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促甲状腺激素受体及其在格雷夫斯病中的作用。

Thyroid-stimulating hormone receptor and its role in Graves' disease.

作者信息

Chistiakov D A

机构信息

Laboratory of Aquatic Ecology, Katholieke Universiteit Leuven, B-3000, Leuven, Belgium.

出版信息

Mol Genet Metab. 2003 Dec;80(4):377-88. doi: 10.1016/j.ymgme.2003.09.001.

Abstract

The thyroid-stimulating hormone (TSH, or thyrotropin) receptor (TSHR) mediates the activating action of TSH to the thyroid gland, resulting in the growth and proliferation of thyrocytes and thyroid hormone production. In Graves' disease, thyroid-stimulating autoantibodies can mimic TSH action and stimulate thyroid cells. This leads to hyperthyroidism and abnormal overproduction of thyroid hormone. TSHR-antibodies-binding epitopes on the receptor molecule are well studied. Mechanism of TSHR-autoantibodies production is more or less clear but a susceptibility gene, which is linked to their production, is still unknown. Genetic studies show no linkage between the TSHR gene and Graves' disease. Among three common polymorphisms in the TSHR gene, only the D727E germline polymorphism in the cytoplasmic tail of the receptor showed an association with the disease, and this association is weak. The absence of a strong genetic effect of the TSHR polymorphisms in such a common and complex disorder as Graves' disease may be explained by a high degree of evolutionary conservation in TSHR. This can be shown by naturally existing germline and somatic mutations in the TSHR gene that cause various types of nonautoimmune and hereditary thyroid disease.

摘要

促甲状腺激素(TSH,或促甲状腺素)受体(TSHR)介导TSH对甲状腺的激活作用,导致甲状腺细胞生长、增殖以及甲状腺激素的产生。在格雷夫斯病中,促甲状腺自身抗体可模拟TSH的作用并刺激甲状腺细胞。这会导致甲状腺功能亢进以及甲状腺激素异常过量产生。受体分子上TSHR抗体结合表位已得到充分研究。TSHR自身抗体产生的机制或多或少已较为明确,但与其产生相关的易感基因仍不明确。遗传学研究表明TSHR基因与格雷夫斯病之间不存在连锁关系。在TSHR基因的三种常见多态性中,只有受体胞质尾区的D727E种系多态性与该病存在关联,且这种关联较弱。在格雷夫斯病这种常见且复杂的疾病中,TSHR多态性缺乏强烈的遗传效应,这可能是由于TSHR具有高度的进化保守性。TSHR基因中自然存在的种系和体细胞突变可导致各种类型的非自身免疫性和遗传性甲状腺疾病,这一点即可证明。

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