Acknowledgement
We thank the Metabolomics Core Facility at the Convergence medicine research center (CREDIT), Asan Medical Center for support and instrumentation. This research was supported by the Basic Research Laboratory Program (BRL) and the Basic Science Research Program of the Korean National Research Foundation funded by the Korean Ministry of Science, ICT, and Future Planning (NRF-2020R1A4A1016142 and NRF-2019R1A2C1005523).
References
- Arrighi, J.-F., Rebsamen, M., Rousset, F., Kindler, V. and Hauser, C. (2001) A critical role for p38 mitogen-activated protein kinase in the maturation of human blood-derived dendritic cells induced by lipopolysaccharide, TNF-α, and contact sensitizers. J. Immunol. 166, 3837-3845. https://doi.org/10.4049/jimmunol.166.6.3837
- Azzolina, A., Guarneri, P. and Lampiasi, N. (2002) Involvement of p38 and JNK MAPKs pathways in substance P-induced production of TNF-α by peritoneal mast cells. Cytokine 18, 72-80. https://doi.org/10.1006/cyto.2002.0879
- Bai, D., Sun, T., Lu, F., Shen, Y., Zhang, Y., Zhang, B., Yu, G., Li, H. and Hao, J. (2022) Eupatilin suppresses OVA-induced asthma by inhibiting NF-κB and MAPK and activating Nrf2 signaling pathways in mice. Int. J. Mol. Sci. 23, 1582.
- Bakakos, A., Vogli, S., Dimakou, K. and Hillas, G. (2022) Asthma with fixed airflow obstruction: from fixed to personalized approach. J. Pers. Med. 12, 333.
- Barnes, P. J. (2013) Corticosteroid resistance in patients with asthma and chronic obstructive pulmonary disease. J. Allergy Clin. Immunol. 131, 636-645. https://doi.org/10.1016/j.jaci.2012.12.1564
- Bhavsar, P., Hew, M., Khorasani, N., Torrego, A., Barnes, P. J., Adcock, I. and Chung, K. F. (2008) Relative corticosteroid insensitivity of alveolar macrophages in severe asthma compared with non-severe asthma. Thorax 63, 784-790. https://doi.org/10.1136/thx.2007.090027
- Boudreau, R. T., Hoskin, D. W. and Lin, T. J. (2004) Phosphatase inhibition potentiates IL-6 production by mast cells in response to FcɛRI-mediated activation: involvement of p38 MAPK. J. Leukoc. Biol. 76, 1075-1081. https://doi.org/10.1189/jlb.1003498
- Breslow, D. K., Collins, S. R., Bodenmiller, B., Aebersold, R., Simons, K., Shevchenko, A., Ejsing, C. S. and Weissman, J. S. (2010) Orm family proteins mediate sphingolipid homeostasis. Nature 463, 1048-1053. https://doi.org/10.1038/nature08787
- Chen, C.-H., Zhang, D.-H., LaPorte, J. M. and Ray, A. (2000) Cyclic AMP activates p38 mitogen-activated protein kinase in Th2 cells: phosphorylation of GATA-3 and stimulation of Th2 cytokine gene expression. J. Immunol. 165, 5597-5605. https://doi.org/10.4049/jimmunol.165.10.5597
- Chiang, C.-Y., Chang, J.-H., Chuang, H.-C., Fan, C.-K., Hou, T.-Y., Lin, C.-L. and Lee, Y.-L. (2022) Schisandrin B promotes Foxp3+ regulatory T cell expansion by activating heme oxygenase-1 in dendritic cells and exhibits immunomodulatory effects in Th2-mediated allergic asthma. Eur. J. Pharmacol. 918, 174775.
- Collison, L. W., Chaturvedi, V., Henderson, A. L., Giacomin, P. R., Guy, C., Bankoti, J., Finkelstein, D., Forbes, K., Workman, C. J., Brown, S. A., Rehg, J. E., Jones, M. L., Ni, H. T., Artis, D., Turk, M. J. and Vignali, D. A. (2010) IL-35-mediated induction of a potent regulatory T cell population. Nat. Immunol. 11, 1093-1101. https://doi.org/10.1038/ni.1952
- Debeuf, N., Zhakupova, A., Steiner, R., Van Gassen, S., Deswarte, K., Fayazpour, F., Van Moorleghem, J., Vergote, K., Pavie, B., Lemeire, K., Hammad, H., Hornemann, T., Janssens, S. and Lambrecht, B. N. (2019) The ORMDL3 asthma susceptibility gene regulates systemic ceramide levels without altering key asthma features in mice. J. Allergy Clin. Immunol. 144, 1648-1659.e9. https://doi.org/10.1016/j.jaci.2019.06.041
- Escott, K., Belvisi, M., Birrell, M., Webber, S., Foster, M. and Sargent, C. (2000) Effect of the p38 kinase inhibitor, SB 203580, on allergic airway inflammation in the rat. Br. J. Pharmacol. 131, 173-176. https://doi.org/10.1038/sj.bjp.0703605
- Gilfillan, A. M., Peavy, R. D. and Metcalfe, D. D. (2009) Amplification mechanisms for the enhancement of antigen-mediated mast cell activation. Immunol. Res. 43, 15-24. https://doi.org/10.1007/s12026-008-8046-9
- Ha, S. G., Ge, X. N., Bahaie, N. S., Kang, B. N., Rao, A., Rao, S. P. and Sriramarao, P. (2013) ORMDL3 promotes eosinophil trafficking and activation via regulation of integrins and CD48. Nat. Commun. 4, 2479.
