Extract of Reishi Polysaccharides Induces Cytokine Expression via TLR4-Modulated Protein Kinase Signaling Pathways1

We have demonstrated that an extract of Ganoderma lucidum (Reishi or Ling-Zhi) polysaccharides (EORP) exerts immunomodulating activities by stimulating the expression of inflammatory cytokines from mouse spleen cells. Interestingly, via responding to LPS in genetic variation of murine macrophage HeNC2 and GG2EE cell lines, and using TLR4 Ab blockage in human blood-derived monocytic macrophages, we have found that the TLR4, but not complement receptor type 3, is a putative receptor of EORP, mediating the consequent immunomodulating events associated with IL-1 gene expression. Based on our studies of reactive oxygen species production, polymyxin B inhibition, and protein tyrosine kinase (PTK) activity, we ruled out the possibility of LPS contamination in EORP. We have found that EORP differentially modulates the protein kinase (PK)-mediated signal transduction pathways associated with inflammatory cytokine IL-1. In human macrophages and murine macrophage J774A.1 cells, EORP was found to up-regulate IL-1 secretion and pro-IL-1 (precursor of IL-1) as well as IL-1-converting enzyme expression. Specifically, EORP rapidly stimulates PTK-mediated phosphorylation, followed by induction of PKs and activation of MAPKs: ERK, JNK, and p38. Using PK inhibitors in the kinase activity assays, Western blot analyses and IL-1 ELISA, we have extensively examined and dissected the role of individual PK in the regulation of pro-IL-1/IL-1. Our findings establish that EORP-mediated signaling pathways are involved in the pro-IL-1/IL-1 regulation: PTK/protein kinase C/MEK1/ERK and PTK/Rac1/p21-activated kinase/p38.

[1]  E. Lien Fungal metabolites and Chinese herbal medicine as immunostimulants. , 1990, Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques.

[2]  D. Melican,et al.  Enhanced clearance of a multiple antibiotic resistant Staphylococcus aureus in rats treated with PGG-glucan is associated with increased leukocyte counts and increased neutrophil oxidative burst activity. , 1998, International journal of immunopharmacology.

[3]  Kay-Hooi Khoo,et al.  Studies on the immuno-modulating and antitumor activities of Ganoderma lucidum (Reishi) polysaccharides: functional and proteomic analyses of a fucose-containing glycoprotein fraction responsible for the activities. , 2002, Bioorganic & medicinal chemistry.

[4]  Hsien-Yeh Hsu,et al.  Lipopolysaccharide-mediated Reactive Oxygen Species and Signal Transduction in the Regulation of Interleukin-1 Gene Expression* , 2002, The Journal of Biological Chemistry.

[5]  M. Quinn,et al.  Modulation of Endotoxin- and Enterotoxin-Induced Cytokine Release by In Vivo Treatment with β-(1,6)-Branched β-(1,3)-Glucan , 1999, Infection and Immunity.

[6]  Y. Adachi,et al.  Nitric Oxide Synthesis in Murine Peritoneal Macrophages by Fungal β-Glucans , 1997 .

[7]  T. Miyazaki,et al.  Studies on fungal polysaccharides. XXVII. Structural examination of a water-soluble, antitumor polysaccharide of Ganoderma lucidum. , 1981, Chemical & pharmaceutical bulletin.

[8]  P. Lachmann,et al.  Membrane complement receptor type three (CR3) has lectin-like properties analogous to bovine conglutinin as functions as a receptor for zymosan and rabbit erythrocytes as well as a receptor for iC3b. , 1985, Journal of immunology.

[9]  Philip R. Cohen,et al.  PD 098059 Is a Specific Inhibitor of the Activation of Mitogen-activated Protein Kinase Kinase in Vitro and in Vivo(*) , 1995, The Journal of Biological Chemistry.

[10]  S. Chiu,et al.  Ligands of Macrophage Scavenger Receptor Induce Cytokine Expression via Differential Modulation of Protein Kinase Signaling Pathways* , 2001, The Journal of Biological Chemistry.

[11]  K. Kataoka,et al.  Activation of Macrophages by Linear (1→3)-β-d-Glucans , 2002, The Journal of Biological Chemistry.

[12]  J. Bennett,et al.  Beta 1,4-oligoglucosides inhibit the binding of Aspergillus fumigatus conidia to human monocytes. , 1991, The Journal of infectious diseases.

[13]  Yoshinori Nagai,et al.  MD-2, a Molecule that Confers Lipopolysaccharide Responsiveness on Toll-like Receptor 4 , 1999, The Journal of experimental medicine.

[14]  L. Larivière,et al.  Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4) , 1999, The Journal of experimental medicine.

[15]  T. Mizuno,et al.  Antitumor active polysaccharides from the Chinese mushroom Songshan lingzhi, the fruiting body of Ganoderma tsugae. , 1993, Bioscience, biotechnology, and biochemistry.

