Welshons W V, Lieberman M E, Gorski J
Nature. 1984;307(5953):747-9. doi: 10.1038/307747a0.
According to the current model of steroid hormone action oestrogen is thought to bind to its receptor in the cytoplasm of target cells and the oestrogen-receptor complex is then translocated into the nucleus. This model is based on evidence obtained in homogenized cell preparations in which free receptor is associated with the cytosol, whereas steroid-bound receptor is associated with the nuclear fraction. Some data suggest, however, that the unfilled receptor may reside in the nucleus, and that cytosolic localization represents an extraction artefact. We have now reinvestigated the subcellular distribution of unfilled oestrogen receptor using cytochalasin B-induced enucleation to obtain cytoplast and nucleoplast fractions from receptor-containing GH3 cells derived from rat pituitary tumours. We found that cytoplasts prepared from GH3 cells contain little oestrogen-binding activity and that most of the unfilled oestrogen receptors are associated with the nuclear fraction. We therefore suggest that the standard model is in error and that the unoccupied receptor is nuclear in the intact cell.
根据当前的类固醇激素作用模型,雌激素被认为与靶细胞胞质中的受体结合,然后雌激素-受体复合物转移到细胞核中。该模型基于在匀浆细胞制剂中获得的证据,其中游离受体与胞质溶胶相关,而类固醇结合受体与核部分相关。然而,一些数据表明,未结合的受体可能存在于细胞核中,而胞质定位代表一种提取假象。我们现在使用细胞松弛素B诱导去核,从源自大鼠垂体肿瘤的含受体GH3细胞中获得细胞质体和核质体部分,重新研究了未结合雌激素受体的亚细胞分布。我们发现,从GH3细胞制备的细胞质体几乎没有雌激素结合活性,并且大多数未结合的雌激素受体与核部分相关。因此,我们认为标准模型是错误的,在完整细胞中未占据的受体位于细胞核中。