4.5 Article

Effects of estrogen, progesterone, and combination exposure on interleukin-1β-induced expression of VCAM-1, ICAM-1, PECAM, and E-selectin by human female iliac artery endothelial cells

Journal

JOURNAL OF SURGICAL RESEARCH
Volume 105, Issue 2, Pages 215-219

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1006/jsre.2002.6405

Keywords

-

Categories

Ask authors/readers for more resources

The cardioprotective effect of hormone replacement therapy (HRT) in healthy, postmenopausal women is well documented. Little work has been performed on the effect of HRT in peripheral arteries. Recent work suggests that HRT may adversely affect the patency of peripheral grafts. This study investigates the in vitro effects of estrogen and/or progesterone exposure on adhesion molecule expression by normal human female iliac artery endothelial cells (HIAEC). Control and interleukin-1beta (IL-1beta)-stimulated HIAEC monolayers were labeled with fluorescent-tagged antibodies against the adhesion molecules VCAM-1, ICAM-1, PECAM, and E-selectin. FACS analysis was used to measure antibody-labeled adhesion molecule expression. ICAM-1 and PECAM were found to be constitutively expressed. VCAM-1 and ICAM-1 expression were significantly upregulated by IL-1beta, while E-selectin was neither constitutively expressed nor upregulated by IL-1beta. Pretreatment with estrogen or progesterone alone decreased IL-1beta-stimulated VCAM-1 and ICAM-1 expression, but not to statistically significant levels. Combined hormone exposure significantly decrease in an additive fashion, the expression of VCAM-1 an ICAM-1 in stimulated cells. This study supports extension of the beneficial effects ascribed to HRT to include the peripheral arterial endothelium of healthy women. (C) 2002 Elsevier Science (USA).

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available