- Hale, K. K., Trollinger, D., Rihanek, M. and Manthey, C. L. (1999) Differential expression and activation of p38 mitogen-activated protein kinase α, β, γ, and δ in inflammatory cell lineages. J. Immunol. 162, 4246-4252. https://doi.org/10.4049/jimmunol.162.7.4246
- Heo, J., Shin, H., Lee, J., Kim, T., Inn, K.-S. and Kim, N.-J. (2015) Synthesis and biological evaluation of N-cyclopropylbenzamidebenzophenone hybrids as novel and selective p38 mitogen activated protein kinase (MAPK) inhibitors. Bioorg. Med. Chem. Lett. 25, 3694-3698. https://doi.org/10.1016/j.bmcl.2015.06.036
- Jarnicki, A. G., Conroy, H., Brereton, C., Donnelly, G., Toomey, D., Walsh, K., Sweeney, C., Leavy, O., Fletcher, J., Lavelle, E. C., Dunne, P. and Mills, K. H. (2008) Attenuating regulatory T cell induction by TLR agonists through inhibition of p38 MAPK signaling in dendritic cells enhances their efficacy as vaccine adjuvants and cancer immunotherapeutics. J. Immunol. 180, 3797-3806. https://doi.org/10.4049/jimmunol.180.6.3797
- Kalesnikoff, J., Huber, M., Lam, V., Damen, J. E., Zhang, J., Siraganian, R. P. and Krystal, G. (2001) Monomeric IgE stimulates signaling pathways in mast cells that lead to cytokine production and cell survival. Immunity 14, 801-811. https://doi.org/10.1016/S1074-7613(01)00159-5
- Kim, S. H., Jung, H. W., Kim, M., Moon, J. Y., Ban, G. Y., Kim, S. J., Yoo, H. J. and Park, H. S. (2020) Ceramide/sphingosine-1-phosphate imbalance is associated with distinct inflammatory phenotypes of uncontrolled asthma. Allergy 75, 1991-2004. https://doi.org/10.1111/all.14236
- Koprak, S., Staruch, M. J. and Dumont, F. J. (1999) A specific inhibitor of the p38 mitogen activated protein kinase affects differentially the production of various cytokines by activated human T cells: dependence on CD28 signaling and preferential inhibition of IL-10 production. Cell. Immunol. 192, 87-95. https://doi.org/10.1006/cimm.1998.1448
- Lee, J.-H. and Im, D.-S. (2021a) 4-CMTB ameliorates ovalbumininduced allergic asthma through FFA2 activation in mice. Biomol. Ther. (Seoul) 29, 427-433. https://doi.org/10.4062/biomolther.2020.176
- Lee, J. E. and Im, D. S. (2021b) Suppressive effect of carnosol on ovalbumin-induced allergic asthma. Biomol. Ther. (Seoul) 29, 58-63. https://doi.org/10.4062/biomolther.2020.050
- Li, W., Gao, R., Xin, T. and Gao, P. (2020) Different expression levels of interleukin-35 in asthma phenotypes. Respir. Res. 21, 89.
- Liu, W., Liang, Q., Balzar, S., Wenzel, S., Gorska, M. and Alam, R. (2008) Cell-specific activation profile of extracellular signal-regulated kinase 1/2, Jun N-terminal kinase, and p38 mitogen-activated protein kinases in asthmatic airways. J. Allergy Clin. Immunol. 121, 893-902.e2. https://doi.org/10.1016/j.jaci.2008.02.004
- Lu, B., Ferrandino, A. F. and Flavell, R. A. (2004) Gadd45β is important for perpetuating cognate and inflammatory signals in T cells. Nat. Immunol. 5, 38-44. https://doi.org/10.1038/ni1020
- Maneechotesuwan, K., Xin, Y., Ito, K., Jazrawi, E., Lee, K.-Y., Usmani, O. S., Barnes, P. J. and Adcock, I. M. (2007) Regulation of Th2 cytokine genes by p38 MAPK-mediated phosphorylation of GATA3. J. Immunol. 178, 2491-2498. https://doi.org/10.4049/jimmunol.178.4.2491
- Marzhan, K., Aidana, B. and Kh.S., O. (2022) Frequency of spread of bronchial asthma among middle-aged people and effectiveness of treatment. Almaty, City Clinical Hospital No. 1. World Science No 1(73). doi: 10.31435/rsglobal_ws/30012022/7747.
