Schneider A B, Fleischmann K, Chu L
Biochim Biophys Acta. 1985 Mar 8;838(3):329-34. doi: 10.1016/0304-4165(85)90230-2.
In previous work we demonstrated that circulating thyroglobulin contains very little or no iodine. We have now characterized circulating thyroglobulin following administration of thyrotropin (TSH) to determine whether its iodine content remains low or increases after stimulation. The iodine content of circulating thyroglobulin was estimated from its density determined by equilibrium density gradient (isopycnic) centrifugation. TSH stimulated thyroglobulin from 182 +/- 28 ng/ml to 571 +/- 83 ng/ml at 8-14 h. Circulating thyroglobulin in the basal state had a density consistent with very little or no iodine. Its density increased following TSH to a maximum at 8-14 h which was nearly the same as the density of thyroglobulin extracted directly from the thyroid. To determine whether selective peripheral metabolism, based on the degree of iodination, could account for the density shift, purified rat thyroid thyroglobulin was injected into thyroidectomized rats. The density of thyroglobulin remained unchanged for 25 h during which time it was metabolized by more than 97%. Therefore, selective metabolism of thyroglobulin based on iodine content did not occur. We conclude that TSH causes a marked increase in the iodine content of circulating thyroglobulin. It is most likely that in the basal state circulating thyroglobulin comes from selective release of poorly iodinated molecules, while after TSH, it comes from release of previously synthesized, iodinated and stored molecules.
在之前的研究中,我们证明循环甲状腺球蛋白含碘极少或不含碘。我们现在对促甲状腺激素(TSH)给药后的循环甲状腺球蛋白进行了特性分析,以确定其碘含量在刺激后是保持较低水平还是增加。循环甲状腺球蛋白的碘含量通过平衡密度梯度(等密度)离心法测定的密度来估算。在8 - 14小时时,TSH将甲状腺球蛋白从182±28 ng/ml刺激至571±83 ng/ml。基础状态下的循环甲状腺球蛋白密度与极少或不含碘相符。TSH作用后其密度在8 - 14小时达到最大值,这几乎与直接从甲状腺提取的甲状腺球蛋白密度相同。为了确定基于碘化程度的选择性外周代谢是否能解释密度变化,将纯化的大鼠甲状腺甲状腺球蛋白注射到甲状腺切除的大鼠体内。甲状腺球蛋白的密度在25小时内保持不变,在此期间其代谢率超过97%。因此,基于碘含量的甲状腺球蛋白选择性代谢并未发生。我们得出结论,TSH导致循环甲状腺球蛋白的碘含量显著增加。很可能在基础状态下,循环甲状腺球蛋白来自碘化程度低的分子的选择性释放,而在TSH作用后,它来自先前合成、碘化并储存的分子的释放。