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Gardenia jasminoides extract and its constituent, genipin, inhibit activation of CD3/CD28 co-stimulated CD4+ T cells via ORAI1 channel

  • Kim, Hyun Jong (Channelopathy Research Center (CRC), Dongguk University College of Medicine) ;
  • Nam, Yu Ran (Channelopathy Research Center (CRC), Dongguk University College of Medicine) ;
  • Woo, JooHan (Channelopathy Research Center (CRC), Dongguk University College of Medicine) ;
  • Kim, Woo Kyung (Channelopathy Research Center (CRC), Dongguk University College of Medicine) ;
  • Nam, Joo Hyun (Channelopathy Research Center (CRC), Dongguk University College of Medicine)
  • Received : 2020.04.28
  • Accepted : 2020.06.05
  • Published : 2020.07.01

Abstract

Gardenia jasminoides (GJ) is a widely used herbal medicine with anti-inflammatory properties, but its effects on the ORAI1 channel, which is important in generating intracellular calcium signaling for T cell activation, remain unknown. In this study, we investigated whether 70% ethanolic GJ extract (GJEtOH) and its subsequent fractions inhibit ORAI1 and determined which constituents contributed to this effect. Whole-cell patch clamp analysis revealed that GJEtOH (64.7% ± 3.83% inhibition at 0.1 mg/ml) and all its fractions showed inhibitory effects on the ORAI1 channel. Among the GJ fractions, the hexane fraction (GJHEX, 66.8% ± 9.95% at 0.1 mg/ml) had the most potent inhibitory effects in hORAI1-hSTIM1 co-transfected HEK293T cells. Chemical constituent analysis revealed that the strong ORAI1 inhibitory effect of GJHEX was due to linoleic acid, and in other fractions, we found that genipin inhibited ORAI1. Genipin significantly inhibited IORAI1 and interleukin-2 production in CD3/CD28-stimulated Jurkat T lymphocytes by 35.9% ± 3.02% and 54.7% ± 1.32% at 30 μM, respectively. Furthermore, the same genipin concentration inhibited the proliferation of human primary CD4+ T lymphocytes stimulated with CD3/CD28 antibodies by 54.9% ± 8.22%, as evaluated by carboxyfluorescein succinimidyl ester assay. Our findings suggest that genipin may be one of the active components of GJ responsible for T cell suppression, which is partially mediated by activation of the ORAI1 channel. This study helps us understand the mechanisms of GJ in the treatment of inflammatory diseases.

