Skip to main content
Log in

Aryl hydrocarbon receptor (AhR) agonists increase airway epithelial matrix metalloproteinase activity

  • Original Article
  • Published:
Journal of Molecular Medicine Aims and scope Submit manuscript

Abstract

The aryl hydrocarbon receptor (AhR) agonists may upregulate matrix metalloproteinases (MMPs) and contribute to many airway diseases, such as asthma and chronic obstructive pulmonary disease. Elucidation of the detailed molecular mechanisms regulating MMPs may provide the scientific basis for diagnostic and therapeutic opportunities to improve the care of various pulmonary diseases, especially those related to xenobiotic agents. In this study, we investigated the detailed mechanisms of how AhR agonists modulated the expressions and activities of MMPs in bronchial epithelial cells. Treating the cells (Beas-2B or HBE135-E6E7) with 2-(1′H-indole-3′-carbonyl)-thiazole-4-carboxylic acid methyl ester or 2,3,7,8-tetrachlorodibenzo-p-dioxin, we found these AhR agonists increased the expression and activity of MMP-1 via a noncanonical AhR pathway and increased the activity of MMP-2 and MMP-9 in an MMP-1-dependent manner. AhR agonists increased the expression of MMP-1 via the activation of mitogen-activated protein kinase (MAPK) pathways by increased cytosolic calcium level and activated calcium/calmodulin-dependent protein kinase II (CaMKII). The activated MAPK pathways phosphorylated c-Jun, c-Fos, and ATF-2, resulting in their nuclear translocation and binding to the activator protein-1 (AP-1) elements of the MMP-1 promoter region. These findings correlated clinically to the significantly higher plasma/serum MMP-1 level in asthmatic patients. In conclusion, the present study demonstrated a novel signaling pathway by which AhR agonists elevated intracellular calcium levels, which activated CaMKII, leading to increased MMP-1 expression through MAPK pathways in bronchial epithelial cell lines. This novel regulatory pathway may serve as a potential target for the treatment of airway remodeling of many pulmonary diseases, such as asthma.

Key message

  • AhR agonists increase MMP-1 expression in bronchial epithelial cells.

  • The underlying AhR pathway involves CaMKII, MAPKs, and AP-1 elements.

  • The upregulated MMP-1 further activated MMP-2 and MMP-9.

  • Asthmatic patients have higher serum MMP-1 level.

  • This novel regulatory pathway is a potential target for treating asthma.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  1. Kung T, Murphy KA, White LA (2009) The aryl hydrocarbon receptor (AhR) pathway as a regulatory pathway for cell adhesion and matrix metabolism. Biochem Pharmacol 77:536–546

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  2. Dietrich C, Kaina B (2010) The aryl hydrocarbon receptor (AhR) in the regulation of cell-cell contact and tumor growth. Carcinogenesis 31:1319–1328

    Article  CAS  PubMed  Google Scholar 

  3. Song J, Clagett-Dame M, Peterson RE, Hahn ME, Westler WM, Sicinski RR, DeLuca HF (2002) A ligand for the aryl hydrocarbon receptor isolated from lung. Proc Natl Acad Sci U S A 99:14694–14699

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Henry EC, Bemis JC, Henry O, Kende AS, Gasiewicz TA (2006) A potential endogenous ligand for the aryl hydrocarbon receptor has potent agonist activity in vitro and in vivo. Arch Biochem Biophys 450:67–77

    Article  CAS  PubMed  Google Scholar 

  5. Tan Z, Chang X, Puga A, Xia Y (2002) Activation of mitogen-activated protein kinases (MAPKs) by aromatic hydrocarbons: role in the regulation of aryl hydrocarbon receptor (AHR) function. Biochem Pharmacol 64:771–780

    Article  CAS  PubMed  Google Scholar 

  6. Wong PS, Vogel CF, Kokosinski K, Matsumura F (2010) Arylhydrocarbon receptor activation in NCI-H441 cells and C57BL/6 mice: possible mechanisms for lung dysfunction. Am J Respir Cell Mol Biol 42:210–217

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  7. Carver LA, Hogenesch JB, Bradfield CA (1994) Tissue specific expression of the rat Ah-receptor and ARNT mRNAs. Nucleic Acids Res 22:3038–3044

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  8. Turner MC, Krewski D, Pope CA 3rd, Chen Y, Gapstur SM, Thun MJ (2011) Long-term ambient fine particulate matter air pollution and lung cancer in a large cohort of never-smokers. Am J Respir Crit Care Med 184:1374–1381

