Department of Anatomy and Physiology, Kansas State University College of Veterinary Medicine, Manhattan, KS 66506, USA.
J Physiol. 2011 Dec 15;589(Pt 24):5929-39. doi: 10.1113/jphysiol.2011.218594. Epub 2011 Oct 10.
The thyroid hormones thyroxine (T(4)) and triiodothyronine (T(3)) play key roles in regulating development, growth and metabolism in pre- and postnatal life. Iodide (I(-)) is an essential component of the thyroid hormones and is accumulated avidly by the thyroid gland. The rarity of elemental iodine and I(-) in the environment challenges the thyroid to orchestrate a remarkable series of transport processes that ultimately ensure sufficient levels for hormone synthesis. In addition to actively extracting circulating I(-), thyroid follicular epithelial cells must also translocate I(-) into a central intrafollicular compartment, where thyroglobulin is iodinated to form the protein precursor to T(4) and T(3). In the last decade, several bodies of evidence render questionable the notion that I(-) exits thyrocytes solely via the Cl(-)/I(-) exchanger Pendrin (SLC26A4), therefore necessitating reconsideration of several other candidate I(-) conduits: the Cl(-)/H(+) antiporter, CLC-5, the cystic fibrosis transmembrane conductance regulator (CFTR) and the sodium monocarboxylic acid transporter (SMCT1).
甲状腺激素甲状腺素(T4)和三碘甲状腺原氨酸(T3)在胎儿期和出生后的发育、生长和代谢中发挥着关键作用。碘(I-)是甲状腺激素的重要组成部分,甲状腺会强烈地积累碘。环境中元素碘和 I-的稀有性挑战了甲状腺,使其协调一系列非凡的运输过程,最终确保有足够的水平用于激素合成。除了主动提取循环中的 I-之外,甲状腺滤泡上皮细胞还必须将 I-转运到中央滤泡腔内,在那里甲状腺球蛋白被碘化,形成 T4 和 T3 的蛋白质前体。在过去的十年中,有几批证据使得 I-仅通过氯离子/碘离子交换蛋白 Pendrin(SLC26A4)离开甲状腺细胞的观点受到质疑,因此有必要重新考虑其他几个候选 I-通道:氯离子/氢离子反向转运蛋白 CLC-5、囊性纤维化跨膜电导调节因子(CFTR)和单羧酸转运蛋白(SMCT1)。