Mol J A, Krenning E P, Docter R, Rozing J, Hennemann G
J Biol Chem. 1986 Jun 15;261(17):7640-3.
The role of the rat liver plasma membrane in the regulation of uptake and subsequent deiodination of thyroxine (T4) or the biologically active thyroid hormone 3,3',5-triiodothyronine (T3) was investigated. Here we report on the production of monoclonal antibodies raised against rat hepatocytes. Two antibodies were selected. Antibody ER-22 did bind to a Mr 52,000 membrane protein and inhibited the 1- and 5-min uptake of both T4 and T3 by primary cultured rat hepatocytes in a dose-dependent fashion. As the uptake of T4 and T3 depends on the presence of a sodium gradient over the plasma membrane, the inhibitory potency of ER-22 on the Na+,K+-ATPase activity was investigated. No inhibition of the uptake of 86Rb+ could be determined, indicating that antibody ER-22 is not directed against the Na+,K+-ATPase but probably the carrier protein itself. Clearance of T3 from the medium and concomitant iodide production by cultured rat hepatocytes during a 20-h incubation in the presence of ER-22 were both inhibited by 50% with respect to a control incubation in the absence of monoclonal antibody, pointing to the importance of carrier-mediated transport in cellular uptake and metabolism of T3. A second monoclonal antibody did bind to two other plasma membrane proteins but did not inhibit transport of thyroid hormone.
研究了大鼠肝细胞膜在调节甲状腺素(T4)或生物活性甲状腺激素3,3',5-三碘甲状腺原氨酸(T3)摄取及随后的脱碘过程中的作用。在此,我们报告针对大鼠肝细胞产生的单克隆抗体。筛选出两种抗体。抗体ER-22确实能与一种分子量为52,000的膜蛋白结合,并以剂量依赖方式抑制原代培养的大鼠肝细胞对T4和T3的1分钟及5分钟摄取。由于T4和T3的摄取依赖于质膜上钠梯度的存在,因此研究了ER-22对Na+,K+-ATP酶活性的抑制效力。未检测到对86Rb+摄取的抑制作用,表明抗体ER-22并非针对Na+,K+-ATP酶,而可能针对载体蛋白本身。在存在ER-22的情况下,培养的大鼠肝细胞在20小时孵育期间,T3从培养基中的清除以及伴随的碘产生相对于无单克隆抗体的对照孵育均被抑制了50%,这表明载体介导的转运在细胞摄取和T3代谢中具有重要作用。第二种单克隆抗体确实能与另外两种质膜蛋白结合,但不抑制甲状腺激素的转运。