Vesey D A, Selden A C, Hodgson H J
Department of Medicine, Royal Postgraduate Medical School, London.
Gut. 1993 Nov;34(11):1601-6. doi: 10.1136/gut.34.11.1601.
This study investigated the mechanisms by which TAGH solution (a mixture of triiodothyronine, amino acids, glucagon, and heparin) induces DNA synthesis in hepatocytes in the liver of intact rats, with particular reference to events at the epidermal growth factor (EGF) receptor. Both partial hepatectomy and infusion of TAGH stimulated DNA synthesis at 24 hours and both procedures resulted in a reduction of EGF receptors assessed in plasma membranes isolated from rat liver at this time. In cell cultures, while EGF strongly stimulated DNA synthesis and started EGF receptor down regulation, TAGH had only a minor effect (1.5 x basal) on DNA synthesis and did not interact with or down regulate the EGF receptor. Membrane phosphorylation studies, however, showed that TAGH induced phosphorylation of tyrosine residues in the EGF receptor. The in vivo action of TAGH seems to entail recruitment of similar changes in the EGF receptor to those that occur after partial hepatectomy.
本研究调查了TAGH溶液(由三碘甲状腺原氨酸、氨基酸、胰高血糖素和肝素组成的混合物)在完整大鼠肝脏中诱导肝细胞DNA合成的机制,特别关注表皮生长因子(EGF)受体处发生的事件。部分肝切除术和TAGH输注均在24小时时刺激了DNA合成,且这两种操作均导致此时从大鼠肝脏分离的质膜中评估的EGF受体减少。在细胞培养中,虽然EGF强烈刺激DNA合成并启动EGF受体下调,但TAGH对DNA合成仅有轻微影响(为基础水平的1.5倍),且不与EGF受体相互作用或下调该受体。然而,膜磷酸化研究表明,TAGH诱导EGF受体中酪氨酸残基的磷酸化。TAGH的体内作用似乎需要在EGF受体中引发与部分肝切除术后发生的变化类似的改变。