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Circulation. 2000;101:1799-1805

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Right arrow Smooth muscle proliferation and differentiation

(Circulation. 2000;101:1799.)
© 2000 American Heart Association, Inc.


Clinical Investigation and Reports

Enzymatically Degraded, Nonoxidized LDL Induces Human Vascular Smooth Muscle Cell Activation, Foam Cell Transformation, and Proliferation

Mariam Klouche, MD; Stefan Rose-John, PhD; Walther Schmiedt, MD; Sucharit Bhakdi, MD

From the Institute of Medical Microbiology (M.K., S.B.), Department of Internal Medicine (S.R.-J.), Section of Pathophysiology and Department of Heart and Thoracic Surgery (W.S.), University of Mainz, Germany.

Correspondence to Dr Mariam Klouche, Institute of Medical Microbiology, University of Mainz, Hochhaus am Augustusplatz, 55101 Mainz, Germany. E-mail: klouche{at}mail.uni-mainz.de

Background—Enzymatic, nonoxidative modification transforms LDL to an atherogenic molecule (E-LDL) that activates complement and macrophages and is present in early atherosclerotic lesions.

Methods and Results—We report on the atherogenic effects of E-LDL on human vascular smooth muscle cells (SMC). E-LDL accumulated in these cells, and this was accompanied by selective induction of monocyte chemotactic protein-1 in the absence of effects on the expression of interleukin (IL)-8, RANTES, or monocyte inflammatory proteins-1{alpha} and -ß). Furthermore, E-LDL stimulated the expression of gp130, the signal-transducing chain of the IL-6 receptor (IL-6R) family, and the secretion of IL-6. E-LDL invoked mitogenic effects on SMC through 2 mechanisms. First, an autocrine mitogenic circuit involving platelet-derived growth factor and fibroblast growth factor-ß was induced. Second, upregulation of gp130 rendered SMC sensitive to transsignaling through the IL-6/sIL-6R activation pathway. Because E-LDL promoted release of both IL-6 and sIL-6R from macrophages, application of macrophage cell supernatants to prestimulated SMC provoked a pronounced and sustained proliferation of the cells.

Conclusions—E-LDL can invoke alterations in SMC that are characteristic of the evolving atherosclerotic lesion.


Key Words: atherosclerosis • lipoproteins • cells • muscle, smooth • enzymes




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