    Article  PubMed  Google Scholar 

  9. Chiba T, Uchi H, Yasukawa F, Furue M (2011) Role of the arylhydrocarbon receptor in lung disease. Int Arch Allergy Immunol 155(Suppl 1):129–134

    Article  CAS  PubMed  Google Scholar 

  10. Vignola AM, Riccobono L, Mirabella A, Profita M, Chanez P, Bellia V, Mautino G, D’Accardi P, Bousquet J, Bonsignore G (1998) Sputum metalloproteinase-9/tissue inhibitor of metalloproteinase-1 ratio correlates with airflow obstruction in asthma and chronic bronchitis. Am J Respir Crit Care Med 158:1945–1950

    Article  CAS  PubMed  Google Scholar 

  11. Prikk K, Maisi P, Pirila E, Reintam MA, Salo T, Sorsa T, Sepper R (2002) Airway obstruction correlates with collagenase-2 (MMP-8) expression and activation in bronchial asthma. Lab Invest 82:1535–1545

    Article  CAS  PubMed  Google Scholar 

  12. Huang CD, Lin SM, Chang PJ, Liu WT, Wang CH, Liu CY, Lin HC, Hsieh LL, Kuo HP (2009) Matrix metalloproteinase-1 polymorphism is associated with persistent airway obstruction in asthma in the Taiwanese population. J Asthma 46:41–46

    Article  CAS  PubMed  Google Scholar 

  13. Crosby LM, Waters CM (2010) Epithelial repair mechanisms in the lung. Am J Physiol Lung Cell Mol Physiol 298:L715–L731

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  14. Ohbayashi H (2002) Matrix metalloproteinases in lung diseases. Curr Protein Pept Sci 3:409–421

    Article  CAS  PubMed  Google Scholar 

  15. Segura-Valdez L, Pardo A, Gaxiola M, Uhal BD, Becerril C, Selman M (2000) Upregulation of gelatinases A and B, collagenases 1 and 2, and increased parenchymal cell death in COPD. Chest 117:684–694

    Article  CAS  PubMed  Google Scholar 

  16. Mercer BA, Wallace AM, Brinckerhoff CE, D’Armiento JM (2009) Identification of a cigarette smoke-responsive region in the distal MMP-1 promoter. Am J Respir Cell Mol Biol 40:4–12

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  17. Imai K, Dalal SS, Chen ES, Downey R, Schulman LL, Ginsburg M, D’Armiento J (2001) Human collagenase (matrix metalloproteinase-1) expression in the lungs of patients with emphysema. Am J Respir Crit Care Med 163:786–791

    Article  CAS  PubMed  Google Scholar 

  18. Wygrecka M, Wilhelm J, Jablonska E, Zakrzewicz D, Preissner KT, Seeger W, Guenther A, Markart P (2011) Shedding of low-density lipoprotein receptor-related protein-1 in acute respiratory distress syndrome. Am J Respir Crit Care Med 184:438–448

    Article  CAS  PubMed  Google Scholar 

  19. Torii K, Iida K, Miyazaki Y, Saga S, Kondoh Y, Taniguchi H, Taki F, Takagi K, Matsuyama M, Suzuki R (1997) Higher concentrations of matrix metalloproteinases in bronchoalveolar lavage fluid of patients with adult respiratory distress syndrome. Am J Respir Crit Care Med 155:43–46

    Article  CAS  PubMed  Google Scholar 

  20. Martinez JM, Afshari CA, Bushel PR, Masuda A, Takahashi T, Walker NJ (2002) Differential toxicogenomic responses to 2,3,7,8-tetrachlorodibenzo-p-dioxin in malignant and nonmalignant human airway epithelial cells. Toxicol Sci 69:409–423

    Article  CAS  PubMed  Google Scholar 

  21. Wang TN, Lin MC, Wu CC, Leung SY, Huang MS, Chuang HY, Lee CH, Wu DC, Ho PS, Ko AM et al (2010) Risks of exposure to occupational asthmogens in atopic and nonatopic asthma: a case–control study in Taiwan. Am J Respir Crit Care Med 182:1369–1376

    Article  CAS  PubMed  Google Scholar 

  22. Cataldo D, Munaut C, Noel A, Frankenne F, Bartsch P, Foidart JM, Louis R (2000) MMP-2- and MMP-9-linked gelatinolytic activity in the sputum from patients with asthma and chronic obstructive pulmonary disease. Int Arch Allergy Immunol 123:259–267

    Article  CAS  PubMed  Google Scholar 

  23. Chakraborti S, Mandal M, Das S, Mandal A, Chakraborti T (2003) Regulation of matrix metalloproteinases: an overview. Mol Cell Biochem 253:269–285

