Temporal and Topographic Matrix Metalloproteinase Expression after Vascular Injury in Mice

H. R. Lijnen; F. Lupu; L. Moons; P. Carmeliet; D. Goulding; D. Collen

doi:10.1055/s-0037-1614573

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 1999; 81(05): 799-807
DOI: 10.1055/s-0037-1614573

Rapid Communication

Schattauer GmbH

Temporal and Topographic Matrix Metalloproteinase Expression after Vascular Injury in Mice

H. R. Lijnen

¹From the Center for Molecular and Vascular Biology, University of Leuven, Belgium

,

F. Lupu

²Vascular Biology Laboratory, Thrombosis Research Institute, London, UK

,

L. Moons

³Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Leuven, Belgium

,

P. Carmeliet

³Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Leuven, Belgium

,

D. Goulding

²Vascular Biology Laboratory, Thrombosis Research Institute, London, UK

,

D. Collen

¹From the Center for Molecular and Vascular Biology, University of Leuven, Belgium

³Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Leuven, Belgium

› Author Affiliations

Abstract

Summary

Temporal and topographic expression of matrix metalloproteinases (MMPs) after perivascular electric injury was studied in wild-type (WT) and urokinase-deficient (u-PA^-/-) mice. Neointima formation after injury of the femoral artery was significantly reduced in u-PA^-/- mice as compared to WT mice (area of 0.002 ± 0.0007 mm² versus 0.008 ± 0.002 mm² at 3 weeks after injury; p <0.001), associated with impaired cellular migration (nuclear cell counts of 44 ± 5 versus 82 ± 9 in cross-sectional areas; p <0.001).

Zymographic and/or microscopic analysis indicated that MMP expression gradually increased to reach a maximum at 1 to 2 weeks after vascular injury. In general, MMP levels were lower in u-PA^-/- than in WT mice. In non-injured arteries, MMP-2 (gelatinase A) and MMP-3 (stromelysin-1) were produced mainly by adventitial fibroblasts and/or non-contractile smooth muscle cells (SMC). One week after injury, MMP-2 and MMP-3 levels were enhanced due to an increased number and size of producing cells; 2 to 3 weeks after injury, MMP-2 and MMP-3 were produced also by some contractile SMC, which stained with α-actin antiserum. MMP-9 (gelatinase B), MMP-12 (metalloelastase) and MMP-13 (collagenase-3) were found in macrophages located mainly in the adventitia. Immunogold electron microscopic examination revealed that MMP-2 was located predominantly in association with the cell surface of fibroblasts or SMC, while MMP-9 and MMP-12 were located in well defined storage granules within macrophages. MMP-2, MMP-3 and MMP-13, but not MMP-9 or MMP-12, were also found extracellularly, associated with elastin-containing structures (MMP-2), with the basement membrane and occasionally with collagen fibres (MMP-3), or with proteoglycans, collagen and elastin (MMP-13).

The temporal and topographic expression pattern of MMPs after vascular injury, coinciding with smooth muscle cell migration and neointima formation, thus is compatible with a role in vascular remodeling.

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References

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