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PMID: 1473813 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Gene expression in atherosclerotic lesions.

Herz ·Vol. 17 ·No. 5 ·1992-10-00 ·Pages 270-6

Ylä-Herttuala S

Abstract

Atherosclerotic lesions contain macrophages, smooth muscle cells and endothelial cells, all of which participate in lesion development. Upon stimulation these cells express a variety of different factors and receptors which are involved in lipid metabolism, cellular proliferation, tissue repair, immune response and inflammatory reactions. During the last few years, active expression of several genes has been reported in developing atherosclerotic lesions. These genes include scavenger receptor, 15-lipoxygenase, monocyte chemoattractant protein-1, macrophage colony stimulating factor-1, lipoprotein lipase, platelet-derived growth factor, tissue factor, apolipoprotein E, stromelysin, different adhesion molecules and various cytokines. Evidence continues to grow that the pattern of gene expression and the functional status of cells in different regions of atherosclerotic lesions may differ considerably and could be regulated by local factors present in atherosclerotic lesions. One such a powerful factor which may contribute to the regulation of gene expression in developing lesions is oxidized LDL which has been shown to affect the expression of cytokines, growth factors and chemotactic factors by arterial cells. Recent developments in the analysis of gene expression in the artery wall at the cellular level will undoubtedly increase our understanding about the sequence of events leading to the formation of atherosclerotic lesions.

MeSH Terms
Arteriosclerosis/genetics,physiopathology Cholesterol, LDL/blood Coronary Artery Disease/genetics,physiopathology Endothelium, Vascular/physiopathology Gene Expression Regulation/physiology Humans Lipid Peroxidation/genetics Muscle, Smooth, Vascular/physiopathology
Chemicals
Cholesterol, LDL
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Ylä-Herttuala S
Department of Biomedical Sciences, University of Tampere, Finland.
Article Info
Journal
Herz
Abbr.
Herz
ISSN
0340-9937
Published
1992-10-00
Pages
270-6
Language
English
Region
Germany
NLM ID
7801231
Subset
IM
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