    Article  CAS  PubMed  Google Scholar 

  24. Volman TJ, Goris RJ, Lomme RM, DeGroot J, Verhofstad AA, Hendriks T (2004) Increased expression of matrix metalloproteinases in the murine zymosan-induced multiple organ dysfunction syndrome. J Pathol 203:968–975

    Article  CAS  PubMed  Google Scholar 

  25. Puga A, Ma C, Marlowe JL (2009) The aryl hydrocarbon receptor cross-talks with multiple signal transduction pathways. Biochem Pharmacol 77:713–722

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  26. Puga A, Hoffer A, Zhou S, Bohm JM, Leikauf GD, Shertzer HG (1997) Sustained increase in intracellular free calcium and activation of cyclooxygenase-2 expression in mouse hepatoma cells treated with dioxin. Biochem Pharmacol 54:1287–1296

    Article  CAS  PubMed  Google Scholar 

  27. Monteiro P, Gilot D, Le Ferrec E, Rauch C, Lagadic-Gossmann D, Fardel O (2008) Dioxin-mediated up-regulation of aryl hydrocarbon receptor target genes is dependent on the calcium/calmodulin/CaMKIalpha pathway. Mol Pharmacol 73:769–777

    Article  CAS  PubMed  Google Scholar 

  28. Chen S, Xu Y, Xu B, Guo M, Zhang Z, Liu L, Ma H, Chen Z, Luo Y, Huang S et al (2011) CaMKII is involved in cadmium activation of MAPK and mTOR pathways leading to neuronal cell death. J Neurochem 119:1108–1118

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  29. Cataldo DD, Gueders M, Munaut C, Rocks N, Bartsch P, Foidart JM, Noel A, Louis R (2004) Matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases mRNA transcripts in the bronchial secretions of asthmatics. Lab Invest 84:418–424

    Article  CAS  PubMed  Google Scholar 

  30. Villano CM, Murphy KA, Akintobi A, White LA (2006) 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces matrix metalloproteinase (MMP) expression and invasion in A2058 melanoma cells. Toxicol Appl Pharmacol 210:212–224

    Article  CAS  PubMed  Google Scholar 

  31. Murphy KA, Villano CM, Dorn R, White LA (2004) Interaction between the aryl hydrocarbon receptor and retinoic acid pathways increases matrix metalloproteinase-1 expression in keratinocytes. J Biol Chem 279:25284–25293

    Article  CAS  PubMed  Google Scholar 

  32. Suzuki R, Kato T, Miyazaki Y, Iwata M, Noda Y, Takagi K, Nakashima N, Torii K (2001) Matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases in sputum from patients with bronchial asthma. J Asthma 38:477–484

    Article  CAS  PubMed  Google Scholar 

  33. Kelly EA, Busse WW, Jarjour NN (2000) Increased matrix metalloproteinase-9 in the airway after allergen challenge. Am J Respir Crit Care Med 162:1157–1161

    Article  CAS  PubMed  Google Scholar 

  34. Tanaka H, Miyazaki N, Oashi K, Tanaka S, Ohmichi M, Abe S (2000) Sputum matrix metalloproteinase-9: tissue inhibitor of metalloproteinase-1 ratio in acute asthma. J Allergy Clin Immunol 105:900–905

    Article  CAS  PubMed  Google Scholar 

  35. Mattos W, Lim S, Russell R, Jatakanon A, Chung KF, Barnes PJ (2002) Matrix metalloproteinase-9 expression in asthma: effect of asthma severity, allergen challenge, and inhaled corticosteroids. Chest 122:1543–1552

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The authors thank the Center for Research Resources and Development at Kaohsiung Medical University for the instrumental support of confocal microscope. The authors also appreciate the careful review and precious comments from the editors and reviewers.

This study was supported by grants from the Kaohsiung Medical University Hospital (KMUH99-9I08, KMUH101-1M12 and KMUH102-2T06), National Science Council (NSC 101-2320-B-037-043-MY3) and National Health Research Institutes (NHRI-100A1-PDCO-03000001 and NHRI-101A1-PDCO-03010201).

Conflict of interest

The authors declare no conflicts of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ming-Shyan Huang.

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM 1

(PDF 311 kb)

(AVI 5,375 kb)

(AVI 5,375 kb)

(AVI 5,375 kb)

(AVI 5,375 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tsai, MJ., Hsu, YL., Wang, TN. et al. Aryl hydrocarbon receptor (AhR) agonists increase airway epithelial matrix metalloproteinase activity. J Mol Med 92, 615–628 (2014). https://doi.org/10.1007/s00109-014-1121-x

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00109-014-1121-x

Keywords

Navigation