var. mauritiana. Carbohydr Res 198: 323–329
Gao QP, Kiyohara H, Cyong JC, Yamada H (1991) Chemical properties and anti-complementary activity of heteroglycans from the leaves of Panax ginseng C. A. Meyer. Planta Medica 57: 132–136
Zhao JF, Kiyohara H, Sun XB, Matsumto T, Cyong JC, Yamada H, Takemoto N, Kawamura H (1991)In vitro immunostimulating polysaccharide fractions from roots of Glycyrrhiza uralensis Fisch. et DC. Phytother Res 5: 206–210
Zhao JF, Kiyohara H, Yamada H, Takemoto N, Kawamura H (1991) Heterogeneity and characterization of mitogenic and anti-Complementary pectic polysaccharides from the roots of Glycyrrhiza uralensis Fisch. et DC. Carbohydr Res 219: 149–172
Hirano M, Matsumoto T, Kiyohara H, Yamada H (1994) Lipopolysaccharide-independent limulus amebocyte lysate activating, mitogenic and anti-complementary activities of pectic polysaccharides from Chinese herbs. Planta Medica 60: 248–252
Puhlmann J, Zenk M, Wagner H (1991) Immunologically active polysaccharides of Arnica montana cell cultures. Phytochem 30: 1141–1145
Zhao Q-C, Kiyohara H, Nagai T, Yamada H (1992) Structure of the complement activating proteoglycan from pilose antler of Cervus nippon Temminck. Carbohydr Res 230: 361–372
Gonda R, Tomoda M, Takada K, Ohara N, Shimizu N (1992) The core structure of ukonan A, a phagocytosis-activating polysaccharide from the rhizome of Curcuma longa,and immunological activities of degradation products. Chem Pharm Bull 40: 990–993
Zhao JF, Kiyohara H, Matsumoto T, Yamada H (1993) Characterisations of anti-complementary acidic polysaccharides from the roots of Lithospermum euchromum Loyle. Phytochem 34: 719–724
Zhao QC, Kiyohara H, Yamada H (1994) Purification and characterisation of anti-complementary neutral polysaccharides from the leaves of Artemisia princeps PAMP. Phytochem 35: 73–77
Wagner H, Willer F, Samtleben R, Boos G (1994) Search for antiprostatic principle of stinging nettle (Urtica dioica) roots. Phytomedicine 1: 213–224
Samuelsen AB, Paulsen BS, Wold JK, Otsuka H, Yamada H, Espevik T (1995) Isolation and partial characterization of biologically active polysaccharides from Plantago major L. Phytotherapy Res 9: 211–21
Samuelsen AB, Paulsen BS, Wold JK, Otsuka H, Kiyohara H, Yamada H, Knutsen SH (1996) Characterization of a biological active pectin from Plantago major L. Carbohydr Polymers 30: 37–44
Zhang YW, Kiyohara H, Matsumoto T, Yamada H (1997) Fractionation and chemical properties of immunomodulating polysaccharides from roots of Dipsacus asperoides. Plant Medica 63: 393–399
Clarke AE, Anderson RL, Stone BA (1979) Form and function of arabinogalactans and arabinogalactan-proteins. Phytochem 18: 521–540
Yamada H, Kiyohara H, Takemoto N, Zhao JF, Kawamura H, Komatsu Y, Cyong JC, Aburada M, Hosoya E (1992) Mitogenic and complement activating activities of the herbal components of Juzen-Taiho-To. Planta Medica 58: 166–170
Kiyohara H, Cyong JC, Yamada H (1989) Relationship between structure and activity of the “ramified” region in anti-complementary pectic polysaccharides from Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba,Part XII).Carbohydr Res 193: 201–214
Holst GJ, Clarke AE (1985) Quantification of arabinogalactan-protein plant extracts by single radial gel diffusion. Anal Biochem 148: 446–450
Kiyohara H, Cyong JC, Yamada H (1989) Relationship between structure and activity of an anti-complementary arabinogalactan from the roots of Angelica acutiloba Kitagawa. (Studies on polysaccharides from Angelica acutiloba, Part XI). Carbohydr Res 193: 193–200
Dey PM, Brinson K (1987) Plant cell-walls. Adv Carbohydr Chem Biochem 42: 265–382
Hirano M, Kiyohara H, Yamada H (1994) Existence of rhamnogalacturonan II-like region in bioactive pectins from medicinal herbs. Planta Medica 60: 450–454
Albersheim P, An J, Freshour G, Fuller MS, Guillen R, Ham KS, Hahn MG, Huang J, O’Neill M, Whitcombe A et al. (1994) Structure and function studies of plant cell wall polysaccharides. Biochem Soc Trans 22: 374–378
Tomoda M, Satoh N (1977) Plant mucilage XVII. Partial hydrolysis and a possible structure of paniculatan. Chem Pharm Bull 25: 2910–2916
