T. Tanaka et al., Enhanced Fas/CD95-mediated apoptosis by epidermal growth factor in human endometrial epithelial cells, EUR J OB GY, 86(2), 1999, pp. 189-194
Citations number
39
Categorie Soggetti
Reproductive Medicine
Journal title
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
Epidermal growth factor (EGF) has been reported to regulate apoptosis in va
rious cell lineages. Throughout the menstrual cycle overexpression of the E
GF receptor in the secretory epithelium and constitutive expression of EGF
in all types of endometrial cells were identified by immunohistochemical st
udy of normal human endometrial tissues. However, it is not known whether E
GF also regulates endometrial apoptosis, This study examined the regulatory
functions of EGF in endometrial apoptosis by using a human endometrial epi
thelial cell line HHUA which is susceptible to Fas-mediated apoptosis. Alth
ough EGF alone did not affect the cell growth of HHUA, EGF pretreatment of
HHUA enhanced Fas-mediated growth suppression and Fas mediated DNA fragment
ation in the cells. Flowcytometric analyses demonstrated that EGF did not i
nduce Fas expression on the cell surface while expressions of the EGF recep
tor were down-regulated. These results suggest that EGF may enhance apoptot
ic susceptibility of the endometrial epithelium, especially in the secretor
y epithelium. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.