[16]  V. Vetvicka,et al.  Analysis of the sugar specificity and molecular location of the beta-glucan-binding lectin site of complement receptor type 3 (CD11b/CD18). , 1996, Journal of immunology.

[17]  S. Akira,et al.  Cutting edge: Toll-like receptor 4 (TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. , 1999, Journal of immunology.

[18]  T. Okada,et al.  Blockage of chemotactic peptide-induced stimulation of neutrophils by wortmannin as a result of selective inhibition of phosphatidylinositol 3-kinase. , 1994, The Journal of biological chemistry.

[19]  Y. Sone,et al.  Structures and Antitumor Activities of the Polysaccharides Isolated from Fruiting Body and the Growing Culture of Mycelium of Ganoderma lucidum , 1985 .

[20]  C. Hall,et al.  Molecular Cloning of a New Member of the p21-Cdc42/Rac-activated Kinase (PAK) Family (*) , 1995, The Journal of Biological Chemistry.

[21]  Chi-Tang Ho,et al.  Food Phytochemicals for Cancer Prevention II: Teas, Spices, and Herbs , 1994 .

[22]  P. Ricciardi-Castagnoli,et al.  Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. , 1998, Science.

[23]  Siamon Gordon,et al.  Dectin-1 Is A Major β-Glucan Receptor On Macrophages , 2002, The Journal of experimental medicine.

[24]  M. J. Barratt,et al.  p38/RK is essential for stress-induced nuclear responses: JNK/SAPKs and c-Jun/ATF-2 phosphorylation are insufficient , 1996, Current Biology.

[25]  J. Standing,et al.  Isolated Pneumocystis carinii Cell Wall Glucan Provokes Lower Respiratory Tract Inflammatory Responses1 , 2000, The Journal of Immunology.

[26]  S. Cook,et al.  The Selective Protein Kinase C Inhibitor, Ro-31-8220, Inhibits Mitogen-activated Protein Kinase Phosphatase-1 (MKP-1) Expression, Induces c-Jun Expression, and Activates Jun N-terminal Kinase* , 1996, The Journal of Biological Chemistry.

[27]  J. Bennett,et al.  Lectin-like attachment sites on murine pulmonary alveolar macrophages bind Aspergillus fumigatus conidia. , 1988, The Journal of infectious diseases.

[28]  H. S. Warren,et al.  Toll-like receptors. , 2005, Critical care medicine.

[29]  Xiao-yu Li,et al.  Structural features of immunologically active polysaccharides from Ganoderma lucidum. , 2002, Phytochemistry.

[30]  M. Shiao,et al.  Natural Products and Biological Activities of the Chinese Medicinal Fungus Ganoderma lucidum , 1994 .

[31]  V. Vetvicka,et al.  Soluble beta-glucan polysaccharide binding to the lectin site of neutrophil or natural killer cell complement receptor type 3 (CD11b/CD18) generates a primed state of the receptor capable of mediating cytotoxicity of iC3b-opsonized target cells. , 1996, The Journal of clinical investigation.

[32]  C. Ho,et al.  The anti‐tumor effect of Ganoderma Lucidum is mediated by cytokines released from activated macrophages and T lymphocytes , 1997, International journal of cancer.

[33]  Yau-Huei Wei,et al.  Antitumor Effects of Ganoderma Lucidum , 1995 .

[34]  C. Marshall,et al.  Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells , 1994, Cell.

[35]  David W. Anderson,et al.  SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[36]  J. J. Crowley,et al.  PGG-Glucan, a soluble β-(1,3)-glucan, enhances the oxidative burst response, microbicidal activity, and activates an NF-κB-like factor in human PMN: Evidence for a glycosphingolipid β-(1,3)-glucan receptor , 1999 .

[37]  A. Wettstein Fortschritte der Arzneimittelforschung , 1960, Experientia.

[38]  T. Hartung,et al.  Induction of Cross-Tolerance by Lipopolysaccharide and Highly Purified Lipoteichoic Acid Via Different Toll-Like Receptors Independent of Paracrine Mediators1 , 2001, The Journal of Immunology.

[39]  N. Ip,et al.  Ganoderma extract activates MAP kinases and induces the neuronal differentiation of rat pheochromocytoma PC12 cells , 2000, FEBS letters.

[40]  Jiahuai Han,et al.  Rho Family GTPases Regulate p38 Mitogen-activated Protein Kinase through the Downstream Mediator Pak1 (*) , 1995, The Journal of Biological Chemistry.

[41]  A. Aderem,et al.  Toll-like receptors in the induction of the innate immune response , 2000, Nature.

[42]  S. Akira,et al.  Toll-like receptors: critical proteins linking innate and acquired immunity , 2001, Nature Immunology.

[43]  Y. Twu,et al.  Tumor Necrosis Factor-α-mediated Protein Kinases in Regulation of Scavenger Receptor and Foam Cell Formation on Macrophage* , 2000, The Journal of Biological Chemistry.