Tomoda M, Shimizu N, Shimada K, Gonda R, Sakabe H (1984) Plant mucilages XXXIV. The location of O-acetyl groups and the structural features of plantagomucilage A, the mucous polysaccharide from the seeds of Plantago asiatica. Chem Pharm Bull 32: 2182–2186
Yamada H, Nagai T, Cyong JC, Otsuka Y (1991) Mode of complement activation by acidic heteroglycans from the leaves of Artemisia princeps PAMP. Chem Pharm Bull 39: 2077–2081
Yamada H, Nagai T, Cyong JC, Otsuka Y, Tomoda M, Shimizu N, Gonda R (1986) Relationship between chemical structure and activating potencies of complement by an acidic polysaccharide, Plantago-mucilage A, from the seed of Plantago asiatica. Carbohydr Res 156: 137–145
Blondin C, Fischer E, Boisson-Vidal C, Kazatchkine MD, Jozefonvicz J (1994) Inhibition of complement activation by natural sulfated polysaccharide (fucans) from brown seaweed. Molec Immunol 31: 247–253
Law S K, Lichtenberg NA, Levine RP (1979) Evidence for an ester linkage between the labile binding site of C3b and receptive surfaces. J Immunomol 123: 1388–1394
Pangburn MK (1989) Analysis of the mechanism of recognition in the complement alternative pathway using C3b-bound low molecular weight polysaccharides. J Immunomol 142: 2759–2765
Kiyohara H, Yamada H (1994) Characterisation of methyl-ester distributions in galacturonan regions of complement activating pectins from the roots of Angelica acutiloba Kitagawa. Carbohydr Polymers 25: 117–122
Yamada H, Hirano M, Kiyohara H (1991) Partial structure of an anti-ulcer pectic poly-saccharide from the roots of Bupleurum falcatum L.Carbohydr Res 219: 173–192
Zhang YW, Kiyohara H, Sakurai M, Yamada H (1996) Complement activating galactan chains in a pectic arabinogalactan (AGIIb-1) from the roots of Angelica acutiloba Kitagawa. Carbohydr Polymers 31: 149–156.
Tsumuraya Y, Mochizuki N, Hashimoto Y, Kovác P (1990) Purification of an exo-β(1→3)-galactanase of Irpex lacteus (Polyporus tulipiferae) and its action on arabinogalactan-proteins. J Biol Chem 265: 7207–7215
Kiyohara H, Zhang YW, Yamada H (1997) Effect of exo β-D-(1→3) galactanase digestion on complement activating activity of neutral arabinogalactan unit in a pectic arabinogalactan from roots of Angelica acutiloba Kitagawa. Carbohydr Polymers 32: 249–253
Kiyohara H, Takemoto N, Zhao JF, Kawamura H, Yamada H (1996) Pectic polysaccharide from roots of Glycyrrhiza uralensis: Possible contribution of neutral oligosaccharide in the galacturonase-resistant region to anti-complementary and mitogenic activities. In: Visser J, Voragen AGJ (eds): Pectin and pectinase. Progress in biotechnology, Vol. 4. Elsevier, Amsterdam, 673–678
Kiyohara H, Takemoto N, Zhao JF, Kawamura H, Yamada H (1996) Pectic polysaccharide from roots of Glycyrrhiza uralensis: Possible contribution of neutral oligosaccharide in the galacturonase-resistant region to anti-complementary and mitogenic activities. Planta Medica 62: 14–19
Rosenberg RD (1977) Chemistry of the hemostatic mechanism and its relationship to the action of heparin. Fed Proc 36: 10–18
Maillet F, Kazatchkine MD, Glotz D, Fischer E, Row M (1983) Heparin prevents formation of the human C3 amplification convertase by inhibiting the binding site for B on C3b. Molec Immunol 20: 1401–1404
Maillet F, Petitou M, Choay J, Kazatchkine MD (1988) Structure-function relationships in the inhibitory effect of heparin on complement activation: In dependency of the anti-coagulant and anti-complementary sites on the heparin molecule. Molec Immunol 25: 917–923
Cooper PD, Carter M (1986) Anti-complementary action of polymorphic “solubility forms” of particulate inulin. Molec Immunol 23: 895–901
McDonald EJ (1946) The polyfructosans and difructose anhydrides. Adv Carbohydr Chem 2: 253–277
Honda S, Sugino H, Asano T, Kakinuma A (1986) Activation of the alternative pathway of complement by an anti-tumor (1→3)-β-D-glucan from Alcaligenes faecalis var. myxogenes IFO 13140 and its lower molecular weight and carboxymethylated derivatives. Immunopharmacol 11: 29–37
Yamada H (1994) Pectic polysaccharides from Chinese herbs: Structure and biological activity. Carbohydr Polymers 25: 269–276
