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Induction of Dectin-1 Expression and Intracellular Signal Transduction by β-Glucan of Ganoderma lucidum

불로초의 β-Glucan에 의한 Dectin-1 발현 유도와 세포 내 신호전달

  • Ryu, Han Wook (Department of Life Sciences, University of Seoul) ;
  • Kim, Ha Won (Department of Life Sciences, University of Seoul)
  • 유한욱 (서울시립대학교 생명과학과) ;
  • 김하원 (서울시립대학교 생명과학과)
  • Received : 2018.03.05
  • Accepted : 2018.05.15
  • Published : 2018.06.01

Abstract

Fungal ${\beta}$-glucan, known to have immunostimulatory and antitumor activities, can be recognized by host immune cells as one of the pathogen-associated molecular patterns (PAMPs). Although there are several reports on the diverse immunostimulatory activities of ${\beta}$-glucan, little is known about the intracellular signal transduction of ${\beta}$-glucan. Stimulation of RAW264.7 macrophage cells with ${\beta}$-glucan from Ganoderma lucidum induced the expressions of dectin-1, toll-like receptor 2 (TLR2), TLR4, and TLR6 at the transcription stage. Treatment with ${\beta}$-glucan also induced inflammatory mediators such as macrophage inflammatory proteins (MIP)-$1{\alpha}$, MIP-$1{\beta}$, MIP-$1{\gamma}$, interleukin (IL)-$1{\beta}$, and tumor necrosis factor (TNF)-${\alpha}$. Treatment of the cells with polymyxin B, an inhibitor of lipopolysaccharides (LPS), blocked the induction of inflammatory mediators in LPS- or ${\beta}$-glucan-stimulated systems. Pretreatment of the cells in our cell culture system with LY294002, a phosphoinositide 3-kinase (PI3K) inhibitor, or U0126, a mitogen-activated protein kinase/extracellular-signal-regulated kinase (MAPK/ERK) kinase (MEK)1/MEK2 inhibitor, led to a reduction in the induction of inflammatory mediators in a concentration-dependent manner. These results show that stimulation of the macrophage cells by ${\beta}$-glucan induced the expressions of both dectin-1 and TLRs. We also found that the PI3K/Akt and MEK pathways were involved in the induction of inflammatory mediators in macrophage cells during intracellular signal transduction of ${\beta}$-glucan.

진균류 유래의 ${\beta}$-glucan은 pathogen-associated molecular patterns의 일종이기도 하며 면역촉진과 항암작용을 나타냄이 알려져 있지만 세포 내 신호전달에 관해서는 알려진 바가 많지 않다. 대식세포주인 RAW264.7 세포에 불로초에서 추출한 ${\beta}$-glucan을 처리하였을 때 세포막에서는 덱틴-1, toll-like receptor 2, 4, 6의 발현이 증가되었으며, 세포 내에서는 macrophage inflammatory protein (MIP)-1a, MIP-$1{\beta}$, MIP-$1{\gamma}$, IL-$1{\beta}$ 그리고 tumor necrosis factor (TNF)-${\alpha}$의 발현이 증가되었다. 또한 대식세포주에 불로초의 ${\beta}$-glucan과 PI3K 또는 MEK1/MEK2 억제제를 각각 처리하였을 때에 세포 내의 MIP-1a, MIP-$1{\beta}$, MIP-$1{\gamma}$, interleukin-$1{\beta}$, TNF-${\alpha}$의 발현이 감소되었다. 따라서 불로초의 ${\beta}$-glucan은 대식세포에서 MyD88의 경로인 PI3K/Akt를 경유할 뿐만 아니라 MEK 경로를 활성화시킴으로써 다양한 면역조절작용이 가능한 것으로 여겨진다.

