Acknowledgement
This study was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean Government (MEST) (NRF-2020R1I1A1A01064838). Prof. JS Ryu Hanyang University Colleage of Medicine in acknowledged for kind alonation of the T016 strain of T. vaginalis.
References
- Ryu JS, Min DY. Trichomonas vaginalis and trichomoniasis in the Republic of Korea. Korean J Parasitol 2006;44(2):101-116. https://doi.org/10.3347/kjp.2006.44.2.101
- Han IH, Kim JH, Ryu JS. Inflammatory response to Trichomonas vaginalis in the pathogenesis of prostatitis and benign prostatic hyperplasia. Parasites Hosts Dis 2023;61(1):2-14. https://doi.org/10.3347/PHD.22160
- Mercer F, Johnson PJ. Trichomonas vaginalis: pathogenesis, symbiont interactions, and host cell immune responses. Trends Parasitol 2018;34(8):683-693. https://doi.org/10.1016/j.pt.2018.05.006
- Szempruch AJ, Dennison L, Kieft R, Harrington JM, Hajduk SL. Sending a message: extracellular vesicles of pathogenic protozoan parasites. Nat Rev Microbiol 2016;14(11):669-675. https://doi.org/10.1038/nrmicro.2016.110
- Preta G, Cronin JG, Sheldon IM. Dynasore - not just a dynamin inhibitor. Cell Commun Signal 2015;13:24. https://doi.org/10.1186/s12964-015-0102-1
- Kim HS, Kawakami Y, Kasakura K, Kawakami T. Recent advances in mast cell activation and regulation. F1000Res 2020;9:F1000 Faculty Rev-196. https://doi.org/10.12688/f1000research.22037.1
- Shaio MF, Lin PR, Lee CS, Hou SC, Tang P, et al. A novel neutrophil-activating factor released by Trichomonas vaginalis. Infect Immun 1992;60(11):4475-4482. https://doi.org/10.1128/iai.60.11.4475-4482.1992
- Nam YH, Min D, Kim HP, Song KJ, Kim KA, et al. Leukotriene B4 receptor BLT-mediated phosphorylation of NF-κB and CREB is involved in IL-8 production in human mast cells induced by Trichomonas vaginalis-derived secretory products. Microbes Infect 2011;13(14-15):1211-1220. https://doi.org/10.1016/j.micinf.2011.07.006
- Min A, Lee YA, Kim KA, Shin MH. BLT1-mediated O-GlcNAcylation is required for NOX2-dependent migration, exocytotic degranulation and IL-8 release of human mast cell induced by Trichomonas vaginalis-secreted LTB(4). Microbes Infect 2018;20(6):376-384. https://doi.org/10.1016/j.micinf.2018.05.005
- Kobayashi TK, Fujimoto T, Okamoto H, Yuasa M, Sawaragi I. Association of mast cells with vaginal trichomoniasis in endocervical smears. Acta Cytol 1983;27(2):133-137.
- Narantsogt G, Min A, Nam YH, Lee YA, Kim KA, et al. Activation of MAPK is required for ROS generation and exocytosis in HMC-1 cells induced by Trichomonas vaginalis-derived secretory products. Korean J Parasitol 2015;53(5):597-603. https://doi.org/10.3347/kjp.2015.53.5.597
- Cardamone C, Parente R, Feo GD, Triggiani M. Mast cells as effector cells of innate immunity and regulators of adaptive immunity. Immunol Lett 2016;178:10-14. https://doi.org/10.1016/j.imlet.2016.07.003
- Calebiro D, Godbole A. Internalization of G-protein-coupled receptors: implication in receptor function, physiology and diseases. Best Pract Res Clin Endocrinol Metab 2018;32(2):83-91. https://doi.org/10.1016/j.beem.2018.01.004
- Ferguson SM, De Camilli P. Dynamin, a membrane-remodel-ling GTPase. Nat Rev Mol Cell Biol 2012;13(2):75-88. https://doi.org/10.1038/nrm3266
- Praefcke GJ, McMahon HT. The dynamin superfamily: universal membrane tubulation and fission molecules? Nat Rev Mol Cell Biol 2004;5(2):133-147. https://doi.org/10.1038/nrm1313
