Revisiting matrix metalloproteinase 12: its role in pathophysiology of asthma and related pulmonary diseases

. 2021 Jan ; 27 (1) : 54-60.

Jazyk angličtina Země Spojené státy americké Médium print

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid33065600
Odkazy

PubMed 33065600
DOI 10.1097/mcp.0000000000000743
PII: 00063198-202101000-00010
Knihovny.cz E-zdroje

PURPOSE OF REVIEW: Matrix metalloproteinases (MMPs) are a family of over 20 zinc-dependent proteases with different biological and pathological activities, and many have been implicated in several diseases. Although nonselective MMP inhibitors are known to induce serious side-effects, targeting individual MMPs may offer a safer therapeutic potential for several diseases. Hence, we provide a concise overview on MMP-12, given its association with pulmonary diseases, including asthma, chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis, and other progressive pulmonary fibrosis (PPF), which may also occur in coronavirus disease 2019. RECENT FINDINGS: In asthma, COPD, and PPF, increased MMP-12 levels have been associated with inflammation and/or structural changes within the lungs and negatively correlated with functional parameters. Increased pulmonary MMP-12 levels and MMP-12 gene expression have been related to disease severity in asthma and COPD. Targeting MMP-12 showed potential in animal models of pulmonary diseases but human data are still very scarce. SUMMARY: Although there may be a potential role of MMP-12 in asthma, COPD and PPF, several pathophysiological aspects await elucidation. Targeting MMP-12 may provide further insights into MMP-12 related mechanisms and how this translates into clinical outcomes; this warrants further research.

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Nagase H, Visse R, Murphy G. Structure and function of matrix metalloproteinases and TIMPs. Cardiovasc Res 2006; 69:562–573.

Vandenbroucke R, Libert C. Is there new hope for therapeutic matrix metalloproteinase inhibition? Nat Rev Drug Discov 2014; 13:904–927.

Löffek S, Schilling O, Franzke CW. Biological role of matrix metalloproteinases: a critical balance. Eur Respir J 2011; 38:191–208.

Hu J, Van den Steen PE, Sang QX, Opdenakker G. Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases. Nat Rev Drug Discov 2007; 6:480–498.

Cavalla F, Hernández-Ríos P, Sorsa T, et al. Matrix Metalloproteinases as Regulators of Periodontal inflammation. Int J Mol Sci 2017; 18:440.

Leeming D, Sand J, Nielsen M, et al. Serological investigation of the collagen degradation profile of patients with chronic obstructive pulmonary disease or idiopathic pulmonary fibrosis. Biomark Insights 2012; 7:119–126.

Johnson S, Knox A. Autocrine production of matrix metalloproteinase-2 is required for human airway smooth muscle proliferation. Am J Physiol 1999; 277 (6 Pt 1):L1109–L1117.

Hiraoka N, Allen E, Apel IJ, et al. Matrix metalloproteinases regulate neovascularization by acting as pericellular fibrinolysins. Cell 1998; 95:365–377.

Oikonomidi S, Kostikas K, Tsilioni I. Matrix metalloproteinases in respiratory diseases: from pathogenesis to potential clinical implications. Curr Med Chem 2009; 16:1214–1228.

Vandenbroucke R, Dejonckheere E, Libert C. A therapeutic role for matrix metalloproteinase inhibitors in lung diseases. Eur Respir J 2011; 38:1200–1214.

Barton A, Gehlen H. Pulmonary remodeling in equine asthma: what do we know about mediators of inflammation in the horse? Mediators Inflamm 2016; 2016:5693205.

Hikichi M, Mizumura K, Maruoka S, et al. Pathogenesis of chronic obstructive pulmonary disease (COPD) induced by cigarette smoke. J Thorac Dis 2019; 11: (Suppl. 17): S2129–S2140.

Roque W, Boni A, Martinez-Manzano J, Romero F. A tale of two proteolytic machines: matrix metalloproteinases and the ubiquitin-proteasome system in pulmonary fibrosis. Int J Mol Sci 2020; 21:3878.

Shen KH, Hung JH, Liao YC, et al. Sinomenine inhibits migration and invasion of human lung cancer cell through downregulating expression of miR-21 and MMPs. Int J Mol Sci 2020; 21:3080.

Hendrix AY, Kheradmand F. The role of matrix metalloproteinases in development, repair, and destruction of the lungs. Prog Mol Biol Transl Sci. 2017; 148:1-29.

