Flint A P, Burton R D
J Endocrinol. 1984 Oct;103(1):31-42. doi: 10.1677/joe.0.1030031.
The cytosolic glucocorticoid receptor of ovine placental zona intima has been characterized and measured between day 51 of pregnancy and term, and levels compared with those in fetal lung. By ion-exchange and gel-filtration chromatography the molybdate-stabilized receptor was found to be an acidic molecule with Stokes radius approximately 8 nm; these physicochemical characteristics of the ovine placental receptor are comparable to those of receptors in glucocorticoid target tissues from nonruminants. Concentrations of cytosolic receptor in placenta (mean, 139 fmol/mg protein) were lower than those in fetal lung (627 fmol/mg) at all stages of gestation investigated. To some extent this difference was accounted for by a twofold higher concentration of protein in placental cytosols compared with those from fetal lung. In both tissues, cytosolic receptor concentrations were maximal between days 91 and 130, when fetal adrenal steroid secretion is low; receptor concentrations decreased before term. Fetal hypophysectomy, which resulted in prolonged gestation, raised receptor concentrations in placenta, but not in fetal lung. In both tissues, apparent dissociation constants for [3H]dexamethasone binding to glucocorticoid receptors were in the range 0.5-7.1 nmol/l; these dissociation constants did not change consistently between day 100 and term. In whole-cell preparations of placenta and fetal lung incubated in vitro there was time-dependent specific binding of [3H]dexamethasone by nuclei, and binding of labelled cytosolic receptor to isolated nuclei occurred at all stages of gestation investigated. Binding of [3H]dexamethasone by cytosolic receptor from placenta and fetal lung was inhibited by progesterone and 17 alpha-hydroxyprogesterone, as well as by cortisol, cortisone, 11-deoxycorticosterone and 11 beta-hydroxyprogesterone; 20 alpha-hydroxyprogesterone and 17 alpha,20 alpha-dihydroxypregn-4-en-3-one were less effective. In experiments to evaluate the possible antagonistic action of progesterone in whole-cell preparations, uptake of [3H]dexamethasone by nuclei was increased up to twofold in placental minces incubated with aminoglutethimide or epostane, when progesterone synthesis was reduced by 98 and 92 per cent respectively. Nuclear uptake in minces of fetal lung was blocked by concentrations of progesterone found in placenta. The existence of a placental glucocorticoid receptor confirms that fetal cortisol may act directly on the placenta to induce the enzymatic changes controlling the onset of labour.(ABSTRACT TRUNCATED AT 400 WORDS)
已对绵羊胎盘内膜的胞质糖皮质激素受体进行了鉴定,并在妊娠第51天至足月期间进行了测量,同时将其水平与胎儿肺中的水平进行了比较。通过离子交换和凝胶过滤色谱法发现,钼酸盐稳定的受体是一种酸性分子,斯托克斯半径约为8纳米;绵羊胎盘受体的这些物理化学特性与非反刍动物糖皮质激素靶组织中的受体相当。在所研究的妊娠各阶段,胎盘胞质受体浓度(平均139飞摩尔/毫克蛋白)均低于胎儿肺中的浓度(627飞摩尔/毫克)。在一定程度上,这种差异是由于胎盘胞质溶胶中的蛋白质浓度比胎儿肺中的高两倍。在这两种组织中,胞质受体浓度在第91天至130天之间最高,此时胎儿肾上腺类固醇分泌较低;足月前受体浓度下降。胎儿垂体切除导致妊娠期延长,使胎盘受体浓度升高,但胎儿肺中的受体浓度未升高。在这两种组织中,[3H]地塞米松与糖皮质激素受体结合的表观解离常数在0.5 - 7.1纳摩尔/升范围内;在第100天至足月期间,这些解离常数没有持续变化。在体外培养的胎盘和胎儿肺全细胞制剂中,细胞核对[3H]地塞米松有时间依赖性的特异性结合,并且在研究的妊娠各阶段,标记的胞质受体都能与分离的细胞核结合。胎盘和胎儿肺胞质受体对[3H]地塞米松的结合受到孕酮、17α-羟孕酮以及皮质醇、可的松、11-脱氧皮质酮和11β-羟孕酮的抑制;20α-羟孕酮和17α,20α-二羟基孕-4-烯-3-酮的抑制作用较弱。在评估孕酮在全细胞制剂中可能的拮抗作用的实验中,当孕酮合成分别减少98%和92%时,与氨鲁米特或依普斯坦一起孵育的胎盘碎块中,细胞核对[3H]地塞米松的摄取增加了两倍。胎盘内发现的孕酮浓度可阻断胎儿肺碎块中的细胞核摄取。胎盘糖皮质激素受体的存在证实胎儿皮质醇可能直接作用于胎盘,以诱导控制分娩开始的酶变化。(摘要截取自400字)