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Molecular aspects of thyroid hormone transporters, including MCT8, MCT10, and OATPs, and the effects of genetic variation in these transporters

机译:甲状腺激素转运蛋白(包括MCT8,MCT10和OATP)的分子方面,以及这些转运蛋白的遗传变异影响

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Thyroid hormone is a pleiotropic hormone with widespread biological actions. For instance, adequate levels of thyroid hormone are critical for the development of different tissues such as the central nervous system, but are also essential for the regulation of metabolic processes throughout life. The biological activity of thyroid hormone depends not only on serum thyroid hormone levels, but is also regulated at the tissue level by the expression and activity of deiodinases, which activate thyroid hormone or mediate its degradation. In addition, thyroid hormone transporters are necessary for the uptake of thyroid hormone into target tissues. With the discovery of monocarboxylate transporter 8 (MCT8) as a specific thyroid hormone transporter and the finding that mutations in this transporter lead to a syndrome of severe psychomotor retardation and elevated serum 3,3′,5-tri-iodothyronine levels known as the Allan–Herndon–Dudley syndrome, the interest in this area of research has greatly increased. In this review, we will focus on the molecular aspects of thyroid hormone transporters, including MCT8, MCT10, organic anion transporting polypeptides, and the effects of genetic variation in these transporters.
机译:甲状腺激素是具有广泛生物学作用的多效激素。例如,足够水平的甲状腺激素对于不同组织(如中枢神经系统)的发育至关重要,但对于整个生命的代谢过程调节也至关重要。甲状腺激素的生物学活性不仅取决于血清甲状腺激素水平,而且还受脱碘酶的表达和活性在组织水平的调节,脱碘酶激活甲状腺激素或介导其降解。另外,甲状腺激素转运蛋白对于将甲状腺激素摄取到靶组织中是必需的。随着发现单羧酸盐转运蛋白8(MCT8)作为一种特定的甲状腺激素转运蛋白,并且发现该转运蛋白的突变会导致严重的精神运动发育迟缓综合征和血清3,3',5-三碘甲状腺素水平升高,这被称为Allan –Herndon–Dudley综合征,对该领域的研究兴趣大大增加。在本文中,我们将重点研究甲状腺激素转运蛋白的分子方面,包括MCT8,MCT10,有机阴离子转运多肽,以及这些转运蛋白的遗传变异效应。

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