Solun B, Shoenfeld Y. Inhibition of metalloproteinases in therapy for severe lung injury due to COVID-19. Med Drug Discov 2020; 7:100052.

Page-McCaw A, Ewald A, Werb Z. Matrix metalloproteinases and the regulation of tissue remodeling. Nat Rev Mol Cell Biol 2007; 8:221–233.

Lagente V, Le Quement C, Boichot E. Macrophage metalloelastase (MMP-12) as a target for inflammatory respiratory diseases. Expert Opin Ther Targets 2009; 13:287–295.

Brusselle G. Matrix metalloproteinase 12, asthma, and COPD. N Engl J Med 2009; 361:2664–2665.

Molet S, Belleguic C, Lena H, et al. Increase in macrophage elastase (MMP-12) in lungs from patients with chronic obstructive pulmonary disease. Inflamm Res 2005; 54:31–36.

Dancer R, Wood A, Thickett D. Metalloproteinases in idiopathic pulmonary fibrosis. Eur Respir J 2011; 38:1461–1467.

Vaalamo M, Kariniemi AL, Shapiro SD, Saarialho-Kere U. Enhanced expression of human metalloelastase (MMP-12) in cutaneous granulomas and macrophage migration. J Investig Dermatol 1999; 112:499–505.

Suomela S, Kariniemi AL, Snellman E, Saarialho-Kere U. Metalloelastase (MMP-12) and 92-kDa gelatinase (MMP-9) as well as their inhibitors, TIMP-1 and -3, are expressed in psoriatic lesions. Exp Dermatol 2001; 10:175–183.

Chen Y. MMP-12, an old enzyme plays a new role in the pathogenesis of rheumatoid arthritis? Am J Pathol 2004; 165:1069–1070.

Kader A, Shao L, Dinney C, et al. Matrix metalloproteinase polymorphisms and bladder cancer risk. Cancer Res 2006; 66:11644–11648.

Qu P, Du H, Wang X, Yan C. Matrix metalloproteinase 12 overexpression in lung epithelial cells plays a key role in emphysema to lung bronchioalveolar adenocarcinoma transition. Cancer Res 2009; 69:7252–7261.

Shin A, Cai Q, Shu XO, et al. Genetic polymorphisms in the matrix metalloproteinase 12 gene (MMP12) and breast cancer risk and survival: the Shanghai Breast Cancer Study. Breast Cancer Res 2005; 7:R506–R512.

Liang J, Liu E, Yu Y, et al. Macrophage metalloelastase accelerates the progression of atherosclerosis in transgenic rabbits. Circulation 2006; 113:1993–2001.

Curci J, Liao S, Huffman M, et al. Expression and localization of macrophage elastase (matrix metalloproteinase-12) in abdominal aortic aneurysms. J Clin Invest 1998; 102:1900–1910.

Gu BH, Choi J, Shen Y, et al. Elastin-specific autoimmunity in smokers with thoracic aortic aneurysm and dissection is independent of chronic obstructive pulmonary disease. J Am Heart Assoc 2019; 8:e011671.

Wells J, Rice T, Nuttall R, et al. An adverse role for matrix metalloproteinase 12 after spinal cord injury in mice. J Neurosci 2003; 23:10107–10115.

Vos C, van Haastert E, de Groot C, et al. Matrix metalloproteinase-12 is expressed in phagocytotic macrophages in active multiple sclerosis lesions. J Neuroimmunol 2003; 138 (1–2):106–114.

Power C, Henry S, Del Bigio M, et al. Intracerebral hemorrhage induces macrophage activation and matrix metalloproteinases. Ann Neurol 2003; 53:731–742.

Chelluboina B, Klopfenstein JD, Pinson DM, et al. Matrix metalloproteinase-12 induces blood-brain barrier damage after focal cerebral ischemia. Stroke 2015; 46:3523–3531.

Belvisi M, Bottomley K. The role of matrix metalloproteinases (MMPs) in the pathophysiology of chronic obstructive pulmonary disease (COPD): a therapeutic role for inhibitors of MMPs? Inflamm Res 2003; 52:95–100.

Hautamaki R, Kobayashi D, Senior R, Shapiro S. Requirement for macrophage elastase for cigarette smoke-induced emphysema in mice. Science 1997; 277:2002–2004.

