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(American Journal of Pathology. 2006;168:340-348.)
© 2006 American Society for Investigative Pathology

Hepatocyte Growth Factor/Scatter Factor and MET Are Involved in Arterial Repair and Atherogenesis

Heather McKinnon*, Ermanno Gherardi{dagger}, Michael Reidy{ddagger} and David Bowyer*

From the Department of Pathology,* University of Cambridge, Cambridge, United Kingdom; the Medical Research Council Centre,{dagger} Cambridge, United Kingdom; and the Department of Pathology,{ddagger} University of Seattle, Seattle, Washington

Several studies have shown that in the arterial wall hepatocyte growth factor/scatter factor (HGF/SF) is expressed by smooth muscle cells (SMCs) but acts on endothelial cells, not SMCs. Other studies, however, have indicated that SMCs can respond to HGF/SF. We have reinvestigated expression and activity of HGF/SF and its receptor MET in arterial SMC and endothelial cell cultures and in whole arteries after superficial or deep injury or atherogenesis. High-density cultures of SMCs produced HGF/SF but did not express MET, whereas SMCs, at the leading edge of injured cultures, expressed both ligand and receptor and showed a dramatic motility and growth response to HGF/SF. In line with these results, HGF/SF and MET expression was undetectable in the media of uninjured carotid arteries but was induced after deep arterial injury in areas of SMC migration in the neointima. Strong MET expression was also observed in the SMCs of the atherosclerotic lesions of homozygous apoE–/– mice, whereas HGF/SF was expressed by macrophage-derived foam cells. These results demonstrate that MET is induced in migrating and proliferating SMCs and that HGF/SF and MET are key mediators of the SMC response in atherogenesis.






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Copyright © 2006 by the American Society for Investigative Pathology.