Benathan M, Lemarchand-Béraud T, Gautier A, Gardiol D
Virchows Arch B Cell Pathol Incl Mol Pathol. 1983;44(3):323-36. doi: 10.1007/BF02890181.
Gunn rats have a marked deficiency in hepatic UDP-glucuronosyl transferase activity which results in hyperthyroxinemia and hyperbilirubinemia. Their thyroids show a brownish-black discoloration associated ultrastructurally with intracellular dense granules and intraluminal dense masses. In order to determine whether colloid composition and colloid proteolysis are altered in the thyroid of the Gunn rat compared with the Wistar rat, we studied the in situ resistance of thyroid proteins to in vitro proteolysis, the pattern of in vivo (125I) labeled thyroid iodoproteins and the proteolysis of isolated iodoprotein fractions in both strains of rats. For the cytochemical study, thin sections of aldehyde-fixed and plastic-embedded thyroid tissue were treated with 0.3 or 1% pronase in aqueous solution. With the low concentration of pronase, the secretory granules in C-cells and the apical vesicles in follicular cells were extensively digested in both strains of rats, whereas the colloid in the follicular lumen and the colloid droplets were only partially digested. With the high concentration of pronase, the colloid in the lumen and the colloid droplets were more markedly digested in both strains. In the presence of both concentrations of pronase, the dense granules and intraluminal dense masses were unchanged in the Gunn rats. The (125I) iodoprotein pattern was investigated 24 h after a single injection of (125I) iodide and by labeling at the isotopic equilibrium. It was found that the (125I) thyroglobulin fraction was reduced, whereas the (125I) 3-8 S fraction was increased in Gunn rats compared to Wistar rats. Pronase hydrolysis of the soluble (125I) iodine fraction showed similar pronase-resistant fractions in both strains with the single labeling procedure. At the isotopic equilibrium, the pronase resistant fraction was significantly increased in Gunn rats (Gunn 24.0 +/- 5.3%; Wistar: 13.7 +/- 3.1% of the soluble 125I) and a linear correlation was observed between the (125I) 3-8 S fraction of the soluble extract and the pronase-resistant fraction. These data suggest that iodocompounds of small molecular size and low turnover accumulate in the thyroid of the Gunn rat due to their strong resistance to in vivo hydrolysis. A local accumulation of 3-8 S iodocompounds may occur within the intracellular dense granules and intraluminal dense masses in the thyroid of Gunn rat.
冈恩大鼠肝脏中的尿苷二磷酸葡糖醛酸基转移酶活性明显缺乏,这导致了高甲状腺素血症和高胆红素血症。它们的甲状腺呈现出棕黑色变色,在超微结构上与细胞内致密颗粒和管腔内致密团块有关。为了确定与Wistar大鼠相比,冈恩大鼠甲状腺中的胶体成分和胶体蛋白水解是否发生改变,我们研究了两种品系大鼠甲状腺蛋白对体外蛋白水解的原位抗性、体内(125I)标记的甲状腺碘蛋白模式以及分离的碘蛋白组分的蛋白水解情况。对于细胞化学研究,醛固定和塑料包埋的甲状腺组织薄片用0.3%或1%的链霉蛋白酶水溶液处理。在链霉蛋白酶浓度较低时,两种品系大鼠的C细胞分泌颗粒和滤泡细胞顶端小泡均被大量消化,而滤泡腔内的胶体和胶体小滴仅被部分消化。在链霉蛋白酶浓度较高时,两种品系大鼠管腔内的胶体和胶体小滴被更明显地消化。在两种链霉蛋白酶浓度下,冈恩大鼠的致密颗粒和管腔内致密团块均未改变。在单次注射(125I)碘化物24小时后并在同位素平衡时进行标记,研究了(125I)碘蛋白模式。结果发现,与Wistar大鼠相比,冈恩大鼠的(125I)甲状腺球蛋白组分减少,而(125I)3 - 8 S组分增加。在单次标记过程中,两种品系大鼠中可溶性(125I)碘组分的链霉蛋白酶水解显示出相似的抗链霉蛋白酶组分。在同位素平衡时,冈恩大鼠中抗链霉蛋白酶组分显著增加(冈恩大鼠:可溶性125I的24.0 +/- 5.3%;Wistar大鼠:13.7 +/- 3.1%),并且在可溶性提取物的(125I)3 - 8 S组分与抗链霉蛋白酶组分之间观察到线性相关性。这些数据表明,由于对体内水解具有较强抗性,小分子大小和低周转率的碘化合物在冈恩大鼠的甲状腺中积累。在冈恩大鼠甲状腺的细胞内致密颗粒和管腔内致密团块中可能会发生3 - 8 S碘化合物的局部积累。