Churg A, Zhou S, Wright J. Matrix metalloproteinases in COPD. Eur Respir J 2012; 39:197–209.

Demedts I, Morel-Montero A, Lebecque S, et al. Elevated MMP-12 protein levels in induced sputum from patients with COPD. Thorax 2006; 61:196–201.

Shibata S, Miyake K, Tateishi T, et al. Basophils trigger emphysema development in a murine model of COPD through IL-4-mediated generation of MMP-12-producing macrophages. PNAS 2018; 115:13057–13062.

Vieira C, Oliveira L, Da Silva M, et al. Role of metalloproteinases and TNF-α in obesity-associated asthma in mice. Life Sci 2020; 259:118191.

Haq I, Chappell S, Johnson S, et al. Association of MMP-12 polymorphisms with severe and very severe COPD: a case control study of MMP-1, 9 and 12 in a European population. BMC Med Genet 2010; 11:7.

Chaudhuri R, McSharry C, Brady J, et al. Sputum matrix metalloproteinase-12 in patients with chronic obstructive pulmonary disease and asthma: relationship to disease severity. J Allergy Clin Immunol 2012; 129:655–663.e8.

Gottlieb D, Stone P, Sparrow D, et al. Urinary desmosine excretion in smokers with and without rapid decline of lung function: the Normative Aging Study. Am J Respir Crit Care Med 1996; 154:1290–1295.

Doyle AD, Mukherjee M, LeSuer WE, et al. Eosinophil-derived IL-13 promotes emphysema. Eur Respir J 2019; 53:1801291pii: 1801291.

Hinks T, Brown T, Lau L, et al. Multidimensional endotyping in patients with severe asthma reveals inflammatory heterogeneity in matrix metalloproteinases and chitinase 3-like protein 1. J Allergy Clin Immunol 2016; 138:61–75.

Yamaide F, Undarmaa S, Mashimo Y, et al. Association study of matrix metalloproteinase-12 gene polymorphisms and asthma in a Japanese population. Int Arch Allergy Immunol 2013; 160:287–296.

Mukhopadhyay S, Sypek J, Tavendale R, et al. Matrix metalloproteinase-12 is a therapeutic target for asthma in children and young adults. J Allergy Clin Immunol 2010; 126:70–76. e16.

Manoury B, Nenan S, Guenon I, et al. Macrophage metalloelastase (MMP-12) deficiency does not alter bleomycin-induced pulmonary fibrosis in mice. J Inflamm (Lond) 2006; 3:2.

Matute-Bello G, Wurfel M, Lee J, et al. Essential role of MMP-12 in Fas-induced lung fibrosis. Am J Respir Cell Mol Biol 2007; 37:210–221.

Todd J, Vinisko R, Liu Y, et al. Circulating matrix metalloproteinases and tissue metalloproteinase inhibitors in patients with idiopathic pulmonary fibrosis in the multicenter IPF-PRO Registry cohort. BMC Pulm Med 2020; 20:64.

Manetti M, Guiducci S, Romano E, et al. Increased serum levels and tissue expression of matrix metalloproteinase-12 in patients with systemic sclerosis: correlation with severity of skin and pulmonary fibrosis and vascular damage. Ann Rheum Dis 2012; 71:1064–1072.

Hu B, Wu Z, Bai D, et al. Matrix metalloproteinase-12 (MMP12) inhibits myofibroblast differentiation and lung fibrosis. Fasebj 2015; Volume29, IssueS1. Experimental Biology 2015 Meeting Abstracts. 2015; 411.6.

Gupta A, Madhavan MV, Sehgal K, et al. Extrapulmonary manifestations of COVID-19. Nat Med 2020; 26:1017–1032.

Lai C, Ko W, Lee P, et al. Extra-respiratory manifestations of COVID-19. Int J Antimicrob Agents 2020; 56:106024.

Yu N, Shen C, Yu Y, et al. Lung involvement in patients with coronavirus disease-19 (COVID-19): a retrospective study based on quantitative CT findings. Chin J Acad Radiol 2020; 1–6.

Tuttolomondo D, Frizzelli A, Aiello M, et al. Beyond the lung involvement in COVID-19 patients. A review. Minerva Med 2020; doi: 10.23736/S0026-4806.20.06719-1. Online ahead of print. DOI

Jesenak M, Banovcin P, Diamant Z. COVID-19, chronic inflammatory respiratory diseases and eosinophils: observations from reported clinical case series. Allergy 2020; 5:1819–1822.

