Gerber H, Studer H, von Grünigen C
Endocrinology. 1985 Jan;116(1):303-10. doi: 10.1210/endo-116-1-303.
Autoradiographs of human goiters demonstrate that the speed of diffusion of newly iodinated thyroglobulin (Tgb) molecules through the colloid space may vary widely from one follicle to another. Since the mechanisms which govern the mixing of the colloid are unknown, we investigated the effect of TSH on these processes in rat thyroid glands. Autoradiographs were prepared from thyroids of rats killed 1 h after 125I or 4 h after [3H]leucine injection. In animals treated with T4 for 2 days, 70% of all follicles showed ring labeling of the colloid periphery with both isotopes, indicating slow mixing of newly synthesized and newly iodinated Tgb molecules with preexisting ones. TSH markedly enhanced the mixing process, thereby diminishing the incidence of ring reactions to roughly 10% of all follicles. These results were expected. Unexpected however, was, the nearly total absence of rings in thyroids treated with T4 for 25 days. Semiquantitative autoradiography revealed a higher absolute number of both newly iodinated and newly synthesized Tgb molecules in the core of follicles in chronically suppressed compared to acutely suppressed thyroids. Moreover, after chronic T4 pretreatment, the effect of TSH on diffusion was the opposite of that observed in acutely T4-treated glands, since 0.5 IU TSH injected twice daily between days 21 and 25 caused the reappearance of 125I and [3H]leucine labeled rings in 44% and 33%, respectively, of all follicles. We conclude that acute TSH suppression slows intraluminal diffusion of thyroglobulin molecules and acute TSH injection accelerates the mixing process, whereas, in contrast, chronic TSH suppression improves and acute TSH action on chronically suppressed follicles impairs diffusion. Therefore, the impact of TSH-mediated processes on the hydrodynamic properties of colloid, and thereby on the intraluminal iodination and coupling process, is more complex than hitherto thought.
人体甲状腺肿的放射自显影片显示,新碘化的甲状腺球蛋白(Tgb)分子在胶体间隙中的扩散速度在不同滤泡之间可能有很大差异。由于控制胶体混合的机制尚不清楚,我们研究了促甲状腺激素(TSH)对大鼠甲状腺这些过程的影响。在注射125I后1小时或[3H]亮氨酸后4小时处死大鼠,取其甲状腺制作放射自显影片。在用T4处理2天的动物中,70%的滤泡显示两种同位素均在胶体周边呈环状标记,表明新合成和新碘化的Tgb分子与预先存在的分子混合缓慢。TSH显著增强了混合过程,从而使环状反应的发生率降至所有滤泡的约10%。这些结果在意料之中。然而,出乎意料的是,在用T4处理25天的甲状腺中几乎完全没有环状结构。半定量放射自显影显示,与急性抑制的甲状腺相比,长期抑制的甲状腺滤泡核心中新碘化和新合成的Tgb分子的绝对数量更高。此外,在长期T4预处理后,TSH对扩散的影响与急性T4处理的腺体中观察到的相反,因为在第21天至25天之间每天注射两次0.5 IU TSH,分别导致44%和33%的所有滤泡中出现125I和[3H]亮氨酸标记的环状结构。我们得出结论,急性TSH抑制会减缓甲状腺球蛋白分子在管腔内的扩散,急性注射TSH会加速混合过程,而相比之下,慢性TSH抑制会改善,急性TSH对长期抑制的滤泡的作用会损害扩散。因此,TSH介导的过程对胶体流体动力学性质的影响,进而对管腔内碘化和偶联过程的影响,比迄今认为的更为复杂。