- Mikkelsen, S. S., Jensen, S. B., Chiliveru, S., Melchjorsen, J., Julkunen, I., Gaestel, M., Arthur, J. S. C., Flavell, R. A., Ghosh, S. and Paludan, S. R. (2009) RIG-I-mediated activation of p38 MAPK is essential for viral induction of interferon and activation of dendritic cells. J. Biol. Chem. 284, 10774-10782. https://doi.org/10.1074/jbc.M807272200
- Miller, M., Rosenthal, P., Beppu, A., Gordillo, R. and Broide, D. H. (2017) Oroscomucoid like protein 3 (ORMDL3) transgenic mice have reduced levels of sphingolipids including sphingosine-1-phosphate and ceramide. J. Allergy Clin. Immunol. 139, 1373-1376.e4. https://doi.org/10.1016/j.jaci.2016.08.053
- Miller, M., Rosenthal, P., Beppu, A., Mueller, J. L., Hoffman, H. M., Tam, A. B., Doherty, T. A., McGeough, M. D., Pena, C. A., Suzukawa, M., Niwa, M. and Broide, D. H. (2014) ORMDL3 transgenic mice have increased airway remodeling and airway responsiveness characteristic of asthma. J. Immunol. 192, 3475-3487. https://doi.org/10.4049/jimmunol.1303047
- Miller, M., Tam, A. B., Cho, J. Y., Doherty, T. A., Pham, A., Khorram, N., Rosenthal, P., Mueller, J. L., Hoffman, H. M., Suzukawa, M., Niwa, M. and Broide, D. H. (2012) ORMDL3 is an inducible lung epithelial gene regulating metalloproteases, chemokines, OAS, and ATF6. Proc. Natl. Acad. Sci. U.S.A. 109, 16648-16653. https://doi.org/10.1073/pnas.1204151109
- Moffatt, M. F., Kabesch, M., Liang, L., Dixon, A. L., Strachan, D., Heath, S., Depner, M., von Berg, A., Bufe, A., Rietschel, E., Heinzmann, A., Simma, B., Frischer, T., Willis-Owen, S. A., Wong, K. C., Illig, T., Vogelberg, C., Weiland, S. K., von Mutius, E., Abecasis, G. R., Farrall, M., Gut, I. G., Lathrop, G. M. and Cookson, W. O. (2007) Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature 448, 470-473. https://doi.org/10.1038/nature06014
- Mori, A., Kaminuma, O., Miyazawa, K., Ogawa, K., Okudaira, H. and Akiyama, K. (1999) p38 mitogen-activated protein kinase regulates human T cell IL-5 synthesis. J. Immunol. 163, 4763-4771. https://doi.org/10.4049/jimmunol.163.9.4763
- Nath, P., Leung, S.-Y., Williams, A., Noble, A., Chakravarty, S. D. S., Luedtke, G. R., Medicherla, S., Higgins, L. S., Protter, A. and Chung, K. F. (2006) Importance of p38 mitogen-activated protein kinase pathway in allergic airway remodelling and bronchial hyperresponsiveness. Eur. J. Pharmacol. 544, 160-167. https://doi.org/10.1016/j.ejphar.2006.06.031
- Ono, J. G., Kim, B. I., Zhao, Y., Christos, P. J., Tesfaigzi, Y., Worgall, T. S. and Worgall, S. (2020) Decreased sphingolipid synthesis in children with 17q21 asthma-risk genotypes. J. Clin. Invest. 130, 921-926. https://doi.org/10.1172/jci130860
- Oyeniran, C., Sturgill, J. L., Hait, N. C., Huang, W. C., Avni, D., Maceyka, M., Newton, J., Allegood, J. C., Montpetit, A., Conrad, D. H., Milstien, S. and Spiegel, S. (2015) Aberrant ORM (yeast)-like protein isoform 3 (ORMDL3) expression dysregulates ceramide homeostasis in cells and ceramide exacerbates allergic asthma in mice. J. Allergy Clin. Immunol. 136, 1035-1046.e6. https://doi.org/10.1016/j.jaci.2015.02.031
- Park, N., Park, S. J., Kim, M. H. and Yang, W. M. (2022) Efficacy and mechanism of essential oil from Abies holophylla leaf on airway inflammation in asthma: network pharmacology and in vivo study. Phytomedicine 96, 153898.
