Table 1– Phenotype of matrix metalloproteinase (MMP)-deficient mice in different lung pathologies
Lung pathologyDeficiencyObservations[Ref.]
COPDCigarette smoke exposureMMP12Decreased inflammation, neutrophil influx and emphysema in the lung[13, 14]
MMP9Normal development of cigarette smoke-induced inflammation and airspace enlargement compared[15]
AsthmaAspergillus fumigatus and OVAMMP9Disrupted trafficking of neutrophils and eosinophils into the BALF[16]
Massive accumulation of apoptotic cells in the lungs
OVAIncreased airway inflammation[17]
German cockroach frassIncreased airway inflammation[18]
OVAImpaired cellular infiltration and bronchial hyperresponsiveness[19]
OVAImpaired accumulation of airway wall dendritic cells[20]
Aspergillus fumigatus and OVAMMP2Disrupted trafficking of eosinophils into the BALF[16, 21]
Massive accumulation of apoptotic cells in the lungs
Increased susceptibility to asphyxiation
Aspergillus fumigatus and OVAMMP9/MMP2MMP9 is the dominant airway MMP controlling inflammatory cell egression[16]
Cockroach antigenMMP12Reduced inflammatory injury[22]
House miteMMP8Airway hyperresponsiveness and decreased levels of soluble IL-13Rα2[23]
ILDBleomycinMMP8Less fibrosis[24]
Decreased IL-10 processing
BleomycinMMP12No effect[25]
Fas-activating monoclonal antibodyDecreased expression of profibrotic genes[26]
BleomycinMMP9Reduced alveolar bronchiolisation[27]
BleomycinMMP7Impaired efflux of neutrophils into the alveolar space[28]
Reduced lethality
Decreased alveolar fibrosis at later stages
BleomycinReduced fibrosis[29]
ALIHigh-pressure ventilationMMP8Decreased lung oedema and permeability[30]
Diminished histological injury
Mechanical ventilationIncreased alveolar permeability[31]
LPSAccumulation of PMN cells in alveolar space[32]
BleomycinAccumulation of PMN cells in alveolar space[33]
Increased alveolar capillary barrier injury
Increased lung elastance
Increased mortality
LPSMMP9No protection[34]
Development of emphysema
OzoneIncreased protein content and numbers of neutrophils and epithelial cells in BALF[35]
Increased KC and MIP2 levels in BALF
OzoneMMP7No effect[35]
HyperoxiaMMP13Increased inflammation because of the lack of MCP1 cleavage[36]
Immunoglobulin G immune complexMMP3Reduced lung injury[37]
Reduction in leukocyte recruitment
Lung cancerMMTV-PyMTMMP13No effect on development of lung metastasis[38]
B16-BL6 melanomaMMP9Reduced number of metastatic colonies[39]
Lewis lung carcinoma
MMTV-PyVTDecreased angiogenesis[40]
Decrease in lung tumour burden
MMTV-PyVTMMP7No effect on development of lung metastases[40]
B16-BL6 melanomaMMP2Reduced tumour-induced angiogenesis[41]
Lewis lung carcinoma
Lewis lung carcinomaMMP12Increased number of pulmonary metastases[42]
BOSHeterotopic airway transplant modelMMP8Reduced neutrophil influx and collagen deposition[43]
Heterotopic murine tracheal allograftsMMP9Reduced neutrophil influx and collagen deposition[44]
CLDPulmonary overexpression of human mature IL-1βMMP9Increased IL-1β-induced lung injury[45]
  • COPD: chronic obstructive pulmonary disease; ILD: interstitial lung diseases; ALI: acute lung injury; BOS: bronchiolitis obliterans syndrome; CLD: chronic lung disease of prematurity; OVA: ovalbumin; BALF: bronchoalveolar lavage fluid; IL: interleukin; LPS: lipopolysaccharide; PMN: polymorphonuclear; KC: keratinocyte chemoattractant; MIP2: macrophage inflammatory protein-2; MCP1: monocyte chemoattractant protein-1; MMTV-PyMT, MMTV-PyVT: mouse mammary tumour virus with polyoma middle T-antigen promoter, mouse mammary tumour virus.