- Kim YN, Bertics PJ. The endocytosis-linked protein dynamin associates with caveolin-1 and is tyrosine phosphorylated in response to the activation of a noninternalizing epidermal growth factor receptor mutant. Endocrinology 2002;143(5):1726-1731. https://doi.org/10.1210/endo.143.5.8814
- van Dam EM, Stoorvogel W. Dynamin-dependent transferrin receptor recycling by endosome-derived clathrin-coated vesicles. Mol Biol Cell 2002;13(1):169-182. https://doi.org/10.1091/mbc.01-07-0380
- Ahn S, Maudsley S, Luttrell LM, Lefkowitz RJ, Daaka Y. Srcmediated tyrosine phosphorylation of dynamin is required for beta2-adrenergic receptor internalization and mitogen-activated protein kinase signaling. J Biol Chem 1999;274(3):1185-1188. https://doi.org/10.1074/jbc.274.3.1185
- Lajoie P, Nabi IR. Lipid rafts, caveolae, and their endocytosis. Int Rev Cell Mol Biol 2010;282:135-163. https://doi.org/10.1016/S1937-6448(10)82003-9
- Silveira E Souza AM, Mazucato VM, Jamur MC, Oliver C. Lipid rafts in mast cell biology. J Lipids 2011;2011:752906. https://doi.org/10.1155/2011/752906
- Varshney P, Yadav V, Saini N. Lipid rafts in immune signalling: current progress and future perspective. Immunology 2016; 149(1):13-24. https://doi.org/10.1111/imm.12617
- Villar VA, Cuevas S, Zheng X, Jose PA. Localization and signaling of GPCRs in lipid rafts. Methods Cell Biol 2016;132:3-23. https://doi.org/10.1016/bs.mcb.2015.11.008
- Serezani CH, Aronoff DM, Sitrin RG, Peters-Golden M. FcgammaRI ligation leads to a complex with BLT1 in lipid rafts that enhances rat lung macrophage antimicrobial functions. Blood 2009;114(15):3316-3324. https://doi.org/10.1182/blood2009-01-199919
- Hermanns HM, Wohlfahrt J, Mais C, Hergovits S, Jahn D, et al. Endocytosis of pro-inflammatory cytokine receptors and its relevance for signal transduction. Biol Chem 2016;397(8):695-708. https://doi.org/10.1515/hsz-2015-0277
- Zhao Q, Qian Y, Li R, Tan B, Han H, et al. Norcantharidin facilitates LPS-mediated immune responses by up-regulation of AKT/NF-kappaB signaling in macrophages. PLoS One 2012;7(9):e44956. https://doi.org/10.1371/journal.pone.0044956
- Pietila TE, Latvala S, Osterlund P, Julkunen I. Inhibition of dynamin-dependent endocytosis interferes with type III IFN expression in bacteria-infected human monocyte-derived DCs. J Leukoc Biol 2010;88(4):665-674. https://doi.org/10.1189/jlb.1009651
- Miller FJ Jr, Chu X, Stanic B, Tian X, Sharma RV, et al. A differential role for endocytosis in receptor-mediated activation of Nox1. Antioxid Redox Signal 2010;12(5):583-593. https://doi.org/10.1089/ars.2009.2857
- Willinger T, Staron M, Ferguson SM, De Camilli P, Flavell RA. Dynamin 2-dependent endocytosis sustains T-cell receptor signaling and drives metabolic reprogramming in T lymphocytes. Proc Natl Acad Sci U S A 2015;112(14):4423-4428. https://doi.org/10.1073/pnas.1504279112
- Subramanian BC, Majumdar R, Parent CA. The role of the LTB(4)-BLT1 axis in chemotactic gradient sensing and directed leukocyte migration. Semin Immunol 2017;33:16-29. https://doi.org/10.1016/j.smim.2017.07.002
- Min A, Lee YA, Kim KA, El-Benna J, Shin MH. SNAP23-dependent surface translocation of leukotriene B4 (LTB4) receptor 1 is essential for NOX2-mediated exocytotic degranulation in human mast cells induced by Trichomonas vaginalis-secreted LTB4. Infect Immun 2016;85(1):e00526-16. https://doi.org/10.1128/IAI.00526-16