Keywords

References

  1. Fraiture M, Brunner F. Killing two birds with one stone: trans-kingdom suppression of PAMP/MAMP-induced immunity by T3E from enteropathogenic bacteria. Front Microbiol 2014;5:320.
  2. Chow J, Franz KM, Kagan JC. PRRs are watching you: localization of innate sensing and signaling regulators. Virology 2015;479-480:104-9. https://doi.org/10.1016/j.virol.2015.02.051
  3. McKenna K, Beignon AS, Bhardwaj N. Plasmacytoid dendritic cells: linking innate and adaptive immunity. J Virol 2005;79:17-27. https://doi.org/10.1128/JVI.79.1.17-27.2005
  4. Schnaar RL. Glycobiology simplified: diverse roles of glycan recognition in inflammation. J Leukoc Biol 2016;99:825-38. https://doi.org/10.1189/jlb.3RI0116-021R
  5. Watzlawick R, Kenngott EE, Liu FD, Schwab JM, Hamann A. Anti-inflammatory effects of IL-27 in zymosan-induced peritonitis: inhibition of neutrophil recruitment partially explained by impaired mobilization from bone marrow and reduced chemokine levels. PLoS One 2015;10:e0137651. https://doi.org/10.1371/journal.pone.0137651
  6. Muller A, Rice PJ, Ensley HE, Coogan PS, Kalbfleish JH, Kelley JL, Love EJ, Portera CA, Ha T, Browder IW, et al. Receptor binding and internalization of a water-soluble (1->3)-beta-D-glucan biologic response modifier in two monocyte/macrophage cell lines. J Immunol 1996;156:3418-25.
  7. Brown GD, Gordon S. Fungal beta-glucans and mammalian immunity. Immunity 2003;19:311-5. https://doi.org/10.1016/S1074-7613(03)00233-4
  8. Varki A, Cummings RD, Esko JD, Stanley P, Hart GW, Aebi M, Darvill AG, Kinoshita T, Packer NH, Prestegard JH, et al. Essentials of glycobiology. 3rd ed. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 2017.
  9. Figdor CG, van Kooyk Y, Adema GJ. C-type lectin receptors on dendritic cells and Langerhans cells. Nat Rev Immunol 2002;2:77-84. https://doi.org/10.1038/nri723
  10. Cambi A, Figdor CG. Dual function of C-type lectin-like receptors in the immune system. Curr Opin Cell Biol 2003;15:539-46. https://doi.org/10.1016/j.ceb.2003.08.004
  11. Rogers NC, Slack EC, Edwards AD, Nolte MA, Schulz O, Schweighoffer E, Williams DL, Gordon S, Tybulewicz VL, Brown GD, et al. Syk-dependent cytokine induction by Dectin-1 reveals a novel pattern recognition pathway for C type lectins. Immunity 2005;22:507-17. https://doi.org/10.1016/j.immuni.2005.03.004
  12. Underhill DM, Rossnagle E, Lowell CA, Simmons RM. Dectin-1 activates Syk tyrosine kinase in a dynamic subset of macrophages for reactive oxygen production. Blood 2005;106:2543-50. https://doi.org/10.1182/blood-2005-03-1239
  13. Gantner BN, Simmons RM, Canavera SJ, Akira S, Underhill DM. Collaborative induction of inflammatory responses by dectin-1 and toll-like receptor 2. J Exp Med 2003;197:1107-17. https://doi.org/10.1084/jem.20021787
  14. Lee JY, Ye J, Gao Z, Youn HS, Lee WH, Zhao L, Sizemore N, Hwang DH. Reciprocal modulation of Toll-like receptor-4 signaling pathways involving MyD88 and phosphatidylinositol 3-kinase/AKT by saturated and polyunsaturated fatty acids. J Biol Chem 2003;278:37041-51. https://doi.org/10.1074/jbc.M305213200
  15. Herre J, Marshall AS, Caron E, Edwards AD, Williams DL, Schweighoffer E, Tybulewicz V, Reis e Sousa C, Gordon S, Brown GD. Dectin-1 uses novel mechanisms for yeast phagocytosis in macrophages. Blood 2004;104:4038-45. https://doi.org/10.1182/blood-2004-03-1140
  16. Loures FV, Araújo EF, Feriotti C, Bazan SB, Calich VL. TLR-4 cooperates with Dectin-1 and mannose receptor to expand Th17 and Tc17 cells induced by Paracoccidioides brasiliensis stimulated dendritic cells. Front Microbiol 2015;6:261.
  17. Underhill DM, Ozinsky A. Phagocytosis of microbes: complexity in action. Annu Rev Immunol 2002;20:825-52. https://doi.org/10.1146/annurev.immunol.20.103001.114744
  18. Roeder A, Kirschning CJ, Rupec RA, Schaller M, Weindl G, Korting HC. Toll-like receptors as key mediators in innate antifungal immunity. Med Mycol 2004;42:485-98. https://doi.org/10.1080/13693780400011112
  19. Gensel JC, Wang Y, Guan Z, Beckwith KA, Braun KJ, Wei P, McTigue DM, Popovich PG. Toll-like receptors and Dectin-1, a C-type lectin receptor, trigger divergent functions in CNS macrophages. J Neurosci 2015;35:9966-76. https://doi.org/10.1523/JNEUROSCI.0337-15.2015
  20. Underhill DM. Macrophage recognition of zymosan particles. J Endotoxin Res 2003;9:176-80. https://doi.org/10.1177/09680519030090030601
  21. Heinsbroek SE, Taylor PR, Rosas M, Willment JA, Williams DL, Gordon S, Brown GD. Expression of functionally different dectin-1 isoforms by murine macrophages. J Immunol 2006;176:5513-8. https://doi.org/10.4049/jimmunol.176.9.5513
  22. Tzianabos AO. Polysaccharide immunomodulators as therapeutic agents: structural aspects and biologic function. Clin Microbiol Rev 2000;13:523-33. https://doi.org/10.1128/CMR.13.4.523-533.2000
  23. Masuoka J. Surface glycans of Candida albicans and other pathogenic fungi: physiological roles, clinical uses, and experimental challenges. Clin Microbiol Rev 2004;17:281-310. https://doi.org/10.1128/CMR.17.2.281-310.2004
  24. Alaei S, Larcher C, Ebenbichler C, Prodinger WM, Janatova J, Dierich MP. Isolation and biochemical characterization of the iC3b receptor of Candida albicans. Infect Immun 1993;61:1395-9.
  25. Ramos CD, Canetti C, Souto JT, Silva JS, Hogaboam CM, Ferreira SH, Cunha FQ. MIP-1alpha[CCL3] acting on the CCR1 receptor mediates neutrophil migration in immune inflammation via sequential release of TNF-alpha and LTB4. J Leukoc Biol 2005;78:167-77. https://doi.org/10.1189/jlb.0404237
  26. Chen HS, Tsai YF, Lin S, Lin CC, Khoo KH, Lin CH, Wong CH. Studies on the immuno-modulating and anti-tumor activities of Ganoderma lucidum (Reishi) polysaccharides. Bioorg Med Chem 2004;12:5595-601. https://doi.org/10.1016/j.bmc.2004.08.003