Yamada H (1996) Contribution of pectins on health care. In: Visser J, Voragen AGJ (eds): Pectin and pectinase. Progress in biotechnology. Vol. 4, Elsevier, Amsterdam, 173–190
Wagner H (1990) Search for plant derived natural products with immunostimulatory activity (recent advances). Pure & App/ Chem 62: 1217–1222
Wagner H, Stuppner H, Schafer W, Zenk M (1988) Immunologically active polysaccharides of Echinacea purpurea cell cultures. Phytochem 27: 119–126
Stimple M, Proksch A, Wagner H, Lohmann-Matthes ML (1984) Macrophage activation and induction of macrophage cytotoxicity by purified polysaccharide fractions from the plant Echinacea purpurea. Infection and Immunity 46: 845–849
Luettg B, Steinmüller C, Gifford GE, Wagner H, Lohmann-Matthes ML (1989) Macrophage activation by the polysaccharide arabinogalactan isolated from plant cell cultures of Echinacea purpurea. J Natl Canc Inst 81: 669–675
Varljen J, Liptak A, Wagner H (1989) Structural analysis of a rhamnoarabinogalactan and arabinogalactans with immuno-stimulating activity from Calendula o f ficinalis. Phytochem 28: 2379–2383
Yamada H, Komiyama K, Kiyohara H, Cyong JC, Hirakawa Y, Otsuka Y (1990) Structural characterization and antitumor activity of a pectic polysaccharide from the roots of Angelica acutiloba. (Studies on polysaccharides form Angelica acutiloba, Part XIII). Planta Medica 56: 182–186
Matsumoto T, Tanaka M, Yamada H, Cyong JC (1990) A new photometric microassay for quantitation of macrophage Fc receptor function: in vitro enzyme-containing immune complex clearance (EIC) assay. J Immunol Methods 129: 283–290
Matsumoto T, Cyong JC, Kiyohara H, Matsui H, Abe A, Hirano M, Danbara H, Yamada H (1993) The pectic polysaccharides from Bupleurum falcatum L. enhances immune-complexes binding to peritoneal macrophages through Fc receptor expression. Int J Immunopharmacol 15: 683–693
Matsumoto T, Yamada H (1996) The pectic polysaccharide from Bupleurum falcatum enhances immune complexes clearance in mice. Phytotherapy Res 10: 585–588
Matsumoto T, Yamada H (1995) Regulation of immune-complex binding of macrophages by pectic polysaccharide from Bupleurum falcatum L.: Pharmacological evidence for the requirement of intracellular calcium/calmodulin on Fc receptor up-regulation by bupleuran 2I1b. J Pharmacy Pharmacol 47: 152–156
Yamada H, Sun XB, Matsumoto T, Ra KS, Hirano M, Kiyohara H (1991) Purification of anti-ulcer polysaccharides from the roots of Bupleurum falcatum L.Planta Medica 57: 555–559.
Sun XB, Matsumoto T, Yamada H (1991) Effects of a polysaccharide fraction from the roots of Bupleurum falcatum L. on experimental gastric ulcer models in rats and mice. J Pharmacy Pharmacol 43: 699–704
Matsumoto T, Moriguchi R, Yamada H (1993) Role of polymorphonuclear leukocytes and oxygen-derived free radicals in the formation of gastric lesions induced by HCI/ethenol, and a possible mechanism of protection by anti-ulcer polysaccharide. J Pharmacy Pharmacol 45: 535–539
Hirano M, Kiyohara H, Matsumoto T, Yamada H (1994) Structural studies of endopolygalacturonase-resistant fragments in anti-ulcer pectin from the roots of Bupleurum falcatum L. Carbohydr Res 251: 145–162
Sakurai MH, Matsumoto T, Kiyohara H, Yamada H (1996) Detection and tissue distribution of anti-ulcer polysaccharides from Bupleurum falcatum L. by polyclonal antibody. Planta Medica 62: 341–346
Czop JK, Gurish MF, Kadish JL (1990) Production and isolation of rabbit anti-idiotypic antibodies directed against the human monocyte receptor for yeast ß-glucans. J Immunol 145: 995–1001
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer Basel AG
About this chapter
Cite this chapter
Yamada, H., Kiyohara, H. (1999). Complement-activating polysaccharides from medicinal herbs. In: Wagner, H. (eds) Immunomodulatory Agents from Plants. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8763-2_7
Download citation
DOI: https://doi.org/10.1007/978-3-0348-8763-2_7
Publisher Name: Birkhäuser, Basel
Print ISBN: 978-3-0348-9763-1
Online ISBN: 978-3-0348-8763-2
eBook Packages: Springer Book Archive