Abstract:
:Progressive pathophysiologic modifications of endothelial cells are associated with aging. In vitro, endothelial cell senescence is accompanied by the failure to proliferate as well as by perturbations in gene expression. Here we show that (i) senescence enhances monoblastoid U937 cell adhesion to the endothelial monolayer; (ii) the enhanced interaction between senescent endothelial cells and U937 cells is mediated, at least in part, by the overexpression of ICAM-1; and (iii) LPS and interleukin 1 alpha, but not tumor necrosis factor alpha, are unable to stimulate the adhesion of U937 to senescent endothelial cells. Since monocyte adhesion to the endothelium is an early event in atherosclerosis, the altered adhesive properties observed in senescent cells could give insights into the formation of atherosclerotic lesions.
journal_name
Exp Cell Resjournal_title
Experimental cell researchauthors
Maier JA,Statuto M,Ragnotti Gdoi
10.1006/excr.1993.1246subject
Has Abstractpub_date
1993-09-01 00:00:00pages
270-4issue
1eissn
0014-4827issn
1090-2422pii
S0014-4827(83)71246-2journal_volume
208pub_type
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