Reports |
From Molecular Cardiology, Department of Internal Medicine IV, University of Frankfurt, Germany.
Correspondence to Stefanie Dimmeler, PhD, Molecular Cardiology, University of Frankfurt, Theodor Stern-Kai 7, 60590 Frankfurt, Germany. E-mail Dimmeler@em.uni-frankfurt.de
Key Words: nitric oxide aging endothelial cells telomerase
| Introduction |
|---|
The incidence of atherosclerosis increases with age. Aging is associated not only with endothelial dysfunction, a key pathogenic factor in atherosclerotic disease progression,1 2 but also impairs angiogenesis,3 suggesting that the process of aging itself affects endothelial cell (EC) function.
On a cellular level, aging leads to an irreversible state of cell cycle
arrest known as replicative senescence.4 It is generally
believed that a relevant factor in regulating cellular life span is the
telomere length.5 Telomerase, a ribonucleoprotein with
reverse transcriptase activity, synthesizes
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