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低分子量甲状腺球蛋白导致一名12岁女孩出现甲状腺肿。

Low molecular weight thyroglobulin leading to a goiter in a 12-year-old girl.

作者信息

Silva J E, Santelices R, Kishihara M, Schneider A

出版信息

J Clin Endocrinol Metab. 1984 Mar;58(3):526-34. doi: 10.1210/jcem-58-3-526.

DOI:10.1210/jcem-58-3-526
PMID:6693549
Abstract

We characterized the abnormal thyroglobulin (TG) in the thyroid and serum of a 12-yr-old girl with a large sporadic multinodular goiter first noted at age 4 yr. She developed normally and had no clinical evidence of hypothyroidism. However, her serum T4 was less than 1.0 microgram/dl, T3 was 125 ng/dl, and TSH was 155 microU/ml. Serum PBI was 9.7 micrograms/dl, and more than 90% was not extractable with butanol. The 24-h radioactive iodine uptake was 55%, not dischargeable by perchlorate. Hormone formation was tested by the administration of 131I before surgery. [131I]T4 and [131I]T3, but not 131I-labeled iodotyrosines, were present in the thyroidal venous blood. Hydrolysis of 10,000 X g supernatants from three randomly obtained samples of the goiter revealed 66-77% of the 131I as iodotyrosines, 2-4% as iodothyronines, and 10-12% as undigestable material; the MIT to DIT ratio ranged from 3.1-8.7, and the T4 to T3 ratio ranged from 2.3-8.3. The TG level was 2.5 mg/g in the goiter and 9.4 micrograms/ml in the serum. The RIA displacement curves for the goiter and serum TG levels were both identical to the curve produced by normal human TG. The iodine contents of goiter and serum TG were 0.49% and 0.47% (wt/wt), respectively. The T4 to T3 ratio was lower in the goiter (approximately 5) than in the serum iodoprotein (approximately 45), whereas the calculation of the T4 to T3 ratio in the thyroidal secretion was less than 1. The goiter and serum TG bound normally to Concanavalin A, indicating that they contained carbohydrate. When either serum- or goiter-soluble proteins were gel-filtered (Bio-Gel A-5m), TG immunoreactivity and stable iodine elution profiles were the same, suggesting that no significant amounts of other iodoproteins were present in the thyroid or circulation. Both serum and goiter TG elution volumes corresponded to mol wt of approximately 9 X 10(4). A sedimentation rate of 10-11 S was found for both goiter and serum TG. An abnormally low mol wt of 8.5-9.0 X 10(4) was determined by sodium dodecyl sulfate-electrophoresis, in good agreement with the estimates from gel filtration studies. A single band was present on sodium dodecyl sulfate-electrophoresis regardless of whether the TG was reduced before the analysis. Thus, it is very unlikely that the low molecular weight was due to partial hydrolysis.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们对一名12岁女孩的甲状腺及血清中的异常甲状腺球蛋白(TG)进行了特征分析。该女孩4岁时首次发现患有散发性大结节性甲状腺肿,发育正常,无甲状腺功能减退的临床证据。然而,其血清T4低于1.0微克/分升,T3为125纳克/分升,促甲状腺激素(TSH)为155微单位/毫升。血清蛋白结合碘(PBI)为9.7微克/分升,其中90%以上不能被丁醇提取。24小时放射性碘摄取率为55%(高氯酸盐不能使其排出)。术前通过给予131I检测激素合成情况。甲状腺静脉血中存在[131I]T4和[131I]T3,但不存在131I标记的碘酪氨酸。对从甲状腺肿中随机获取的三个样本的10,000×g上清液进行水解后发现,131I中有66% - 77%为碘酪氨酸,2% - 4%为碘甲状腺原氨酸,10% - 12%为不可消化物质;一碘甲腺原氨酸(MIT)与二碘甲腺原氨酸(DIT)的比例为3.1 - 8.7,T4与T3的比例为2.3 - 8.3。甲状腺肿中TG水平为2.5毫克/克,血清中为9.4微克/毫升。甲状腺肿和血清TG水平的放射免疫分析(RIA)置换曲线均与正常人TG产生的曲线相同。甲状腺肿和血清TG的碘含量分别为0.49%和0.47%(重量/重量)。甲状腺肿中T4与T3的比例(约为5)低于血清碘蛋白中的比例(约为四十),而甲状腺分泌物中T4与T3比例的计算值小于1。甲状腺肿和血清TG与伴刀豆球蛋白A正常结合,表明它们含有碳水化合物。当对血清或甲状腺肿中的可溶性蛋白进行凝胶过滤(Bio - Gel A - 5m)时,TG免疫反应性和稳定碘洗脱曲线相同,这表明甲状腺或循环中不存在大量其他碘蛋白。血清和甲状腺肿TG的洗脱体积均对应于约9×10⁴的分子量。甲状腺肿和血清TG的沉降率均为10 - 11 S。通过十二烷基硫酸钠 - 电泳测定的异常低分子量为8.5 - 9.0×10⁴,与凝胶过滤研究的估计值高度一致。无论TG在分析前是否还原,十二烷基硫酸钠 - 电泳上均出现一条带。因此,分子量低极不可能是由于部分水解所致。(摘要截断于400字)

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Mild familial goitrous hypothyroidism associated with prolonged 131-iodine retention: possible defect in thyroglobulin synthesis.与131碘长时间潴留相关的轻度家族性甲状腺肿性甲状腺功能减退症:甲状腺球蛋白合成可能存在缺陷。
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Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure.导致先天性甲状腺肿的甲状腺球蛋白的定性和定量缺陷。甲状腺球蛋白(TG)基因结构中编码序列无明显基因缺失。
J Endocrinol Invest. 1989 Dec;12(11):805-13. doi: 10.1007/BF03350067.