Keywords

References

  1. Liu H, Chen YF, Li F, Zhang HY. Fructus Gardenia (Gardenia jasminoides J. Ellis) phytochemistry, pharmacology of cardiovascular, and safety with the perspective of new drugs development. J Asian Nat Prod Res. 2013;15:94-110. https://doi.org/10.1080/10286020.2012.723203
  2. Deng Y, Guan M, Xie X, Yang X, Xiang H, Li H, Zou L, Wei J, Wang D, Deng X. Geniposide inhibits airway inflammation and hyperresponsiveness in a mouse model of asthma. Int Immunopharmacol. 2013;17:561-567. https://doi.org/10.1016/j.intimp.2013.06.028
  3. Sung YY, Lee AY, Kim HK. The Gardenia jasminoides extract and its constituent, geniposide, elicit anti-allergic effects on atopic dermatitis by inhibiting histamine in vitro and in vivo. J Ethnopharmacol. 2014;156:33-40. https://doi.org/10.1016/j.jep.2014.07.060
  4. Koo HJ, Lim KH, Jung HJ, Park EH. Anti-inflammatory evaluation of gardenia extract, geniposide and genipin. J Ethnopharmacol. 2006;103:496-500. https://doi.org/10.1016/j.jep.2005.08.011
  5. Xiao W, Li S, Wang S, Ho CT. Chemistry and bioactivity of Gardenia jasminoides. J Food Drug Anal. 2017;25:43-61. https://doi.org/10.1016/j.jfda.2016.11.005
  6. Ko JW, Shin NR, Park SH, Cho YK, Kim JC, Seo CS, Shin IS. Genipin inhibits allergic responses in ovalbumin-induced asthmatic mice. Int Immunopharmacol. 2017;53:49-55. https://doi.org/10.1016/j.intimp.2017.10.010
  7. Nam JH, Kim WK. The role of TRP channels in allergic inflammation and its clinical relevance. Curr Med Chem. 2020;27:1446-1468. https://doi.org/10.2174/0929867326666181126113015
  8. Litosch I. Decoding $G{\alpha}q$ signaling. Life Sci. 2016;152:99-106. https://doi.org/10.1016/j.lfs.2016.03.037
  9. Woo JS, Srikanth S, Gwack Y. Modulation of Orai1 and STIM1 by cellular factors. In: Kozak JA, Putney JW Jr, editors. Calcium entry channels in non-excitable cells. Boca Raton (FL): CRC Press; 2018. p.73-92.
  10. Feske S, Wulff H, Skolnik EY. Ion channels in innate and adaptive immunity. Annu Rev Immunol. 2015;33:291-353. https://doi.org/10.1146/annurev-immunol-032414-112212
  11. Kim HJ, Nam YR, Kim EJ, Nam JH, Kim WK. Spirodela polyrhiza and its chemical constituent vitexin exert anti-allergic effect via ORAI1 channel inhibition. Am J Chin Med. 2018;46:1243-1261. https://doi.org/10.1142/S0192415X18500659
  12. Kim HJ, Woo J, Nam YR, Nam JH, Kim WK. Flos Magnoliae and its constituent linoleic acid suppress T lymphocyte activation via store-operated calcium entry. Am J Chin Med. 2019;47:1627-1641. https://doi.org/10.1142/S0192415X19500836
  13. Lee S, Youn K, Jun M. Major compounds of red ginseng oil attenuate $A{\beta}25$-35-induced neuronal apoptosis and inflammation by modulating MAPK/NF-${\kappa}B$ pathway. Food Funct. 2018;9:4122-4134. https://doi.org/10.1039/C8FO00795K
  14. Gabay O, Sanchez C, Salvat C, Chevy F, Breton M, Nourissat G, Wolf C, Jacques C, Berenbaum F. Stigmasterol: a phytosterol with potential anti-osteoarthritic properties. Osteoarthritis Cartilage. 2010;18:106-116. https://doi.org/10.1016/j.joca.2009.08.019
  15. Trickett A, Kwan YL. T cell stimulation and expansion using anti-CD3/CD28 beads. J Immunol Methods. 2003;275:251-255. https://doi.org/10.1016/S0022-1759(03)00010-3
  16. Park SH, An JE, Jang S, Kim JY, Lee JW, Kim HK. Gardenia jasminoides extract without crocin improved atopic dermatitis-like skin lesions via suppression of Th2-related cytokines in Dfe-induced NC/ Nga mice. J Ethnopharmacol. 2019;241:112015. https://doi.org/10.1016/j.jep.2019.112015
  17. Sung YY, Kim HK. Crocin ameliorates atopic dermatitis symptoms by down regulation of Th2 response via blocking of NF-${\kappa}B$/STAT6 signaling pathways in mice. Nutrients. 2018;10:1625. https://doi.org/10.3390/nu10111625
  18. Srikanth S, Woo JS, Sun Z, Gwack Y. Immunological disorders: regulation of $Ca^{2+}$ signaling in T lymphocytes. Adv Exp Med Biol. 2017;993:397-424. https://doi.org/10.1007/978-3-319-57732-6_21
  19. Holowka D, Wilkes M, Stefan C, Baird B. Roles for $Ca^{2+}$ mobilization and its regulation in mast cell functions: recent progress. Biochem Soc Trans. 2016;44:505-509. https://doi.org/10.1042/BST20150273
  20. Shanmugam MK, Shen H, Tang FR, Arfuso F, Rajesh M, Wang L, Kumar AP, Bian J, Goh BC, Bishayee A, Sethi G. Potential role of genipin in cancer therapy. Pharmacol Res. 2018;133:195-200. https://doi.org/10.1016/j.phrs.2018.05.007
  21. Habtemariam S, Lentini G. Plant-derived anticancer agents: lessons from the pharmacology of geniposide and its aglycone, genipin. Biomedicines . 2018;6:39. https://doi.org/10.3390/biomedicines6020039
  22. Zhang Z, Wang X, Ma C, Li Z, Chen H, Zhang Z, Li T. Genipin protects rats against lipopolysaccharide-induced acute lung injury by reinforcing autophagy. Int Immunopharmacol. 2019;72:21-30. https://doi.org/10.1016/j.intimp.2019.03.052
  23. Yu SX, Du CT, Chen W, Lei QQ, Li N, Qi S, Zhang XJ, Hu GQ, Deng XM, Han WY, Yang YJ. Genipin inhibits NLRP3 and NLRC4 inflammasome activation via autophagy suppression. Sci Rep. 2015;5:17935. https://doi.org/10.1038/srep17935
  24. Kim JS, Kim SJ, Lee SM. Genipin attenuates sepsis-induced immunosuppression through inhibition of T lymphocyte apoptosis. Int Immunopharmacol. 2015;27:15-23. https://doi.org/10.1016/j.intimp.2015.04.034
  25. Nam KN, Choi YS, Jung HJ, Park GH, Park JM, Moon SK, Cho KH, Kang C, Kang I, Oh MS, Lee EH. Genipin inhibits the inflammatory response of rat brain microglial cells. Int Immunopharmacol. 2010;10:493-499. https://doi.org/10.1016/j.intimp.2010.01.011