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. 2012 Aug 17;303(8):H919–H930. doi: 10.1152/ajpheart.00577.2012

Table 2.

A selection of MMP and TIMP null phenotypes in mice

MMP Phenotypes
-1a* ↓ Angiogenesis; ↓ tumors
-2 ↑ Tumor cell apoptosis
-3 ↓ Angiogenesis; ↓ tumors
-7 ↓ Intestinal adenoma formation
-8 ↑ Skin tumors; ↑ response in arthritis; ↓ lung fibrosis
-9 ↓ MMP-2 expression, ↓ SMC migration and neovascularization
-10 ↑ Inflammation to Pseudomonas aeruginosa infection
-11 Accelerated neointima formation in vascular injury model
-12 Early pulmonary fibrosis and ↓ airway resistance
-13 ↑ Interstitial collagen; defect in growth plate cartilage
-14 Arthritis; osteopenia; dwarfism; ↓ macrophage infiltration
-16 ↓ Growth, ↓ mesenchymal cell viability
-19 Obesity; ↑ tenascin C; ↑ Th2 inflammation
-20 Decreased mineral content; deteriorating enamel organ morphology
-24 Abnormal mast cell degranulation
-15, -17, -21, -23, -25, -27 Mouse model available but phenotype not yet published or observed
-1b*, -18, -22, -26 Mouse model not available
-28 ↑ Inflammation and ECM response to cardiac aging
TIMP-1 ↑ Remodeling post-myocardial infarction, ↓ adipose in high-fat diet
TIMP-2 Delayed neuronal differentiation, weak muscles
TIMP-3 Left ventricular dilation, cardiomyocyte hypertrophy
TIMP-4 ↑ neutrophil infiltration

Of note, most MMP null mice are viable and fertile and show phenotypes only under stressed conditions (17, 19, 34, 47, 49, 53, 68, 69, 74, 92, 99, 121, 124, 133, 164).

*

There are two MMP-1 genes in mice. *There are two MMP-1 genes in mice, which are MMP-1a and MMP-1b. SMC, smooth muscle cell; Th2, T-helper 2.