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hyt/hyt甲状腺功能减退小鼠的评估与特征分析。II.促甲状腺激素和甲状腺的异常情况。

Evaluation and characterization of the hyt/hyt hypothyroid mouse. II. Abnormalities of TSH and the thyroid gland.

作者信息

Stein S A, Shanklin D R, Krulich L, Roth M G, Chubb C M, Adams P M

机构信息

Department of Neurology, University of Texas Southwestern Medical Center, Dallas.

出版信息

Neuroendocrinology. 1989 May;49(5):509-19. doi: 10.1159/000125160.

Abstract

The hyt/hyt mouse (BALB/cBY-hyt, C.hytRF) provides a useful model for exploring the effect of inherited severe primary hypothyroidism. Studies were undertaken to try to define the basis of the primary hypothyroidism in mice homozygous for the autosomal recessive gene, hyt. These mice had congenital hypothyroidism of fetal onset after 15 days post conception. Through their lifetime, the hyt/hyt mice had reduced serum thyroxine (T4), triiodothyronine (T3), reduced thyroid gland intralumenal colloid on electron microscopy and a 100-fold elevation of TSH-like activity compared to hyt/+ littermates. Thyroglobulin made in hyt/hyt animals was similar in size to normal thyroglobulin which was inconsistent with a major structural thyroglobulin gene defect. The thyroglobulin was iodinated. Marked, erratic dilation of rough endoplasmic reticulum (RER) was noted in hyt/hyt mouse follicular cells. Despite these ultrastructural findings, pulse chase and immunoprecipitation studies with isolated hyt/hyt and normal thyroid glands indicated that normal thyroglobulin processing occurred in the RER and Golgi of the hyt/hyt mice. The hyt/hyt thyroid glands were hypoplastic compared to hyt/+ littermates. Histologically, the hyt/hyt thyroid glands demonstrated an increase in smaller follicular cells, and greater variability in follicular size compared to hyt/+ littermates. Histological and ultrastructural abnormalities in the gland were similar to those seen in certain cases of human congenital hypothyroidism with TSH receptor insensitivity of the thyroid gland. These findings along with the significant TSH elevation, the reduction in colloid and in serum T3 and T4, the efficacy of the hypothalamo-pituitary-thyroid feedback system, and previous observations of reduced iodine uptake and intrathyroidal T4, suggested that primary hypothyroidism in the hyt/hyt mouse might be due to a defect in TSH responsivity of the thyroid gland.

摘要

hyt/hyt小鼠(BALB/cBY-hyt,C.hytRF)为探索遗传性严重原发性甲状腺功能减退的影响提供了一个有用的模型。开展了多项研究,试图确定纯合常染色体隐性基因hyt小鼠原发性甲状腺功能减退的基础。这些小鼠在受孕后15天出现胎儿期先天性甲状腺功能减退。在其一生中,与hyt/+同窝小鼠相比,hyt/hyt小鼠血清甲状腺素(T4)、三碘甲状腺原氨酸(T3)降低,电子显微镜下甲状腺腺腔内胶体减少,促甲状腺激素(TSH)样活性升高100倍。hyt/hyt动物产生的甲状腺球蛋白大小与正常甲状腺球蛋白相似,这与甲状腺球蛋白主要结构基因缺陷不一致。甲状腺球蛋白被碘化。在hyt/hyt小鼠滤泡细胞中观察到粗面内质网(RER)明显且不规则的扩张。尽管有这些超微结构发现,但对分离的hyt/hyt和正常甲状腺进行的脉冲追踪和免疫沉淀研究表明,hyt/hyt小鼠的RER和高尔基体中发生了正常的甲状腺球蛋白加工。与hyt/+同窝小鼠相比,hyt/hyt甲状腺发育不全。组织学上,与hyt/+同窝小鼠相比,hyt/hyt甲状腺显示较小滤泡细胞增多,滤泡大小变异性更大。腺体的组织学和超微结构异常与某些人类先天性甲状腺功能减退且甲状腺对TSH不敏感的病例中所见相似。这些发现,连同显著的TSH升高、胶体以及血清T3和T4降低、下丘脑-垂体-甲状腺反馈系统的有效性,以及先前观察到的碘摄取和甲状腺内T4减少,提示hyt/hyt小鼠的原发性甲状腺功能减退可能是由于甲状腺对TSH反应性缺陷所致。

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