Jesenak M, Brndiarova M, Urbancikova I, et al. Immune parameters and COVID-19 infection: association with clinical severity and disease prognosis. Front Cell Infect Microbiol 2020; 10:364.

Lippi G, Plebani M. Laboratory abnormalities in patients with COVID-19 infection. Clin Chem Lab Med 2020; 58:1131–1134.

Xu Z, Shi L, Wang Y, et al. Pathological findings of COVID-19 associated with acute respiratory distress syndrome. Lancet Respir Med 2020; 8:420–422.

Potus F, Mai V, Lebret M, et al. Novel insights on the pulmonary vascular consequences of COVID-19. Am J Physiol Lung Cell Mol Physiol 2020; 319:L277–L288.

George P, Wells A, Jenkins R. Pulmonary fibrosis and COVID-19: the potential role for antifibrotic therapy. Lancet Respir Med 2020; 8:807–815.

Davey A, McAuley DF, O’Kane CM. Matrix metalloproteinases in acute lung injury: mediatros of injury and drivers of repair. Eur Respir J 2011; 38:959–970.

Gharib S, Manicone A, Parks W. Matrix metalloproteinases in emphysema. Matrix Biol 2018; 73:34–51.

Tomar B, Anders H, Desai J, Mulay S. Neutrophils and neutrophil extracellular traps drive necroinflammation in COVID-19. Cells 2020; 9:1383.

Pouladi M, Robbins C, Swirski F, et al. Interleukin-13-dependent expression of matrix metalloproteinase-12 is required for the development of airway eosinophilia in mice. Am J Respir Cell Mol Biol 2004; 30:84–90.

Xie S, Issa R, Sukkar M, et al. Induction and regulation of matrix metalloproteinase-12 in human airway smooth muscle cells. Respir Res 2005; 6:148.

Del Valle D, Kim-Schulze S, Huang H-H, et al. An inflammatory cytokine signature predicts COVID-19 severity and survival. Nature Med 2020; 26:1636–1643.

Dofferhoff A, Piscaer I, Schurgers L, et al. Reduced vitamin K status as a potentially modifiable risk factor of severe COVID-19. Clin Infect Dis 2020; ciaa1258. doi: 10.1093/cid/ciaa1258. Online ahead of print. DOI

Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 2020; 395:497–506.

Liu Y, Zhang F, Huang F, et al. 2019-novel coronavirus (2019-nCov) infections trigger an exaggerated cytokine response aggravating lung injury. 2020; http://www.chinaxiv.org/abs/202002.00018v1 . Online ahead of print.

Donlan A, Young M, Petri W, Abhyankar M. IL-13 predicts the need for mechanical ventilation in COVID-10 patients. MedRxiv 2020; doi: 10.1101/2020.06.18.20134353. Online ahead of print. DOI

Shi S, Su M, Shen G, et al. Matrix metalloproteinase 3 as a valuable marker for patients with COVID-19. J Med Virol 2020; doi:10.1002/jmv.26235. DOI

Ueland T, Holter J, Holten A, et al. Distinct and early increase in circulating MMP-9 in COVID-19 patients with respiratory failure. J Infect 2020; 81:e41–e43.

Desforges M, Miletti T, Gagnon M, Talbot P. Activation of human monocytes after infection by human coronavirus 229E. Virus Res 2007; 130:228–240.

Wolf M, Clay S, Zheng S, et al. MMP12 inhibits corneal neovascularization and inflammation through regulation of CCL2. Scientific Reports 2019; 9:11579.

Marchant D, Bellac C, Moraes T, et al. A new transcriptional role for matrix metalloproteinase-12 in antiviral immunity. Nature Med 2014; 20:493–502.

Magnussen H, Watz H, Kirsten A, et al. Safety and tolerability of an oral MMP-9 and -12 inhibitor, AZD1236, in patients with moderate-to-severe COPD: a randomised controlled 6-week trial. Pulm Pharmacol Ther 2011; 24:563–570.

Dahl R, Titlestad I, Lindqvist A, et al. Effects of an oral MMP-9 and -12 inhibitor, AZD1236, on biomarkers in moderate/severe COPD: a randomised controlled trial. Pulm Pharmacol Ther 2012; 25:169–177.

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