Bany B M, Zhang X, Kennedy T G
Department of Physiology, University of Western Ontario, London, Canada.
Biol Reprod. 1998 Jul;59(1):131-5. doi: 10.1095/biolreprod59.1.131.
Prostaglandin E2 (PGE2) increases decidualization and net plasminogen activator (PA) activity in the medium of cultured endometrial stromal cells from ovariectomized rats sensitized for the decidual cell reaction. Because interleukin-1alpha (IL-1alpha) and epidermal growth factor (EGF) stimulate PGE2 production by these cells, the present study determined their effects on decidualization and on the levels of PA activity in the medium. Cells were treated with or without IL-1alpha (20 ng/ml) and EGF (40 ng/ml) for up to 72 h, and net PA activity in the medium and alkaline phosphatase (ALP) activity (a marker for decidualization) in the cells were measured. After 48 and 72 h of treatment with IL-1alpha, net PA activity levels decreased by 60% and 85%, respectively. EGF significantly increased net PA activity at 24, 48, and 72 h. ALP activity in the cells at 24, 48, and 72 h increased in response to IL-1alpha but not EGF. These results indicate that IL-1alpha, but not EGF, enhances decidualization of the cells as indicated by ALP activity. Moreover, they suggest that net PA activity in the medium is not a useful marker of decidualization.
前列腺素E2(PGE2)可增强去卵巢大鼠子宫内膜基质细胞培养基中的蜕膜化作用及纤溶酶原激活物(PA)净活性,这些大鼠已对蜕膜细胞反应致敏。由于白细胞介素-1α(IL-1α)和表皮生长因子(EGF)可刺激这些细胞产生PGE2,因此本研究确定了它们对蜕膜化及培养基中PA活性水平的影响。用或不用IL-1α(20 ng/ml)和EGF(40 ng/ml)处理细胞长达72小时,并测量培养基中的PA净活性以及细胞中的碱性磷酸酶(ALP)活性(蜕膜化的标志物)。用IL-1α处理48小时和72小时后,PA净活性水平分别下降了60%和85%。EGF在24小时、48小时和72小时时显著增加了PA净活性。IL-1α可使细胞在24小时、48小时和72小时时的ALP活性增加,而EGF则无此作用。这些结果表明,如ALP活性所示,IL-1α而非EGF可增强细胞的蜕膜化作用。此外,它们提示培养基中的PA净活性并非蜕膜化的有用标志物。