Oberleithner H
Nanolab, Institute of Physiology II, University Münster, D-48149, Münster, Germany,
J Membr Biol. 2004 Jun 1;199(3):127-34. doi: 10.1007/s00232-004-0685-8.
Signalling between cytosol and nucleus is mediated by nuclear pores. These supramolecular complexes represent intelligent nanomachines regulated by a wide spectrum of factors. Among them, steroid hormones specifically interact with the pores and thus modify ion conductivity and macromolecule permeability of the nuclear envelope. In response to aldosterone the pores undergo dramatic changes in conformation, changes that depend on the nature of the transported cargo. Such changes can be imaged at the nanometer scale by using atomic force microscopy. Furthermore, steroid-induced macromolecule transport across the nuclear envelope causes osmotic water movements and nuclear swelling. Drugs that interact with intracellular steroid receptors (spironolactone) or with plasma membrane sodium channels (amiloride) inhibit swelling. Steroid hormone action is blocked when nuclear volume changes are prevented. This is shown in frog oocytes and human endothelial cells. In conclusion, nuclear pores serve as steroid-sensitive gates that determine nuclear activity.
细胞质和细胞核之间的信号传导由核孔介导。这些超分子复合物代表了受多种因素调节的智能纳米机器。其中,类固醇激素与核孔特异性相互作用,从而改变核膜的离子传导性和大分子通透性。在醛固酮的作用下,核孔的构象会发生显著变化,并取决于所转运货物的性质。通过原子力显微镜可以在纳米尺度上对这些变化进行成像。此外,类固醇诱导的大分子穿过核膜的转运导致渗透性水运动和核肿胀。与细胞内类固醇受体相互作用的药物(螺内酯)或与质膜钠通道相互作用的药物(氨氯地平)可抑制肿胀。当核体积变化被阻止时,类固醇激素的作用就会被阻断。这在蛙卵母细胞和人内皮细胞中得到了证实。总之,核孔作为类固醇敏感的闸门决定了核活性。