- Pelaia, C., Vatrella, A., Gallelli, L., Lombardo, N., Sciacqua, A., Savino, R. and Pelaia, G. (2021) Role of p38 mitogen-activated protein kinase in asthma and COPD: pathogenic aspects and potential targeted therapies. Drug Des. Devel. Ther. 15, 1275-1284. https://doi.org/10.2147/DDDT.S300988
- Qian, L., Xu, D., Xue, F., Li, M., Wang, X. and Liu, G. (2020) Inter-leukin-35 sensitizes monocytes from patients with asthma to glucocorticoid therapy by regulating p38 MAPK. Exp. Ther. Med. 19, 3247-3258.
- Rayees, S. and Din, I. (2021) Current asthma treatments. In Asthma: Pathophysiology, Herbal and Modern Therapeutic Interventions, pp. 19-25. Springer.
- Saklatvala, J. (2004) The p38 MAP kinase pathway as a therapeutic target in inflammatory disease. Curr. Opin. Pharmacol. 4, 372-377. https://doi.org/10.1016/j.coph.2004.03.009
- Schafer, P. H., Wadsworth, S. A., Wang, L. and Siekierka, J. J. (1999) p38α mitogen-activated protein kinase is activated by CD28-mediated signaling and is required for IL-4 production by human CD4+ CD45RO+ T cells and Th2 effector cells. J. Immunol. 162, 7110-7119. https://doi.org/10.4049/jimmunol.162.12.7110
- Siow, D., Sunkara, M., Dunn, T. M., Morris, A. J. and Wattenberg, B. (2015) ORMDL/serine palmitoyltransferase stoichiometry determines effects of ORMDL3 expression on sphingolipid biosynthesis. J. Lipid Res. 56, 898-908. https://doi.org/10.1194/jlr.M057539
- Skapenko, A., Lipsky, P. E., Kraetsch, H.-G., Kalden, J. R. and Schulze-Koops, H. (2001) Antigen-independent Th2 cell differentiation by stimulation of CD28: regulation via IL-4 gene expression and mitogen-activated protein kinase activation. J. Immunol. 166, 4283-4292. https://doi.org/10.4049/jimmunol.166.7.4283
- Tirpude, N. V., Sharma, A., Kumari, M. and Bhardwaj, N. (2022) Vitexin restores lung homeostasis by targeting vicious loop between inflammatory aggravation and autophagy mediated via multiple redox cascade and myeloid cells alteration in experimental allergic asthma. Phytomedicine 96, 153902.
- Underwood, D. C., Osborn, R. R., Kotzer, C. J., Adams, J. L., Lee, J. C., Webb, E. F., Carpenter, D. C., Bochnowicz, S., Thomas, H. C., Hay, D. W. and Griswold, D. E. (2000) SB 239063, a potent p38 MAP kinase inhibitor, reduces inflammatory cytokine production, airways eosinophil infiltration, and persistence. J. Pharmacol. Exp. Ther. 293, 281-288.
- Wallace-Farquharson, T., Rhee, H., Duckworth, L., Elder, J. H. and Wilkie, D. J. (2022) Children's and adolescents' descriptors of asthma symptoms: an integrative review. Int. J. Nurs. Stud. Adv. 4, 100063.
- Wang, Y., Yu, Y., Yu, W., Bian, X. and Gong, L. (2022) IL-35 inhibits cell pyroptosis and attenuates cell injury in TNF-α-induced bronchial epithelial cells via p38 MAPK signaling pathway. Bioengineered 13, 1758-1766. https://doi.org/10.1080/21655979.2021.2022266
- Worgall, T. S., Veerappan, A., Sung, B., Kim, B. I., Weiner, E., Bholah, R., Silver, R. B., Jiang, X.-C. and Worgall, S. (2013) Impaired sphingolipid synthesis in the respiratory tract induces airway hyperreactivity. Sci. Transl. Med. 5, 167-186.
- Zhakupova, A., Debeuf, N., Krols, M., Toussaint, W., Vanhoutte, L., Alecu, I., Kutalik, Z., Vollenweider, P., Ernst, D., von Eckardstein, A., Lambrecht, B. N., Janssens, S. and Hornemann, T. (2016) ORMDL3 expression levels have no influence on the activity of serine palmitoyltransferase. FASEB J. 30, 4289-4300. https://doi.org/10.1096/fj.201600639R