Mohan A, Asselin J, Sargent I L, Groome N P, Muttukrishna S
Nuffield Department of Obstetrics and Gynaecology, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK.
Eur J Endocrinol. 2001 Oct;145(4):505-11. doi: 10.1530/eje.0.1450505.
Maternal serum inhibin A and activin A are higher in pre-eclampsia than in normal pregnancy. The placenta is a source of these proteins in pregnancy. The aim of this study was to investigate the effect of growth factors and proinflammatory cytokines that are raised in pre-eclampsia on the secretion of dimeric inhibin A, activin A and follistatin by villous cytotrophoblasts in culture.
Villous cytotrophoblasts were prepared from term placentae and cultured in serum-free media. Cells were treated with increasing concentrations of tumour necrosis factor (TNF)-alpha, interleukin (IL)-1beta, transforming growth factor (TGF)-beta1, granulocyte and monocyte colony-stimulating factor (GMCSF), inhibin A, activin A and follistatin for 2 days. Culture supernatants were assayed for human chorionic gonadotrophin (hCG), inhibin A, activin A and follistatin as appropriate. Experiments were repeated at least three times with each cytokine or growth factor and the data pooled.
Cytotrophoblasts syncytialise and spontaneously secrete hCG, inhibin A and activin A in culture. Follistatin levels were <20 pg/ml in most experiments. Activin A secretion was increased in culture in a dose-dependent manner by IL-1beta (approximately 150%, P<0.05), TNF-alpha (approximately 35%, P=0.02) and GMCSF (approximately 100%, P<0.01). hCG secretion was inhibited in a dose-dependent manner by TNF-alpha (50%, P<0.05). Inhibin A was stimulated by IL-1beta ( approximately 30%, P=0.05). Inhibin A, activin A, follistatin or TGF-beta1 did not have a significant effect on any measured parameters.
These data show that inflammatory cytokines increase the secretion of activin A by trophoblasts in culture. The presence of very low levels, or no follistatin (<20 pg/ml) in the culture media suggests 'free' activin A could have autocrine/paracrine effects on cytotrophoblasts. Inhibin A secretion was stimulated by IL-1beta. However, absence of an effect by the other cytokines investigated on inhibin A in this study suggests that the mechanism(s) involved in increasing maternal circulating levels of inhibin A and activin A in pre-eclampsia are controlled differentially.
子痫前期孕妇血清抑制素A和激活素A水平高于正常妊娠。胎盘是孕期这些蛋白质的来源之一。本研究旨在探讨子痫前期中升高的生长因子和促炎细胞因子对培养的绒毛细胞滋养层细胞分泌二聚体抑制素A、激活素A和卵泡抑素的影响。
从足月胎盘制备绒毛细胞滋养层细胞,并在无血清培养基中培养。用浓度递增的肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、转化生长因子(TGF)-β1、粒细胞和单核细胞集落刺激因子(GMCSF)、抑制素A、激活素A和卵泡抑素处理细胞2天。视情况检测培养上清液中的人绒毛膜促性腺激素(hCG)、抑制素A、激活素A和卵泡抑素。每种细胞因子或生长因子的实验至少重复三次,并汇总数据。
细胞滋养层细胞在培养中会融合并自发分泌hCG、抑制素A和激活素A。在大多数实验中,卵泡抑素水平<20 pg/ml。激活素A的分泌在培养中因IL-1β(约150%,P<0.05)、TNF-α(约35%,P=0.02)和GMCSF(约100%,P<0.01)呈剂量依赖性增加。TNF-α以剂量依赖性方式抑制hCG分泌(50%,P<0.05)。IL-1β刺激抑制素A分泌(约30%,P=0.05)。抑制素A、激活素A、卵泡抑素或TGF-β1对任何测量参数均无显著影响。
这些数据表明,炎性细胞因子可增加培养的滋养层细胞中激活素A的分泌。培养基中卵泡抑素水平极低或不存在(<20 pg/ml)表明“游离”激活素A可能对细胞滋养层细胞有自分泌/旁分泌作用。IL-1β刺激抑制素A分泌。然而,本研究中所研究的其他细胞因子对抑制素A无作用,这表明子痫前期孕妇循环中抑制素A和激活素A水平升高的机制受到不同的调控。