Aprison B S, Martin-Morris L, Spolski R J, Wangh L J
In Vitro Cell Dev Biol. 1986 Aug;22(8):457-64. doi: 10.1007/BF02623446.
We have recently shown that extensive proliferation of liver parenchymal cells takes place in adult male Xenopus frogs in response to estradiol-17 beta, which also induces synthesis and secretion of vitellogenin, the precursor of yolk proteins. We demonstrate here that liver parenchymal cells from adult male animals can be maintained for several weeks in a defined tissue culture medium containing added insulin, dexamethasone, and triiodothyronine. Under these conditions the cells do not divide, but can synthesize DNA. Maximum DNA synthesis occurs in cells that have achieved monolayer morphology under low plating densities. Estradiol-17 beta causes a dose-dependent increase in the number of cells synthesizing DNA, as well as inducing synthesis of vitellogenin. Estrogen-dependent, but not background, DNA synthesis is inhibited by the antiestrogen tamoxifen. These results imply that estradiol-17 beta acts directly on liver cells to initiate DNA replication, probably by interaction with a receptor protein and induction of specific gene transcription.
我们最近发现,成年雄性非洲爪蟾的肝实质细胞会因17β-雌二醇而大量增殖,17β-雌二醇还能诱导卵黄蛋白原(卵黄蛋白的前体)的合成与分泌。我们在此证明,成年雄性动物的肝实质细胞能在添加了胰岛素、地塞米松和三碘甲状腺原氨酸的特定组织培养基中维持数周。在这些条件下,细胞不分裂,但能合成DNA。最大程度的DNA合成发生在低密度接种下已形成单层形态的细胞中。17β-雌二醇会使合成DNA的细胞数量呈剂量依赖性增加,同时诱导卵黄蛋白原的合成。抗雌激素他莫昔芬可抑制雌激素依赖性而非背景性的DNA合成。这些结果表明,17β-雌二醇可能通过与受体蛋白相互作用并诱导特定基因转录,直接作用于肝细胞以启动DNA复制。